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US20160108025A1 - Polycyclic herg activators - Google Patents

Polycyclic herg activators Download PDF

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Publication number
US20160108025A1
US20160108025A1 US14/983,741 US201514983741A US2016108025A1 US 20160108025 A1 US20160108025 A1 US 20160108025A1 US 201514983741 A US201514983741 A US 201514983741A US 2016108025 A1 US2016108025 A1 US 2016108025A1
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United States
Prior art keywords
methyl
benzofuran
tetrazol
aniline
trifluoromethyl
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Abandoned
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US14/983,741
Inventor
Gregory Raymond Bebernitz
Emma CODY
Tajesh Patel
Ming Qian
Lewis Whitehead
Thomas ZABAWA
Frederic Zecri
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Novartis AG
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Novartis AG
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Priority to US14/983,741 priority Critical patent/US20160108025A1/en
Publication of US20160108025A1 publication Critical patent/US20160108025A1/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/357—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/357—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
    • A61K31/36—Compounds containing methylenedioxyphenyl groups, e.g. sesamin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/428—Thiazoles condensed with carbocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D307/85—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • Coordinated cardiac contractility is governed by electrical changes that occur in cardiomyocytes.
  • the cardiac impulse or action potential is determined by successive opening and closing of membrane ion channels that regulate the depolarizing (mainly Na + and Ca + ) and repolarizing (mainly K + ) currents (Nerbonne and Kass, 2005). Genetic defects resulting in the malfunctioning of these channels and the associated ionic currents can lead to cardiac rhythm disorders generally described as cardiac channelopathies (Webster and Berul, 2013).
  • LQTS long QT syndrome
  • SCN5A LQT3
  • Cardiac repolarization is primarily mediated by the slow delayed rectifier current, IKs (KCNQ1) and the rapid delayed rectifier current IKr (KCNH2) conducted by the hERG channels (Sanguinetti and Tristani-Firouzi, 2006). Impairment or loss of K + channel function delays cardiac repolarization, leads to excessive prolongation of the action potential duration and associated QT interval in the electrocardiogram and predisposes affected individuals to high risk of developing torsades de pointes arrhythmia and sudden cardiac death (Ravens and Cerbai, 2008).
  • Jervell and Lange-Nielsen syndrome is a rare cause of LQTS characterized by deafness, severe QT prolongation and lethal arrhythmias (Crotti et al. 2008). Most patients die of this disorder as children before age 10 despite aggressive therapy including behavior modification, beta blockers, defibrillators and sympathectomy.
  • This syndrome is caused by homozygous or compound heterozygous mutations in genes KCNQ1 and KCNE1 that are responsible for the delayed rectifier repolarizing current IKs (Crotti et al. 2008).
  • Acquired LQTS is often observed in the setting of structural or functional cardiac disease such as ischemic or diabetic cardiomyopathy. The altered substrate in coronary disease (ischemia or scar) may lower the threshold for afterdepolarization. Thus, subclinical IKs dysfunction with associated reduction in repolarization reserve may be exacerbated in these conditions.
  • hERG channel activators described in the literature include NS1643, NS3623, RPR260243, PD-118057, PD307243, ICA105574, A935142 and KB130015 (Zhou et al., 2011). These compounds act by altering channel activation, inactivation or deactivation (Perry et al. 2010). Pharmacological activation of hERG K + channels is anticipated to normalize the QT interval, functionally mitigate the arrhythmic substrate and consequently reduce cardiac arrhythmia in patients with inherited or acquired LQTS. This approach is likely to be effective in LQTS resulting from mutations in genes other than KCNQ1 since it targets the alteration in QT per se and not specific genetic defects.
  • hERG channel activators may also function as general antiarrhythmics since they reportedly reduce electrical heterogeneity in the myocardium and thereby reduce the possibility of re-entry (Grunnet et al. 2008).
  • the current invention relates to hERG activators useful as pharmaceuticals for the treatment of genetic or acquired long QT syndromes and as a novel class of agents for the treatment of arrhythmias of other etiologies.
  • the invention provides compounds, salts thereof, pharmaceutical formulations thereof and combinations thereof which compounds are hERG activators.
  • the invention further provides methods of treating, preventing, or ameliorating hERG related conditions, comprising administering to a subject in need thereof an effective amount of a hERG modulator (e.g., a compound of the invention).
  • hERG modulators provided herein are compounds of Formula I and salts thereof:
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a therapeutically effective amount of a compound according to the definition of formula (I) or subformulae thereof and one or more pharmaceutically acceptable carriers.
  • the invention provides a combination, in particular a pharmaceutical combination, comprising a therapeutically effective amount of the compound according to the definition of formula (I) or subformulae thereof and one or more therapeutically active ingredients.
  • One embodiment of the invention is to provide a method for treating, preventing, or ameliorating a hERG related condition, comprising administering to a subject in need thereof an effective amount of a hERG modulator of Formula (I), or a pharmaceutical composition comprising the same.
  • the present invention provides compounds that modulate hERG activity. Such compounds may be used in vitro or in vivo to modulate hERG activity in a variety of contexts.
  • the invention provides compounds of Formula I and pharmaceutically acceptable salts thereof, which modulate hERG activity.
  • Compounds of Formula I are represented by the structure, or salt thereof, of formula (I):
  • R 1 is selected from: CO 2 H or tetrazole and R 2 is selected from: H, halo, (C 1 -C 4 )alkyl or halo-substituted(C 1 -C 4 )alkyl, or R 1 is H and R 2 is CO 2 H or tetrazole;
  • X is selected from: H, halo, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, NR 8 R 9 , halo-substituted(C 1 -C 4 )alkyl, phenyl or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said phenyl or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from halo, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substituted(
  • R 3a is selected from: H, (C 1 -C 4 )alkyl or halo-substituted(C 1 -C 4 )alkyl
  • R 3b is selected from: H, (C 1 -C 4 )alkyl or taken together with R 3a forms a 3 to 7 membered saturated cycloalkyl or a 3 to 7 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N
  • R 3c is selected from: H or CH 3
  • R 3d is selected from: H or CH 3
  • R 4 is selected from::
  • R 5 is selected from: H or CH 3 ;
  • R 6 is independently selected from: halo, nitrile, (C 1 -C 4 )alkyl, halo-substituted(C 1 -C 4 )alkyl, nitrile-substituted(C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substituted(C 1 -C 4 )alkoxy, nitrile-substituted(C 1 -C 4 )alkoxy, (C 1 -C 4 )alkylene, N-acetyl, trifluouroacetyl, (C 1 -C 4 )alkylthio, halo-substituted thio, halo-substituted (C 1 -C 4 )alkylthio, (C 3 -C 6 )cycloalkyl, methyla
  • the invention is a compound, or salt thereof, according to the first embodiment, wherein R 1 is selected from: CO 2 H, or tetrazole; R 2 is selected from: H, halo, (C 1 -C 4 )alkyl or halo-substituted(C 1 -C 4 )alkyl; X is selected from: H, halo, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, NR 8 R 9 , halo-substituted(C 1 -C 4 )alkyl, phenyl or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said phenyl or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from halo, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substit
  • R 3a is selected from: H, (C 1 -C 4 )alkyl or halo-substituted(C 1 -C 4 )alkyl
  • R 3b is selected from: H, (C 1 -C 4 )alkyl or taken together with R 3a forms a 3 to 7 membered saturated cycloalkyl or a 3 to 7 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N
  • R 3c is selected from: H or CH 3
  • R 3d is selected from: H or CH 3
  • R 4 is selected from::
  • R 5 is selected from: H or CH 3 ;
  • R 6 is independently selected from: halo, (C 1 -C 4 )alkyl, halo-substituted(C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substituted(C 1 -C 4 )alkoxy, nitrile-substituted(C 1 -C 4 )alkoxy, (C 1 -C 4 )alkylene, N-acetyl, trifluouroacetyl, (C 1 -C 4 )alkylthio, halo-substituted thio, halo-substituted (C 1 -C 4 )alkylthio, (C 3 -C 6 )cycloalkyl, methylamino-substituted(C 1 -C 4 )alkyl, dimethylamino-substituted(C 1 -
  • the invention is the compound, or pharmaceutically acceptable salt thereof, according any one of the preceding embodiments, wherein R 1 is tetrazole.
  • the invention is the compound, or pharmaceutically acceptable salt thereof, according any one of the preceding embodiments, wherein R 2 is hydrogen.
  • the invention is the compound according to the first or secon embodiments, or a salt thereof, wherein the compound is of formula (II):
  • the invention is the compound according to any one of the first through third embodiments, or a salt thereof, wherein the compound is of formula (III):
  • the invention is the compound according to any one of the first through third embodiments, or a salt thereof, wherein the compound is of formula (IV):
  • the invention is the compound according any one of the first through fourth embodiments, or a salt thereof, wherein the compound is of formula (V):
  • the invention is the compound according to any one of the first through fourth or sixth embodiments, or a salt thereof, wherein the compound is of formula (VI):
  • R 2 is selected from: H, CH 3 or CF 3 ;
  • X is selected from: H, halo, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substituted(C 1 -C 4 )alkyl;
  • R 6 is independently selected from: halo, (C 1 -C 4 )alkyl, halo-substituted(C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substituted(C 1 -C 4 )alkoxy; or a pharmaceutically acceptable salt thereof
  • the invention is the compound according to any one of first or second embodiments, or a salt thereof, wherein the compound is of formula (VII):
  • the invention is the compound according to any one of the first, second or eighth embodiments, or a salt thereof, wherein the compound is of formula (VIII):
  • the invention is the compound according to any one of the first, second or eighth embodiments, or a salt thereof, wherein the compound is of formula (IX):
  • the invention is the compound, or salt thereof, according to any one of the first through tenth embodiments, wherein X is selected from: H, halo, (C 1 -C 4 )alkyl, (C 1 -C 4 )alkoxy, halo-substituted(C 1 -C 4 )alkyl; R 3b is H; or a pharmaceutically acceptable salt thereof.
  • the invention is the compound according to the first embodiment, or a salt thereof, wherein the compound is selected from:
  • the invention is the compound according to the first or twelfth embodiments, or a salt thereof, wherein the compound is selected from:
  • the invention is the compound, or salt thereof: N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline.
  • the invention is the compound, or salt thereof: N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline.
  • the invention is a pharmaceutical composition
  • a pharmaceutical composition comprising a therapeutically effective amount of a compound according to any one of the preceding embodiments, or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable carriers.
  • the invention is a combination comprising a therapeutically effective amount of a compound according to any one of the preceding embodiments or a pharmaceutically acceptable salt thereof and one or more therapeutically active co-agents.
  • the invention is a method to treat, prevent or ameliorate a hERG related condition, comprising administering to a subject in need thereof an effective amount of a compound or pharmaceutically acceptable salt thereof of any one of the preceding embodiments.
  • the invention is the method according to the fifteenth embodiment, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • the invention is a compound according to any one of the preceding embodiments, or a pharmaceutically acceptable salt thereof, for use as a medicament.
  • the invention is a compound according to any one of the preceding embodiments, or a pharmaceutically acceptable salt thereof, for use in the treatment of a hERG related condition.
  • the invention is the compound according to the preceding embodiment, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • the invention is the use of a compound according to any one of the preceding embodiments or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of a hERG related condition.
  • the invention is the use of a compound according to the preceding embodiment, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • C 1-4 alkyl refers to a fully saturated branched or unbranched hydrocarbon moiety having 1 to 4 carbon atoms.
  • C 1-6 alkyl and C 1-10 alkyl are to be construed accordingly.
  • C 1-10 alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl, 2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl and n-decyl.
  • C 1-4 alkylene refers to divalent alkyl group as defined herein above having 1 to 4 carbon atoms.
  • C 1-6 alkylene and C 1-10 alkylene are to be construed accordingly.
  • C 1-10 alkylene include, but are not limited to, methylene, ethylene, n-propylene, iso-propylene, n-butylene, sec-butylene, iso-butylene, tert-butylene, n-pentylene, isopentylene, neopentylene, n-hexylene, 3-methylhexylene, 2,2-dimethylpentylene, 2,3-dimethylpentylene, n-heptylene, n-octylene, n-nonylene and n-decylene.
  • halo-substituted(C 1 -C 4 )alkyl refers to a C 1-4 alkyl group as defined herein, wherein at least one of the hydrogen atoms is replaced by a halo atom.
  • the haloC 1-4 alkyl group can be monohaloC 1-4 alkyl, dihaloC 1-4 alkyl or polyhaloC 1-4 alkyl including perhaloC 1-4 alkyl.
  • a monohaloC 1-4 alkyl can have one iodo, bromo, chloro or fluoro within the alkyl group.
  • DihaloC 1-4 alkyl and polyhaloC 1-4 alkyl groups can have two or more of the same halo atoms or a combination of different halo groups within the alkyl.
  • the polyhaloC 1-4 alkyl group contains up to 12, or 10, or 8, or 6, or 4, or 3, or 2 halo groups.
  • Non-limiting examples of haloC 1-4 alkyl include fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl.
  • a perhaloC 1-4 alkyl group refers to a C 1-4 alkyl group having all hydrogen atoms replaced with halo atoms.
  • C 1-4 alkylthio refers to C 1-4 alkyl-S—, wherein C 1-4 alkyl is defined herein above.
  • C 1-6 alkylthio and “C 1-10 alkylthio” are to be construed accordingly.
  • Representative examples of C 1-4 alkylthio include, but are not limited to, methylthio, ethylthio, n-propylthio, iso-propylthio, n-butylthio, sec-butylthio, iso-butylthio and tert-butylthio.
  • haloC 1-4 alkylthio refers to a C 1-4 alkylthio group as defined herein, wherein at least one of the hydrogen atoms is replaced by a halo atom.
  • the haloC 1-4 alkylthio group can be monohaloC 1-4 alkylthio, dihaloC 1-4 alkylthio or polyhaloC 1-4 alkylthio including perhaloC 1-4 alkylthio.
  • a monohaloC 1-4 alkylthio can have one iodo, bromo, chloro or fluoro within the alkylthio group.
  • DihaloC 1-4 alkylthio and polyhaloC 1-4 alkylthio groups can have two or more of the same halo atoms or a combination of different halo groups within the alkylthio.
  • the polyhaloC 1-4 alkylthio group contains up to 8, or 6, or 4, or 3, or 2 halo groups.
  • Non-limiting examples of haloC 1-10 alkylthio include fluoromethylthio, difluoromethylthio, trifluoromethylthio, chloromethylthio, dichloromethylthio, trichloromethylthio, pentafluoroethylthio, heptafluoropropylthio, difluorochloromethylthio, dichlorofluoromethylthio, difluoroethylthio, difluoropropylthio, dichloroethylthio and dichloropropylthio.
  • a perhaloC 1-4 alkylthio group refers to a C 1-10 alkylthio group having all hydrogen atoms replaced with halo atoms.
  • aryl refers to an aromatic hydrocarbon group having 6-20 carbon atoms in the ring portion. Typically, aryl is monocyclic, bicyclic or tricyclic aryl having 6-20 carbon atoms and includes one or more aromatic rings fused to one or more non-aromatic hydrocarbon rings. Non-limiting examples include phenyl, naphthyl or tetrahydronaphthyl.
  • C 1-4 alkoxy or “C 1-4 alkoxyl” refers to C 1-4 alkyl-O—, wherein C 1-4 alkyl is defined herein above.
  • Representative examples of C 1-4 alkoxy include, but are not limited to, methoxy, ethoxy, propoxy, 2-propoxy, butoxy and tert-butoxy.
  • halo-substituted(C 1 -C 4 )alkoxy refers to a C 1-4 alkoxy group as defined herein, wherein at least one of the hydrogen atoms is replaced by a halo atom.
  • the haloC 1-4 alkoxy group can be monohaloC 1-4 alkoxy, dihaloC 1-4 alkoxy or polyhaloC 1-4 alkoxy including perhaloC 1-4 alkoxy.
  • a monohaloC 1-4 alkoxy can have one iodo, bromo, chloro or fluoro within the alkoxy group.
  • DihaloC 1-4 alkoxy and polyhaloC 1-4 alkoxy groups can have two or more of the same halo atoms or a combination of different halo groups within the alkoxy.
  • the polyhaloC 1-4 alkoxy group contains up to 8, or 6, or 4, or 3, or 2 halo groups.
  • Non-limiting examples of haloC 1-4 alkyl include fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy, trichloromethoxy, pentafluoroethoxy, heptafluoropropoxy, difluorochloromethoxy, dichlorofluoromethoxy, difluoroethoxy, difluoropropoxy, dichloroethoxy and dichloropropoxy.
  • a perhaloC 1-4 alkoxy group refers to a C 1-4 alkoxy group having all hydrogen atoms replaced with halo atoms.
  • heterocyclyl or “heterocyclo” refers to a saturated or unsaturated non-aromatic ring or ring system, which is a 4-, 5-, 6-, or 7-membered monocyclic ring containing 1, 2 or 3 heteroatoms selected from O, S and N, a 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring system containing 1, 2, 3, 4 or 5 heteroatoms selected from O, S and N, or a 10-, 11-, 12-, 13-, 14- or 15-membered tricyclic ring system and containing 1, 2, 3, 4, 5, 6 or 7 heteroatoms selected from O, S and N, where the N and S can also optionally be oxidized to various oxidation states.
  • the heterocyclic group can be attached via a heteroatom or a carbon atom.
  • the heterocyclyl can include fused or bridged rings as well as spirocyclic rings.
  • heterocycles include tetrahydrofuran (THF), dihydrofuran, 1,4-dioxane, morpholine, 1,4-dithiane, piperazine, piperidine, 1,3-dioxolane, imidazolidine, imidazoline, pyrroline, pyrrolidine, tetrahydropyran, dihydropyran, oxathiolane, dithiolane, 1,3-dioxane, 1,3-dithiane, oxathiane and thiomorpholine.
  • THF tetrahydrofuran
  • dihydrofuran 1,4-dioxane
  • morpholine 1,4-dithiane
  • piperazine piperidine
  • 1,3-dioxolane imid
  • C 3-6 cycloalkyl refers to saturated or unsaturated monocyclic, bicyclic or tricyclic hydrocarbon groups of 3-6 carbon atoms.
  • C 3-6 cycloalkyl refers to a fully saturated or unsaturated monocyclic hydrocarbon group of 3-8 carbon atoms.
  • Exemplary monocyclic hydrocarbon groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl and cyclohexenyl.
  • heteroaryl refers to a 5-, 6-, or 7-membered monocyclic aromatic ring containing 1, 2, 3 or 4 heteroatoms selected from O, S and N, an 8-, 9-, or 10-membered fused bicyclic ring system containing 1, 2, 3, 4 or 5 heteroatoms selected from O, S and N, or an 11-, 12-, 13-, or 14-membered fused tricyclic ring system containing 1, 2, 3, 4, 5 or 6 heteroatoms selected from O, S and N, wherein at least one of the rings of the bicyclic or tricyclic ring systems is fully aromatic.
  • Typical heteroaryl groups include 2- or 3-thienyl, 2- or 3-furyl, 2- or 3-pyrrolyl, 2-, 4-, or 5-imidazolyl, 3-, 4-, or 5-pyrazolyl, 2-, 4-, or 5-thiazolyl, 3-, 4-, or 5-isothiazolyl, 2-, 4-, or 5-oxazolyl, 3-, 4-, or 5-isoxazolyl, 3- or 5-1,2,4-triazolyl, 4- or 5-1,2,3-triazolyl, tetrazolyl, 2-, 3-, or 4-pyridyl, 3- or 4-pyridazinyl, 3-, 4-, or 5-pyrazinyl, 2-pyrazinyl, 2-, 4-, or 5-pyrimidinyl, 1-, 2-, 3-, 5-, 6-, 7-, or 8-indolizinyl, 1-, 3-, 4-, 5-, 6-, or 7-isoindolyl, 2-, 3-, 4-, 5-, 6-, or 7-indolyl, 2-
  • tetrazole refers to both 1-tetrazole and 2-tetrazole, i.e.
  • halogen refers to fluoro, chloro, bromo, and iodo.
  • the term “isomers” refers to different compounds that have the same molecular formula but differ in arrangement and configuration of the atoms, e.g. 1-tetrazole and 2-tetrazole are inseparable isomers.
  • an optical isomer or “a stereoisomer” refers to any of the various stereo isomeric configurations which may exist for a given compound of the present invention and includes geometric isomers. It is understood that a substituent may be attached at a chiral center of a carbon atom. Therefore, the invention includes enantiomers, diastereomers or racemates of the compound.
  • Enantiomers are a pair of stereoisomers that are non-superimposable mirror images of each other. A 1:1 mixture of a pair of enantiomers is a “racemic” mixture. The term is used to designate a racemic mixture where appropriate.
  • “Diastereoisomers” are stereoisomers that have at least two asymmetric atoms, but which are not mirror-images of each other. The absolute stereochemistry is specified according to the Cahn-Ingold-Prelog R-S system. When a compound is a pure enantiomer the stereochemistry at each chiral carbon may be specified by either R or S.
  • Resolved compounds whose absolute configuration is unknown can be designated (+) or ( ⁇ ) depending on the direction (dextro- or levorotatory) which they rotate plane polarized light at the wavelength of the sodium D line.
  • Certain of the compounds described herein contain one or more asymmetric centers or axes and may thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)-.
  • the present invention is meant to include all such possible isomers, including racemic mixtures, optically pure forms and intermediate mixtures.
  • Optically active (R)- and (S)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques.
  • the substituent may be E or Z configuration. If the compound contains a disubstituted cycloalkyl, the cycloalkyl substituent may have a cis- or trans-configuration. All tautomeric forms are also intended to be included.
  • salt refers to an acid addition or base addition salt of a compound of the invention.
  • Salts include in particular “pharmaceutical acceptable salts.”
  • pharmaceutically acceptable salts refers to salts that retain the biological effectiveness and properties of the compounds of this invention and, which typically are not biologically or otherwise undesirable.
  • the compounds of the present invention are capable of forming acid and/or base salts by virtue of the presence of amino and/or carboxyl groups or groups similar thereto.
  • Pharmaceutically acceptable acid addition salts can be formed with inorganic acids and organic acids, e.g., acetate, aspartate, benzoate, besylate, bromide/hydrobromide, bicarbonate/carbonate, bisulfate/sulfate, camphorsulfornate, chloride/hydrochloride, chlortheophyllonate, citrate, ethandisulfonate, fumarate, gluceptate, gluconate, glucuronate, hippurate, hydroiodide/iodide, isethionate, lactate, lactobionate, laurylsulfate, malate, maleate, malonate, mandelate, mesylate, methylsulphate, naphthoate, napsylate, nicotinate, nitrate, octadecanoate, oleate, oxalate, palmitate, pamoate, phosphate/hydrogen phosphate/di hydrogen
  • Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like.
  • Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, sulfosalicylic acid, and the like.
  • Pharmaceutically acceptable base addition salts can be formed with inorganic and organic bases.
  • Inorganic bases from which salts can be derived include, for example, ammonium salts and metals from columns I to XII of the periodic table.
  • the salts are derived from sodium, potassium, ammonium, calcium, magnesium, iron, silver, zinc, and copper; particularly suitable salts include ammonium, potassium, sodium, calcium and magnesium salts.
  • Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines, basic ion exchange resins, and the like.
  • Certain organic amines include isopropylamine, benzathine, cholinate, diethanolamine, diethylamine, lysine, meglumine, piperazine and tromethamine.
  • the pharmaceutically acceptable salts of the present invention can be synthesized from a parent compound, a basic or acidic moiety, by conventional chemical methods.
  • such salts can be prepared by reacting free acid forms of these compounds with a stoichiometric amount of the appropriate base (such as Na, Ca, Mg, or K hydroxide, carbonate, bicarbonate or the like), or by reacting free base forms of these compounds with a stoichiometric amount of the appropriate acid.
  • a stoichiometric amount of the appropriate base such as Na, Ca, Mg, or K hydroxide, carbonate, bicarbonate or the like
  • Such reactions are typically carried out in water or in an organic solvent, or in a mixture of the two.
  • use of non-aqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile is desirable, where practicable.
  • any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds.
  • Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number.
  • isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, and chlorine, such as 2 H, 3 H, 11 C, 13 C, 14 C, 15 N, 18 F 31 P, 32 P, 35 S, 36 Cl, 125 I respectively.
  • the invention includes various isotopically labeled compounds as defined herein, for example those into which radioactive isotopes, such as 3 H, 13 C, and 14 C, are present.
  • isotopically labelled compounds are useful in metabolic studies (with 14 C), reaction kinetic studies (with, for example 2 H or 3 H), detection or imaging techniques, such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT) including drug or substrate tissue distribution assays, or in radioactive treatment of patients.
  • PET positron emission tomography
  • SPECT single-photon emission computed tomography
  • an 18 F or labeled compound may be particularly desirable for PET or SPECT studies.
  • Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.
  • isotopic enrichment factor means the ratio between the isotopic abundance and the natural abundance of a specified isotope.
  • a substituent in a compound of this invention is denoted deuterium, such compound has an isotopic enrichment factor for each designated deuterium atom of at least 3500 (52.5% deuterium incorporation at each designated deuterium atom), at least 4000 (60% deuterium incorporation), at least 4500 (67.5% deuterium incorporation), at least 5000 (75% deuterium incorporation), at least 5500 (82.5% deuterium incorporation), at least 6000 (90% deuterium incorporation), at least 6333.3 (95% deuterium incorporation), at least 6466.7 (97% deuterium incorporation), at least 6600 (99% deuterium incorporation), or at least 6633.3 (99.5% deuterium incorporation).
  • Isotopically-labeled compounds of formula (I) can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying Examples and Preparations using an appropriate isotopically-labeled reagents in place of the non-labeled reagent previously employed.
  • solvates in accordance with the invention include those wherein the solvent of crystallization may be isotopically substituted, e.g., D 2 O, d 6 -acetone, d 6 -DMSO.
  • Compounds of the invention i.e. compounds of formula (I) that contain groups capable of acting as donors and/or acceptors for hydrogen bonds may be capable of forming co-crystals with suitable co-crystal formers.
  • These co-crystals may be prepared from compounds of formula (I) by known co-crystal forming procedures. Such procedures include grinding, heating, co-subliming, co-melting, or contacting in solution compounds of formula (I) with the co-crystal former under crystallization conditions and isolating co-crystals thereby formed.
  • Suitable co-crystal formers include those described in WO 2004/078163.
  • the invention further provides co-crystals comprising a compound of formula (I).
  • a therapeutically effective amount of a compound of the present invention refers to an amount of the compound of the present invention that will elicit the biological or medical response of a subject, for example, reduction or inhibition of an enzyme or a protein activity, or ameliorate symptoms, alleviate conditions, slow or delay disease progression, or prevent a disease, etc.
  • the term “a therapeutically effective amount” refers to the amount of the compound of the present invention that, when administered to a subject, is effective to (1) at least partially alleviate, inhibit, prevent and/or ameliorate a condition, or a disorder or a disease mediated by hERG; or (2) activating the activity of hERG.
  • a therapeutically effective amount refers to the amount of the compound of the present invention that, when administered to a cell, or a tissue, or a non-cellular biological material, or a medium, is effective to at least partially activating the activity of hERG; or at least partially activating the expression of hERG.
  • therapeutically effective amount and “effective amount” are used herein to mean an amount sufficient to reduce by at least about 15 percent, preferably by at least 50 percent, more preferably by at least 90 percent, and most preferably prevent, a clinically significant deficit in the activity, function and response of the host. Alternatively, a therapeutically effective amount is sufficient to cause an improvement in a clinically significant condition/symptom in the host.
  • the effective amount can vary depending on such factors as the size and weight of the subject, the type of illness, or the particular compound of the invention. For example, the choice of the compound of the invention can affect what constitutes an “effective amount.”
  • One of ordinary skill in the art would be able to study the factors contained herein and make the determination regarding the effective amount of the compounds of the invention without undue experimentation.
  • the regimen of administration can affect what constitutes an effective amount.
  • the compound of the invention can be administered to the subject either prior to or after the onset of a hERG related condition. Further, several divided dosages, as well as staggered dosages, can be administered daily or sequentially, or the dose can be continuously infused, or can be a bolus injection. Further, the dosages of the compound(s) of the invention can be proportionally increased or decreased as indicated by the exigencies of the therapeutic or prophylactic situation.
  • the term “subject” refers to an animal. Typically the animal is a mammal. A subject also refers to for example, primates (e.g., humans, male or female), cows, sheep, goats, horses, dogs, cats, rabbits, rats, mice, fish, birds and the like. In certain embodiments, the subject is a primate. In yet other embodiments, the subject is a human.
  • primates e.g., humans, male or female
  • the subject is a primate.
  • the subject is a human.
  • the term “inhibit”, “inhibition” or “inhibiting” refers to the reduction or suppression of a given condition, symptom, or disorder, or disease, or a significant decrease in the baseline activity of a biological activity or process.
  • the term “treat”, “treating” or “treatment” of any disease or disorder refers in one embodiment, to ameliorating the disease or disorder (i.e., slowing or arresting or reducing the development of the disease or at least one of the clinical symptoms thereof).
  • “treat,” “treating,” or “treatment” refers to alleviating or ameliorating at least one physical parameter including those which may not be discernible by the patient.
  • “treat”, “treating” or “treatment” refers to modulating the disease or disorder, either physically (e.g., through stabilization of a discernible symptom), physiologically, (e.g., through stabilization of a physical parameter), or both.
  • “treat,” “treating,” or “treatment” refers to preventing or delaying the onset or development or progression of the disease or disorder.
  • a subject is “in need of” a treatment if such subject would benefit biologically, medically or in quality of life from such treatment.
  • any asymmetric atom (e.g., carbon or the like) of the compound(s) of the present invention can be present in racemic or enantiomerically enriched, for example the (R)-, (S)- or (R,S)-configuration.
  • each asymmetric atom has at least 50% enantiomeric excess, at least 60% enantiomeric excess, at least 70% enantiomeric excess, at least 80% enantiomeric excess, at least 90% enantiomeric excess, at least 95% enantiomeric excess, or at least 99% enantiomeric excess in the (R)- or (S)-configuration.
  • Substituents at atoms with unsaturated bonds may, if possible, be present in cis-(Z)- or trans-(E)-form.
  • a compound of the present invention can be in the form of one of the possible isomers, rotamers, atropisomers, tautomers or mixtures thereof, for example, as substantially pure geometric (cis or trans) isomers, diastereomers, optical isomers (antipodes), racemates or mixtures thereof.
  • Any resulting mixtures of isomers can be separated on the basis of the physicochemical differences of the constituents, into the pure or substantially pure geometric or optical isomers, diastereomers, racemates, for example, by chromatography and/or fractional crystallization.
  • any resulting racemates of final products or intermediates can be resolved into the optical antipodes by known methods, e.g., by separation of the diastereomeric salts thereof, obtained with an optically active acid or base, and liberating the optically active acidic or basic compound.
  • a basic moiety may thus be employed to resolve the compounds of the present invention into their optical antipodes, e.g., by fractional crystallization of a salt formed with an optically active acid, e.g., tartaric acid, dibenzoyl tartaric acid, diacetyl tartaric acid, di-O,O′-p-toluoyl tartaric acid, mandelic acid, malic acid or camphor-10-sulfonic acid.
  • Racemic products can also be resolved by chiral chromatography, e.g., high pressure liquid chromatography (HPLC) using a chiral adsorbent.
  • HPLC high pressure liquid chromatography
  • the compounds of the present invention may also form internal salts, e.g., zwitterionic molecules.
  • the compounds of the present invention can also be obtained in the form of their hydrates, or include other solvents used for their crystallization.
  • the compounds of the present invention may inherently or by design form solvates with pharmaceutically acceptable solvents (including water); therefore, it is intended that the invention embrace both solvated and unsolvated forms.
  • solvate refers to a molecular complex of a compound of the present invention (including pharmaceutically acceptable salts thereof) with one or more solvent molecules.
  • solvent molecules are those commonly used in the pharmaceutical art, which are known to be innocuous to the recipient, e.g., water, ethanol, and the like.
  • hydrate refers to the complex where the solvent molecule is water.
  • the compounds of the present invention including salts, hydrates and solvates thereof, may inherently or by design form polymorphs.
  • the invention further includes any variant of the present processes, in which an intermediate product obtainable at any stage thereof is used as starting material and the remaining steps are carried out, or in which the starting materials are formed in situ under the reaction conditions, or in which the reaction components are used in the form of their salts or optically pure material.
  • the present invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of the present invention, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
  • the pharmaceutical composition can be formulated for particular routes of administration such as oral administration, parenteral administration, and rectal administration, etc.
  • the pharmaceutical compositions of the present invention can be made up in a solid form (including without limitation capsules, tablets, pills, granules, powders or suppositories), or in a liquid form (including without limitation solutions, suspensions or emulsions).
  • compositions can be subjected to conventional pharmaceutical operations such as sterilization and/or can contain conventional inert diluents, lubricating agents, or buffering agents, as well as adjuvants, such as preservatives, stabilizers, wetting agents, emulsifers and buffers, etc.
  • the pharmaceutical compositions are tablets or gelatin capsules comprising the active ingredient together with
  • diluents e.g., lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and/or glycine;
  • lubricants e.g., silica, talcum, stearic acid, its magnesium or calcium salt and/or polyethyleneglycol; for tablets also
  • lubricants e.g., silica, talcum, stearic acid, its magnesium or calcium salt and/or polyethyleneglycol
  • binders e.g., magnesium aluminum silicate, starch paste, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone; if desired
  • disintegrants e.g., starches, agar, alginic acid or its sodium salt, or effervescent mixtures; and/or
  • Tablets may be either film coated or enteric coated according to methods known in the art.
  • compositions for oral administration include an effective amount of a compound of the invention in the form of tablets, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsion, hard or soft capsules, or syrups or elixirs.
  • Compositions intended for oral use are prepared according to any method known in the art for the manufacture of pharmaceutical compositions and such compositions can contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide pharmaceutically elegant and palatable preparations. Tablets may contain the active ingredient in admixture with nontoxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets.
  • excipients are, for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example, starch, gelatin or acacia; and lubricating agents, for example magnesium stearate, stearic acid or talc.
  • the tablets are uncoated or coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period.
  • a time delay material such as glyceryl monostearate or glyceryl distearate can be employed.
  • Formulations for oral use can be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example, peanut oil, liquid paraffin or olive oil.
  • an inert solid diluent for example, calcium carbonate, calcium phosphate or kaolin
  • water or an oil medium for example, peanut oil, liquid paraffin or olive oil.
  • compositions are aqueous isotonic solutions or suspensions, and suppositories are advantageously prepared from fatty emulsions or suspensions.
  • Said compositions may be sterilized and/or contain adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure and/or buffers. In addition, they may also contain other therapeutically valuable substances.
  • Said compositions are prepared according to conventional mixing, granulating or coating methods, respectively, and contain about 0.1-75%, or contain about 1-50%, of the active ingredient.
  • Anhydrous pharmaceutical compositions and dosage forms of the invention can be prepared using anhydrous or low moisture containing ingredients and low moisture or low humidity conditions.
  • An anhydrous pharmaceutical composition may be prepared and stored such that its anhydrous nature is maintained. Accordingly, anhydrous compositions are packaged using materials known to prevent exposure to water such that they can be included in suitable formulary kits. Examples of suitable packaging include, but are not limited to, hermetically sealed foils, plastics, unit dose containers (e.g., vials), blister packs, and strip packs.
  • compositions and dosage forms that comprise one or more agents that reduce the rate by which the compound of the present invention as an active ingredient will decompose.
  • agents which are referred to herein as “stabilizers,” include, but are not limited to, antioxidants such as ascorbic acid, pH buffers, or salt buffers, etc.
  • the compounds of formula I in free form or in salt form exhibit valuable pharmacological properties, e.g., as indicated in in vitro tests as provided in the next sections, and are therefore indicated for therapy or for use as research chemicals, e.g., as tool compounds.
  • the present invention provides the use of a compound of formula (I) or a salt thereof in therapy.
  • the therapy is selected from a disease which may be treated by modulating hERG protein production.
  • the disease is selected from the afore-mentioned list, e.g., LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • the invention provides a method of treating a disease which is treated by modulating hERG protein production comprising administration of a therapeutically acceptable amount of a compound of formula (I) or salt thereof to a patient in need of such therapy.
  • the disease is selected from the afore-mentioned list, suitably LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • the present invention provides the use of a compound of formula (I) or salt thereof for the manufacture of a medicament.
  • the medicament is for treatment of a disease which may be treated by modulation of hERG protein production.
  • the disease is selected from the afore-mentioned list, suitably LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • the pharmaceutical composition or combination of the present invention can be in unit dosage of about 1-1000 mg of active ingredient(s) for a subject of about 50-70 kg, or about 1-500 mg or about 1-250 mg or about 1-150 mg or about 0.5-100 mg, or about 1-50 mg of active ingredients.
  • the therapeutically effective dosage of a compound, the pharmaceutical composition, or the combinations thereof is dependent on the species of the subject, the body weight, age and individual condition, the disorder or disease or the severity thereof being treated. A physician, clinician or veterinarian of ordinary skill can readily determine the effective amount of each of the active ingredients necessary to prevent, treat or inhibit the progress of the disorder or disease.
  • the above-cited dosage properties are demonstrable in vitro and in vivo tests using advantageously mammals, e.g., mice, rats, dogs, monkeys or isolated organs, tissues and preparations thereof.
  • the compounds of the present invention can be applied in vitro in the form of solutions, e.g., aqueous solutions, and in vivo either enterally, parenterally, advantageously intravenously, e.g., as a suspension or in aqueous solution.
  • the dosage in vitro may range between about 10 ⁇ 3 molar and 10 ⁇ 9 molar concentrations.
  • a therapeutically effective amount in vivo may range depending on the route of administration, between about 0.1-500 mg/kg, or between about 1-100 mg/kg.
  • the compound of the present invention may be administered either simultaneously with, or before or after, one or more other therapeutic agent.
  • the compound of the present invention may be administered separately, by the same or different route of administration, or together in the same pharmaceutical composition as the other agents.
  • the invention provides a product comprising a compound of formula (I) and at least one other therapeutic agent as a combined preparation for simultaneous, separate or sequential use in therapy.
  • the therapy is the treatment of a spinal muscular atrophy.
  • Products provided as a combined preparation include a composition comprising the compound of formula (I) and the other therapeutic agent(s) together in the same pharmaceutical composition, or the compound of formula (I) and the other therapeutic agent(s) in separate form, e.g., in the form of a kit.
  • the invention provides a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of formula (I) and another therapeutic agent(s).
  • the pharmaceutical composition may comprise a pharmaceutically acceptable carrier, as described above.
  • the invention provides a kit comprising two or more separate pharmaceutical compositions, at least one of which contains a compound of formula (I).
  • the kit comprises means for separately retaining said compositions, such as a container, divided bottle, or divided foil packet.
  • a container, divided bottle, or divided foil packet An example of such a kit is a blister pack, as typically used for the packaging of tablets, capsules and the like.
  • the kit of the invention may be used for administering different dosage forms, for example, oral and parenteral, for administering the separate compositions at different dosage intervals, or for titrating the separate compositions against one another.
  • the kit of the invention typically comprises directions for administration.
  • the compound of the invention and the other therapeutic agent may be manufactured and/or formulated by the same or different manufacturers. Moreover, the compound of the invention and the other therapeutic may be brought together into a combination therapy: (i) prior to release of the combination product to physicians (e.g., in the case of a kit comprising the compound of the invention and the other therapeutic agent); (ii) by the physician themselves (or under the guidance of the physician) shortly before administration; (iii) in the patient themselves, e.g., during sequential administration of the compound of the invention and the other therapeutic agent.
  • the retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 ⁇ m, 2.1 ⁇ 50 mm column. A gradient of H 2 O (+0.1% formic acid)/CH 3 CN (+0.1% formic acid) 95/5 to 5/95 was applied over 1.2 min., then held for 0.5 min. (1.0 mL/min. as solvent flow) at an oven temperature of 50° C.
  • the retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 ⁇ m, 3.0 ⁇ 30 mm column. A gradient of H 2 O (+5 mM ammonium hydroxide)/CH 3 CN 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
  • the retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 ⁇ m, 3.0 ⁇ 30 mm column. A gradient of H 2 O (+5 mM ammonium hydroxide)/CH 3 CN 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
  • the present invention also includes processes for the preparation of compounds of the invention.
  • reactive functional groups for example hydroxy, amino, imino, thio or carboxy groups, where these are desired in the final product, to avoid their unwanted participation in the reactions.
  • Conventional protecting groups can be used in accordance with standard practice, for example, see T. W. Greene and P. G. M. Wuts in “Protective Groups in Organic Chemistry”, John Wiley and Sons, 1991.
  • the reaction was then heated to 120° C. for 18 hr. After 18 hr the rxn was cooled to RT and diluted with EtOAc. The reaction mixture was filtered through a silica plug to remove solids and flushed with EtOAc. The collected filtrates were diluted with water and brine and extracted with EtOAc ⁇ 2. The combined organic layers were washed with brine, dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure. The crude mixture was purified via silica gel FCC, 100% Heptane—20% EtOAc/80% Heptane to give a yellow solid, 6-methylbenzofuran-2-carbonitrile (5.1 g).
  • 6-methylbenzofuran-2-carbonitrile (12 g, 76 mmol), NBS (13.59 g, 76 mmol), and AIBN (1.25 g, 7.64 mmol) were dissolved in carbon tetrachloride (191 ml). The mixture was heated to reflux overnight. After 18 h the reaction was cooled to RT and concentrated under reduced pressure. The product was then crashed out using MeOH and the slurry was placed in the fridge overnight. The slurry was filtered and the collected PPT was washed with MeOH. The collected PPT was pure 6-(bromomethyl)benzofuran-2-carbonitrile (13.864 g).
  • Step 7 Synthesis of N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline
  • Methyl 6-(bromomethyl)benzofuran-2-carboxylate was prepared as described in general bromination procedure, example 37, Step 5, starting from methyl 6-methylbenzofuran-2-carboxylate.
  • Step 3 Synthesis of 5-fluoro-6-(((4-(trifluoromethoxy)-3-(trifluoromethyl)phenyl)amino)-methyl)benzofuran-2-carbonitrile
  • Step 4 Synthesis of N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline
  • Step 1 Synthesis of ethyl 2-(2-formyl-4-methylphenoxy)acetate
  • Trimethlamine-N-oxide (6.75 g, 90 mmol) was added to a solution of 5-(bromomethyl)benzofuran-2-carbonitrile (4.46 g, 18.89 mmol) in 57 mL of DMSO and 6 mL of H 2 O. The mixture was stirred at 70° C. for 3 hr. After the reaction was cooled to room temperature, the mixture was diluted with 72 mL of brine, and extracted with EtOAc (3 ⁇ 100 mL). The combined organic layers were washed with H 2 O (2 ⁇ 20 mL), brine, dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure.
  • Step 1 Synthesis of methyl 6-bromo-3-methylbenzofuran-2-carboxylate
  • Step 7 Synthesis of 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-3-methylbenzofuran-2-carbonitrile
  • Step 2 Synthesis of ethyl 2-(5-methyl-2-(2,2,2-trifluoroacetyl)phenoxy)acetate
  • Step 3 Synthesis of ethyl 6-methyl-3-(trifluoromethyl)benzofuran-2-carboxylate
  • Step 3 Synthesis of ( ⁇ ) 5-(1-((3-chloro-4-propylphenyl)amino)ethyl)benzofuran-2-carbonitrile
  • the separated organic layer was washed with H 2 O, brine and dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure.
  • the residue was dissolved in 1.4 mL of TFE and NaBH 4 (15.69 mg, 0.415 mmol) was added.
  • the reaction was stirred at 40° C. for 2 hr. After cooling to room temperature, the reaction mixture was diluted with 50 mL of DCM, which was then washed with H 2 O, brine, dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure.
  • Step 1 Synthesis of ethyl 5-formyl-3-methylbenzofuran-2-carboxylate
  • the crude mixture was diluted with EtOAc and Water. The organic layer was washed with water and brine, dried over Na 2 SO 4 , filtered and concentrated under reduced pressure. The crude was diluted with DCM and silica gel was added. The mixture was concentrated under reduced pressure to dry-load material for purification. The crude was purified via silica gel FCC, 100% Heptane—100% EtOAc to give 4-nitro-2-(prop-1-en-2-yl)-1-(trifluoromethoxy)benzene (456 mg).
  • a patch-clamp assay on the QPatch ⁇ automated patch clamp system was employed to assesses whether compounds functionally enhance the cardiac delayed rectifier hERG (human ether-a-go-go-related gene) potassium channel.
  • the assay measures electric the current passing through hERG channels that are heterologously expressed in a stable Chinese hamster ovary (CHO) cell line. Channels are opened by a hERG-specific voltage protocol and the compound effect is directly characterized by the activation of the hERG current.
  • EC 50 values are obtained from fitting 4-concentration dose response curves (1.1, 3.3, 10 & 30 uM) in triplicates at 4 different sections of the voltage protocol (steady state current amplitude at +10 mV, at +30 mV, peak tail current amplitude and tail current amplitude at 7 second). In the absence of a clear trend of saturation at 30 uM, only increased % current values for the 4 parameters are utilized.

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Abstract

The present invention provides a compound of formula I, in which R1, R2, X and R3 are defined in the Summary of the Invention, or a pharmaceutically acceptable salt thereof;
Figure US20160108025A1-20160421-C00001
a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

Description

    BACKGROUND OF THE INVENTION
  • Coordinated cardiac contractility is governed by electrical changes that occur in cardiomyocytes. The cardiac impulse or action potential is determined by successive opening and closing of membrane ion channels that regulate the depolarizing (mainly Na+ and Ca+) and repolarizing (mainly K+) currents (Nerbonne and Kass, 2005). Genetic defects resulting in the malfunctioning of these channels and the associated ionic currents can lead to cardiac rhythm disorders generally described as cardiac channelopathies (Webster and Berul, 2013). Inherited mutations in cardiac ion channels resulting in gain or loss of channel function can alter the atrial and ventricular action potential and cause various cardiac arrhythmia syndromes, including long QT syndrome (LQTS), short QT syndrome, Brugada syndrome, and familial atrial fibrillation (Giudicessi and Ackerman, 2012). Prolongation of QT interval caused by abnormal cardiac repolarization is associated with an increased risk of life-threatening tachyarrhythmia. Presently 16 genes associated with LQTS have been identified with differing signs and symptoms, depending on the locus involved. The majority of cases have mutations in the KCNQ1 (LQT1), KCNH2 (LQT2) and SCN5A (LQT3) genes (Schwartz et al. 2013).
  • Cardiac repolarization is primarily mediated by the slow delayed rectifier current, IKs (KCNQ1) and the rapid delayed rectifier current IKr (KCNH2) conducted by the hERG channels (Sanguinetti and Tristani-Firouzi, 2006). Impairment or loss of K+ channel function delays cardiac repolarization, leads to excessive prolongation of the action potential duration and associated QT interval in the electrocardiogram and predisposes affected individuals to high risk of developing torsades de pointes arrhythmia and sudden cardiac death (Ravens and Cerbai, 2008). Jervell and Lange-Nielsen syndrome (JLN) is a rare cause of LQTS characterized by deafness, severe QT prolongation and lethal arrhythmias (Crotti et al. 2008). Most patients die of this disorder as children before age 10 despite aggressive therapy including behavior modification, beta blockers, defibrillators and sympathectomy. This syndrome is caused by homozygous or compound heterozygous mutations in genes KCNQ1 and KCNE1 that are responsible for the delayed rectifier repolarizing current IKs (Crotti et al. 2008). Acquired LQTS is often observed in the setting of structural or functional cardiac disease such as ischemic or diabetic cardiomyopathy. The altered substrate in coronary disease (ischemia or scar) may lower the threshold for afterdepolarization. Thus, subclinical IKs dysfunction with associated reduction in repolarization reserve may be exacerbated in these conditions.
  • hERG channel activators described in the literature include NS1643, NS3623, RPR260243, PD-118057, PD307243, ICA105574, A935142 and KB130015 (Zhou et al., 2011). These compounds act by altering channel activation, inactivation or deactivation (Perry et al. 2010). Pharmacological activation of hERG K+ channels is anticipated to normalize the QT interval, functionally mitigate the arrhythmic substrate and consequently reduce cardiac arrhythmia in patients with inherited or acquired LQTS. This approach is likely to be effective in LQTS resulting from mutations in genes other than KCNQ1 since it targets the alteration in QT per se and not specific genetic defects. hERG channel activators may also function as general antiarrhythmics since they reportedly reduce electrical heterogeneity in the myocardium and thereby reduce the possibility of re-entry (Grunnet et al. 2008). Thus, the current invention relates to hERG activators useful as pharmaceuticals for the treatment of genetic or acquired long QT syndromes and as a novel class of agents for the treatment of arrhythmias of other etiologies.
    • 1. Nerbonne J M, Kass R S. Molecular physiology of cardiac repolarization. Physiol Rev. 2005; 85:1205-53.
    • 2. Webster G, Berul C I. An update on channelopathies: from mechanisms to management. Circulation. 2013; 127:126-40.
    • 3. Giudicessi, J. R. & Ackerman, M. J. Potassium-channel mutations and cardiac arrhythmias-diagnosis and therapy. Nat Rev Cardiol. 2012; 9:319-32.
    • 4. Schwartz P J, Ackerman M J, George A L Jr, Wilde A A. Impact of Genetics on the Clinical Management of Channelopathies. J Am Coil Cardiol. 2013 May 15 (Epub ahead of print)
    • 5. Sanguinetti M C, Tristani-Firouzi M. hERG potassium channels and cardiac arrhythmia. Nature. 2006; 440:463-9.
    • 6. Ravens U, Cerbai E. Role of potassium currents in cardiac arrhythmias. Europace. 2008; 10:1133-7.
    • 7. Crotti L, Celano G, Dagradi F, Schwartz P J. Congenital long Q T syndrome. Orphanet J Rare Dis. 2008; 3:18.
    • 8. Zhou P Z, Babcock J, Liu L Q, Li M, Gao Z B. Activation of human ether-a-go-go related gene (hERG) potassium channels by small molecules. Acta Pharmacol Sin. 2011; 32:781-8.
    • 9. Perry M, Sanguinetti M, Mitcheson J. Revealing the structural basis of action of hERG potassium channel activators and blockers. J Physiol. 2010; 588(Pt 17):3157-67.
    • 10. Grunnet M, Hansen R S, Olesen S P. hERG1 channel activators: a new anti-arrhythmic principle. Prog Biophys Mol Biol. 2008; 98:347-62.
    SUMMARY OF THE INVENTION
  • There remains a need for new compounds that activate hERG. The invention provides compounds, salts thereof, pharmaceutical formulations thereof and combinations thereof which compounds are hERG activators. The invention further provides methods of treating, preventing, or ameliorating hERG related conditions, comprising administering to a subject in need thereof an effective amount of a hERG modulator (e.g., a compound of the invention).
  • Various embodiments of the invention are described herein. It will be recognized that features specified in each embodiment may be combined with other specified features to provide further embodiments.
  • Within certain aspects, hERG modulators provided herein are compounds of Formula I and salts thereof:
  • Figure US20160108025A1-20160421-C00002
  • In another embodiment, the invention provides a pharmaceutical composition comprising a therapeutically effective amount of a compound according to the definition of formula (I) or subformulae thereof and one or more pharmaceutically acceptable carriers.
  • In another embodiment, the invention provides a combination, in particular a pharmaceutical combination, comprising a therapeutically effective amount of the compound according to the definition of formula (I) or subformulae thereof and one or more therapeutically active ingredients.
  • One embodiment of the invention is to provide a method for treating, preventing, or ameliorating a hERG related condition, comprising administering to a subject in need thereof an effective amount of a hERG modulator of Formula (I), or a pharmaceutical composition comprising the same.
    • DETAILED DESCRIPTION OF THE INVENTION
  • As noted above, the present invention provides compounds that modulate hERG activity. Such compounds may be used in vitro or in vivo to modulate hERG activity in a variety of contexts. In a first embodiment, the invention provides compounds of Formula I and pharmaceutically acceptable salts thereof, which modulate hERG activity. Compounds of Formula I are represented by the structure, or salt thereof, of formula (I):
  • Figure US20160108025A1-20160421-C00003
  • wherein R1 is selected from: CO2H or tetrazole and R2 is selected from: H, halo, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl, or R1 is H and R2 is CO2H or tetrazole; X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, NR8R9, halo-substituted(C1-C4)alkyl, phenyl or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said phenyl or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl, hydroxy-substituted(C1-C4)alkyl, (C1-C4)alkylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl; R8 is selected from: H, or (C1-C4)alkyl; R9 is selected from: H, or (C1-C4)alkyl;
    • R3 is
  • Figure US20160108025A1-20160421-C00004
  • where R3a is selected from: H, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl; R3b is selected from: H, (C1-C4)alkyl or taken together with R3a forms a 3 to 7 membered saturated cycloalkyl or a 3 to 7 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N; R3c is selected from: H or CH3; R3d is selected from: H or CH3; R4 is selected from:
  • Figure US20160108025A1-20160421-C00005
  • wherein the dotted line indicates the point of attachment; R5 is selected from: H or CH3; R6 is independently selected from: halo, nitrile, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, nitrile-substituted(C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkoxy, nitrile-substituted(C1-C4)alkoxy, (C1-C4)alkylene, N-acetyl, trifluouroacetyl, (C1-C4)alkylthio, halo-substituted thio, halo-substituted (C1-C4)alkylthio, (C3-C6)cycloalkyl, methylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl, halo-substituted(C1-C4) hydroxyalkyl, a 4 to 6 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N, or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said heterocycle or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkyl, halo, hydroxyl, amino or (C1-C4)alkoxy; R7 is selected from: H or halo; n is 1, 2 or 3; m is 0, 1 or 2; or R3c and R4 taken together with the amine to which R3c and R4 are attached forms a fully saturated 4 to 7 membered heterocycle, where 1 to 2 of the ring carbons are each independently optionally replaced with a N or O, and said heterocycle is optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, hydroxy(C1-C4)alkyl, cyclopropyl or oxo or a pharmaceutically acceptable salt thereof.
  • In a second embodiment, the invention is a compound, or salt thereof, according to the first embodiment, wherein R1 is selected from: CO2H, or tetrazole; R2 is selected from: H, halo, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl; X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, NR8R9, halo-substituted(C1-C4)alkyl, phenyl or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said phenyl or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl, hydroxy-substituted(C1-C4)alkyl, (C1-C4)alkylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl; R8 is selected from: H, or (C1-C4)alkyl; R9 is selected from: H, or (C1-C4)alkyl;
    • R3 is
  • Figure US20160108025A1-20160421-C00006
  • where R3a is selected from: H, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl; R3b is selected from: H, (C1-C4)alkyl or taken together with R3a forms a 3 to 7 membered saturated cycloalkyl or a 3 to 7 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N; R3c is selected from: H or CH3; R3d is selected from: H or CH3; R4 is selected from:
  • Figure US20160108025A1-20160421-C00007
  • wherein the dotted line indicates the point of attachment; R5 is selected from: H or CH3; R6 is independently selected from: halo, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkoxy, nitrile-substituted(C1-C4)alkoxy, (C1-C4)alkylene, N-acetyl, trifluouroacetyl, (C1-C4)alkylthio, halo-substituted thio, halo-substituted (C1-C4)alkylthio, (C3-C6)cycloalkyl, methylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl, halo-substituted(C1-C4) hydroxyalkyl, a 4 to 6 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N, or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said heterocycle or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkyl, halo, hydroxyl, amino or (C1-C4)alkoxy; R7 is selected from: H or halo; n is 1, 2 or 3; m is 0, 1 or 2; or R3c and R4 taken together with the amine to which R3c and R4 are attached forms a fully saturated 4 to 7 membered heterocycle, where 1 to 2 of the ring carbons are each independently optionally replaced with a N or O, and said heterocycle is optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, hydroxy(C1-C4)alkyl, cyclopropyl or oxo or a pharmaceutically acceptable salt thereof.
  • In one embodiment, the invention is the compound, or pharmaceutically acceptable salt thereof, according any one of the preceding embodiments, wherein R1 is tetrazole.
  • In another embodiment, the invention is the compound, or pharmaceutically acceptable salt thereof, according any one of the preceding embodiments, wherein R2 is hydrogen.
  • In a third embodiment, the invention is the compound according to the first or secon embodiments, or a salt thereof, wherein the compound is of formula (II):
  • Figure US20160108025A1-20160421-C00008
  • In a fourth embodiment, the invention is the compound according to any one of the first through third embodiments, or a salt thereof, wherein the compound is of formula (III):
  • Figure US20160108025A1-20160421-C00009
  • In a fifth embodiment, the invention is the compound according to any one of the first through third embodiments, or a salt thereof, wherein the compound is of formula (IV):
  • Figure US20160108025A1-20160421-C00010
  • In a sixth embodiment, the invention is the compound according any one of the first through fourth embodiments, or a salt thereof, wherein the compound is of formula (V):
  • Figure US20160108025A1-20160421-C00011
  • In a seventh embodiment, the invention is the compound according to any one of the first through fourth or sixth embodiments, or a salt thereof, wherein the compound is of formula (VI):
  • Figure US20160108025A1-20160421-C00012
  • wherein, R2 is selected from: H, CH3 or CF3; X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl; R6 is independently selected from: halo, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkoxy; or a pharmaceutically acceptable salt thereof
  • In an eighth embodiment, the invention is the compound according to any one of first or second embodiments, or a salt thereof, wherein the compound is of formula (VII):
  • Figure US20160108025A1-20160421-C00013
  • In a ninth embodiment, the invention is the compound according to any one of the first, second or eighth embodiments, or a salt thereof, wherein the compound is of formula (VIII):
  • Figure US20160108025A1-20160421-C00014
  • In a tenth embodiment, the invention is the compound according to any one of the first, second or eighth embodiments, or a salt thereof, wherein the compound is of formula (IX):
  • Figure US20160108025A1-20160421-C00015
  • In an eleventh embodiment, the invention is the compound, or salt thereof, according to any one of the first through tenth embodiments, wherein X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl; R3b is H; or a pharmaceutically acceptable salt thereof.
  • In a twelfth embodiment, the invention is the compound according to the first embodiment, or a salt thereof, wherein the compound is selected from:
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-5-fluoro-4-methoxyaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-ethoxy-5-fluoroaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-dibromo-4-(difluoromethoxy)aniline;
    • 3,5-dichloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxyaniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-((trifluoromethyl)thio)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(prop-1-en-2-yl)-4-(trifluoromethoxy)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
    • 4-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
    • 3,4,5-trichloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(difluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4,5-trichloroaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-4-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-((trifluoromethyl)thio)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(methylthio)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(methylthio)aniline;
    • 2-(4-(((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
    • 1-(4-(((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)phenyl)-2,2,2-trifluoroethanone;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-chloroaniline;
    • 3-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4,5-difluoroaniline;
    • 3-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-bromo-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-propylaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(2,2,2-trifluoroethoxy)aniline;
    • 5-(6-((2-(3,4,5-trichlorophenyl)hydrazinyl)methyl)benzofuran-2-yl)-2H-tetrazole;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-bromo-3-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3,5-dichloro-4-ethoxyaniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-(trifluoromethoxy)aniline;
    • N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
    • 3-bromo-N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(2,2,2-trifluoroethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromoaniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4,5-trimethoxyaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-chloro-3-propylaniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-5-methyl-4-propylaniline;
    • 3-chloro-N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-((trifluoromethyl)thio)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-propylaniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-fluoro-3-(trifluoromethoxy)aniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3,4,5-trichloroaniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-5-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethoxy)aniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-ethyl-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-fluoro-4-propylaniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-methyl-4-propylaniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-propylaniline;
    • 6-(((3,4,5-tribromophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,2-difluorobenzo[d][1,3]dioxol-5-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-(trifluoromethyl)-4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(trifluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(methylthio)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-(methylthio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-morpholinophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(pentafluorothio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-ethyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,4-bis(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-methyl-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(2,2,2-trifluoroacetyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,4-bis(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4,5-difluorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-3-(trifluoromethyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-(2,2,2-trifluoroethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-morpholinophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-fluoro-5-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)-3-(trifluoromethyl)benzofuran-2-carboxylic acid;
    • 6-(((5-(trifluoromethyl)pyridin-2-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2-methylbenzo[d]thiazol-5-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-methoxyphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,5-bis(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-methoxy-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,6-dichloropyridin-4-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3-chloro-4-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3,4-dichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((4-ethyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3-propyl-4-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((4-chloro-3-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • 3,4-dichloro-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)aniline;
    • N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 3-bromo-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
    • 4-(difluoromethoxy)-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-(trifluoromethyl)aniline;
    • 4-bromo-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
    • N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • 3-bromo-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
    • 4-bromo-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
    • 3-chloro-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethyl)aniline;
    • 3,4-dichloro-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)aniline;
    • 3-bromo-N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
    • 4-(difluoromethoxy)-N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-(trifluoromethyl)aniline
    • N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • 4-bromo-N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
    • N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 4-(difluoromethoxy)-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-(trifluoromethyl)aniline;
    • N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • 3-bromo-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
    • 4-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • 4-bromo-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
    • 4-(difluoromethoxy)-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • N-((5-methoxy-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • 2-(4-(((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
    • N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2-difluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
    • 4-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
    • 3-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropylaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
    • 4-ethoxy-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • 4-(2,2-difluoroethoxy)-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 4-(difluoromethoxy)-N-((5-methoxy-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • 4-(difluoromethoxy)-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((5-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-ethoxyaniline;
    • N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-methoxyaniline;
    • N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 4-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
    • 3-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
    • N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
    • 6-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-5-(trifluoromethyl)pyridin-3-amine;
    • 3-bromo-4-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • 3-bromo-4-ethyl-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-chloroaniline;
    • 3-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 3,5-dibromo-4-(difluoromethoxy)-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • 3-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • 7-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2-methylbenzofuran-5-amine;
    • 4-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
    • 3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
    • N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • 3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • 3-bromo-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-7-chloro-2-methylbenzofuran-5-amine;
    • N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-5-(trifluoromethyl)aniline;
    • 3-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
    • 2-(difluoromethoxy)-5-(((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)benzonitrile;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)aniline;
    • 5-(((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(difluoromethoxy)benzonitrile;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-5-(trifluoromethyl)aniline;
    • 5-(((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(difluoromethoxy)benzonitrile;
    • 3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-6-chloro-5-(trifluoromethyl)pyridin-3-amine;
    • 3-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)aniline;
    • N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropyl-3-(trifluoromethyl)aniline;
    • 3,4-dichloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl benzo[d]isothiazol-5-amine;
    • 2-(4-(((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
    • 3-chloro-4-ethoxy-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-5-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-5-(trifluoromethyl)aniline;
    • 4-chloro-3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • 3-chloro-4-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-isobutoxyaniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxyaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2-fluoro-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2,2,4,4-tetrafluoro-4H-benzo[d][1,3]dioxin-6-amine;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-5-methyl-4-propylaniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(2,2,2-trifluoroethyl)aniline;
    • N, N-bis((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-isobutoxyaniline;
    • 7-(((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-4-(trifluoromethyl)-2H-chromen-2-one;
    • 5-chloro-6-(((4-(difluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-chloro-6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-(2,2,2-trifluoroethoxy)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-(trifluoromethoxy)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-((trifluoromethyl)thio)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
    • 6-(((4-bromo-3,5-bis(trifluoromethyl)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
    • 6-(((4-(difluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
    • 5-fluoro-6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-fluoro-6-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid; and
    • N-((3-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline.
  • In another embodiment, the invention is the compound according to the first or twelfth embodiments, or a salt thereof, wherein the compound is selected from:
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-5-fluoro-4-methoxyaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-ethoxy-5-fluoroaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-dibromo-4-(difluoromethoxy)aniline;
    • 3,5-dichloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxyaniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-((trifluoromethyl)thio)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(prop-1-en-2-yl)-4-(trifluoromethoxy)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
    • 4-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
    • 3,4,5-trichloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(difluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4,5-trichloroaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-4-(trifluoromethoxy)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-((trifluoromethyl)thio)aniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(methylthio)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(methylthio)aniline;
    • 2-(4-(((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
    • 1-(4-(((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)phenyl)-2,2,2-trifluoroethanone;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • 3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-chloroaniline;
    • 3-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4,5-difluoroaniline;
    • 3-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-bromo-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-propylaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(2,2,2-trifluoroethoxy)aniline;
    • 5-(6-((2-(3,4,5-trichlorophenyl)hydrazinyl)methyl)benzofuran-2-yl)-2H-tetrazole;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-bromo-3-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3,5-dichloro-4-ethoxyaniline;
    • N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-(trifluoromethoxy)aniline;
    • N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
    • 3-bromo-N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(2,2,2-trifluoroethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromoaniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethyl)aniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4,5-trimethoxyaniline;
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-chloro-3-propylaniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-5-methyl-4-propylaniline;
    • 3-chloro-N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-((trifluoromethyl)thio)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-propylaniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-fluoro-3-(trifluoromethoxy)aniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3,4,5-trichloroaniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-5-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethoxy)aniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-(trifluoromethoxy)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-ethyl-3-(trifluoromethyl)aniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-fluoro-4-propylaniline;
    • N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-methyl-4-propylaniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
    • N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-propylaniline;
    • 6-(((3,4,5-tribromophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,2-difluorobenzo[d][1,3]dioxol-5-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-(trifluoromethyl)-4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(trifluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(methylthio)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-(methylthio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-morpholinophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(pentafluorothio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-ethyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,4-bis(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-methyl-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(2,2,2-trifluoroacetyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,4-bis(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4,5-difluorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-3-(trifluoromethyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-(2,2,2-trifluoroethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-morpholinophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-fluoro-5-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)-3-(trifluoromethyl)benzofuran-2-carboxylic acid;
    • 6-(((5-(trifluoromethyl)pyridin-2-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2-methylbenzo[d]thiazol-5-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3-chloro-4-methoxyphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((3,5-bis(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-methoxy-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 6-(((2,6-dichloropyridin-4-yl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3-chloro-4-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3,4-dichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((4-ethyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
    • 5-(((3-propyl-4-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid; and
    • 5-(((4-chloro-3-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid.
  • In one embodiment, the invention is the compound, or salt thereof: N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline.
  • In another embodiment, the invention is the compound, or salt thereof: N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline.
  • In a thirteenth embodiment, the invention is a pharmaceutical composition comprising a therapeutically effective amount of a compound according to any one of the preceding embodiments, or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable carriers.
  • In a fourteenth embodiment, the invention is a combination comprising a therapeutically effective amount of a compound according to any one of the preceding embodiments or a pharmaceutically acceptable salt thereof and one or more therapeutically active co-agents.
  • In a fifteenth embodiment, the invention is a method to treat, prevent or ameliorate a hERG related condition, comprising administering to a subject in need thereof an effective amount of a compound or pharmaceutically acceptable salt thereof of any one of the preceding embodiments.
  • In a sixteenth embodiment, the invention is the method according to the fifteenth embodiment, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • In one embodiment, the invention is a compound according to any one of the preceding embodiments, or a pharmaceutically acceptable salt thereof, for use as a medicament.
  • In another embodiment, the invention is a compound according to any one of the preceding embodiments, or a pharmaceutically acceptable salt thereof, for use in the treatment of a hERG related condition.
  • In yet another embodiment, the invention is the compound according to the preceding embodiment, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • In another embodiment, the invention is the use of a compound according to any one of the preceding embodiments or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the treatment of a hERG related condition.
  • In yet another embodiment, the invention is the use of a compound according to the preceding embodiment, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • For purposes of interpreting this specification, the following definitions will apply and whenever appropriate, terms used in the singular will also include the plural and vice versa.
  • As used herein, the term “C1-4alkyl” refers to a fully saturated branched or unbranched hydrocarbon moiety having 1 to 4 carbon atoms. The terms “C1-6alkyl” and “C1-10alkyl” are to be construed accordingly. Representative examples of C1-10alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl, 2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl and n-decyl.
  • As used herein, the term “C1-4alkylene” refers to divalent alkyl group as defined herein above having 1 to 4 carbon atoms. The terms “C1-6alkylene” and “C1-10alkylene” are to be construed accordingly. Representative examples of C1-10alkylene include, but are not limited to, methylene, ethylene, n-propylene, iso-propylene, n-butylene, sec-butylene, iso-butylene, tert-butylene, n-pentylene, isopentylene, neopentylene, n-hexylene, 3-methylhexylene, 2,2-dimethylpentylene, 2,3-dimethylpentylene, n-heptylene, n-octylene, n-nonylene and n-decylene.
  • As used herein, the term “halo-substituted(C1-C4)alkyl” refers to a C1-4alkyl group as defined herein, wherein at least one of the hydrogen atoms is replaced by a halo atom. The haloC1-4alkyl group can be monohaloC1-4alkyl, dihaloC1-4alkyl or polyhaloC1-4alkyl including perhaloC1-4alkyl. A monohaloC1-4alkyl can have one iodo, bromo, chloro or fluoro within the alkyl group. DihaloC1-4alkyl and polyhaloC1-4alkyl groups can have two or more of the same halo atoms or a combination of different halo groups within the alkyl. Typically the polyhaloC1-4alkyl group contains up to 12, or 10, or 8, or 6, or 4, or 3, or 2 halo groups. Non-limiting examples of haloC1-4alkyl include fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl, difluoroethyl, difluoropropyl, dichloroethyl and dichloropropyl. A perhaloC1-4alkyl group refers to a C1-4alkyl group having all hydrogen atoms replaced with halo atoms.
  • As used herein, the term “C1-4alkylthio” refers to C1-4alkyl-S—, wherein C1-4alkyl is defined herein above. The terms “C1-6alkylthio” and “C1-10alkylthio” are to be construed accordingly. Representative examples of C1-4alkylthio include, but are not limited to, methylthio, ethylthio, n-propylthio, iso-propylthio, n-butylthio, sec-butylthio, iso-butylthio and tert-butylthio.
  • As used herein, the term “haloC1-4alkylthio” refers to a C1-4alkylthio group as defined herein, wherein at least one of the hydrogen atoms is replaced by a halo atom. The haloC1-4alkylthio group can be monohaloC1-4alkylthio, dihaloC1-4alkylthio or polyhaloC1-4alkylthio including perhaloC1-4alkylthio. A monohaloC1-4alkylthio can have one iodo, bromo, chloro or fluoro within the alkylthio group. DihaloC1-4alkylthio and polyhaloC1-4alkylthio groups can have two or more of the same halo atoms or a combination of different halo groups within the alkylthio. Typically the polyhaloC1-4alkylthio group contains up to 8, or 6, or 4, or 3, or 2 halo groups. Non-limiting examples of haloC1-10alkylthio include fluoromethylthio, difluoromethylthio, trifluoromethylthio, chloromethylthio, dichloromethylthio, trichloromethylthio, pentafluoroethylthio, heptafluoropropylthio, difluorochloromethylthio, dichlorofluoromethylthio, difluoroethylthio, difluoropropylthio, dichloroethylthio and dichloropropylthio. A perhaloC1-4alkylthio group refers to a C1-10alkylthio group having all hydrogen atoms replaced with halo atoms.
  • The term “aryl” refers to an aromatic hydrocarbon group having 6-20 carbon atoms in the ring portion. Typically, aryl is monocyclic, bicyclic or tricyclic aryl having 6-20 carbon atoms and includes one or more aromatic rings fused to one or more non-aromatic hydrocarbon rings. Non-limiting examples include phenyl, naphthyl or tetrahydronaphthyl.
  • As used herein, the term “C1-4alkoxy” or “C1-4alkoxyl” refers to C1-4alkyl-O—, wherein C1-4alkyl is defined herein above. Representative examples of C1-4alkoxy include, but are not limited to, methoxy, ethoxy, propoxy, 2-propoxy, butoxy and tert-butoxy.
  • As used herein, the term “halo-substituted(C1-C4)alkoxy” refers to a C1-4alkoxy group as defined herein, wherein at least one of the hydrogen atoms is replaced by a halo atom. The haloC1-4alkoxy group can be monohaloC1-4alkoxy, dihaloC1-4alkoxy or polyhaloC1-4alkoxy including perhaloC1-4alkoxy. A monohaloC1-4alkoxy can have one iodo, bromo, chloro or fluoro within the alkoxy group. DihaloC1-4alkoxy and polyhaloC1-4alkoxy groups can have two or more of the same halo atoms or a combination of different halo groups within the alkoxy. Typically the polyhaloC1-4alkoxy group contains up to 8, or 6, or 4, or 3, or 2 halo groups. Non-limiting examples of haloC1-4alkyl include fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy, trichloromethoxy, pentafluoroethoxy, heptafluoropropoxy, difluorochloromethoxy, dichlorofluoromethoxy, difluoroethoxy, difluoropropoxy, dichloroethoxy and dichloropropoxy. A perhaloC1-4alkoxy group refers to a C1-4alkoxy group having all hydrogen atoms replaced with halo atoms.
  • As used herein, the term “heterocyclyl” or “heterocyclo” refers to a saturated or unsaturated non-aromatic ring or ring system, which is a 4-, 5-, 6-, or 7-membered monocyclic ring containing 1, 2 or 3 heteroatoms selected from O, S and N, a 7-, 8-, 9-, 10-, 11-, or 12-membered bicyclic ring system containing 1, 2, 3, 4 or 5 heteroatoms selected from O, S and N, or a 10-, 11-, 12-, 13-, 14- or 15-membered tricyclic ring system and containing 1, 2, 3, 4, 5, 6 or 7 heteroatoms selected from O, S and N, where the N and S can also optionally be oxidized to various oxidation states. The heterocyclic group can be attached via a heteroatom or a carbon atom. The heterocyclyl can include fused or bridged rings as well as spirocyclic rings. Examples of heterocycles include tetrahydrofuran (THF), dihydrofuran, 1,4-dioxane, morpholine, 1,4-dithiane, piperazine, piperidine, 1,3-dioxolane, imidazolidine, imidazoline, pyrroline, pyrrolidine, tetrahydropyran, dihydropyran, oxathiolane, dithiolane, 1,3-dioxane, 1,3-dithiane, oxathiane and thiomorpholine.
  • As used herein, the term “C3-6cycloalkyl” refers to saturated or unsaturated monocyclic, bicyclic or tricyclic hydrocarbon groups of 3-6 carbon atoms. The term “C3-6cycloalkyl” refers to a fully saturated or unsaturated monocyclic hydrocarbon group of 3-8 carbon atoms. Exemplary monocyclic hydrocarbon groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl and cyclohexenyl.
  • As used herein, the term “heteroaryl” refers to a 5-, 6-, or 7-membered monocyclic aromatic ring containing 1, 2, 3 or 4 heteroatoms selected from O, S and N, an 8-, 9-, or 10-membered fused bicyclic ring system containing 1, 2, 3, 4 or 5 heteroatoms selected from O, S and N, or an 11-, 12-, 13-, or 14-membered fused tricyclic ring system containing 1, 2, 3, 4, 5 or 6 heteroatoms selected from O, S and N, wherein at least one of the rings of the bicyclic or tricyclic ring systems is fully aromatic. Typical heteroaryl groups include 2- or 3-thienyl, 2- or 3-furyl, 2- or 3-pyrrolyl, 2-, 4-, or 5-imidazolyl, 3-, 4-, or 5-pyrazolyl, 2-, 4-, or 5-thiazolyl, 3-, 4-, or 5-isothiazolyl, 2-, 4-, or 5-oxazolyl, 3-, 4-, or 5-isoxazolyl, 3- or 5-1,2,4-triazolyl, 4- or 5-1,2,3-triazolyl, tetrazolyl, 2-, 3-, or 4-pyridyl, 3- or 4-pyridazinyl, 3-, 4-, or 5-pyrazinyl, 2-pyrazinyl, 2-, 4-, or 5-pyrimidinyl, 1-, 2-, 3-, 5-, 6-, 7-, or 8-indolizinyl, 1-, 3-, 4-, 5-, 6-, or 7-isoindolyl, 2-, 3-, 4-, 5-, 6-, or 7-indolyl, 2-, 3-, 4-, 5-, 6-, or 7-indazolyl, 2-, 4-, 5-, 6-, 7-, or 8-purinyl, 1-, 2-, 3-, 4-, 6-, 7-, 8-, or 9-quinolizinyl, 2-, 3-, 4-, 5-, 6-, 7-, or 8-quinoliyl, 1-, 3-, 4-, 5-, 6-, 7-, or 8-isoquinolinyl, 1-, 4-, 5-, 6-, 7-, or 8-phthalazinyl, 2-, 3-, 4-, 5- , or 6-naphthyridinyl, 2-, 3-, 5-, 6-, 7-, or 8-quinazolinyl, 3-, 4-, 5-, 6-, 7-, or 8-cinnolinyl, 2-, 4-, 6-, or 7-pteridinyl, 1-, 2-, 3-, 4-, 5-, 6-, 7-, or 8-4aH carbazolyl, 1-, 2-, 3-, 4-, 5-, 6-, 7-, or 8-carbzaolyl, 1-, 3-, 4-, 5-, 6-, 7-, 8-, or 9-carbolinyl, 1-, 2-, 3-, 4-, 6-, 7-, 8-, 9-, or 10-phenanthridinyl, 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, or 9-acridinyl, 1-, 2-, 4-, 5-, 6-, 7-, 8-, or 9-perimidinyl, 2-, 3-, 4-, 5-, 6-, 8-, 9-, or 10-phenathrolinyl, 1-, 2-, 3-, 4-, 6-, 7-, 8-, or 9-phenazinyl, 1-, 2-, 3-, 4-, 6-, 7-, 8-, 9-, or 10-phenothiazinyl, 1-, 2-, 3-, 4-, 6-, 7-, 8-, 9-, or 10-phenoxazinyl, 2-, 3-, 4-, 5-, 6-, or 1-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, or 10-benzisoqinolinyl, 2-, 3-, 4-, or thieno[2,3-b]furanyl, 2-, 3-, 5-, 6-, 7-, 8-, 9-, 10-, or 11-7H-pyrazino[2,3-c]carbazolyl, 2-, 3-, 5-, 6-, or 7-2H-furo[3,2-b]-pyranyl, 2-, 3-, 4-, 5-, 7-, or 8-5H-pyrido[2,3-d]-o-oxazinyl, 1-, 3-, or 5-1H-pyrazolo[4,3-d]-oxazolyl, 2-, 4-, or 54H-imidazo[4,5-d]thiazolyl, 3-, 5-, or 8-pyrazino[2,3-d]pyridazinyl, 2-, 3-, 5-, or 6-imidazo[2,1-b]thiazolyl, 1-, 3-, 6-, 7-, 8-, or 9-furo[3,4-c]cinnolinyl, 1-, 2-, 3-, 4-, 5-, 6-, 8-, 9-, 10, or 11-4H-pyrido[2,3-c]carbazolyl, 2-, 3-, 6-, or 7-imidazo[1,2-b][1,2,4]triazinyl, 7-benzo[b]thienyl, 2-, 4-, 5-, 6-, or 7-benzoxazolyl, 2-, 4-, 5-, 6-, or 7-benzimidazolyl, 2-, 4-, 4-, 5-, 6-, or 7-benzothiazolyl, 1-, 2-, 4-, 5-, 6-, 7-, 8-, or 9-benzoxapinyl, 2-, 4-, 5-, 6-, 7-, or 8-benzoxazinyl, 1-, 2-, 3-, 5-, 6-, 7-, 8-, 9-, 10-, or 11-1H-pyrrolo[1,2-b][2]benzazapinyl, 2-, 3-, 4-, 5-, 6-, 7-, or 8-quinolinyl, 1-, 3-, 4-, 5-, 6-, 7-, or 8-isoquinolinyl, 2-, 3-, 4-, 5-, 6-, or 7-indolyl, 2-, 3-, 4-, 5-, 6-, or 7-benzo[b]thienyl, 2-, 4-, 5-, 6-, or 7-benzoxazolyl, 2-, 4-, 5-, 6-, or 7-benzimidazolyl, 2-, 4-, 5-, 6-, or 7-benzothiazolyl and tetrazole.
  • As used herein, the term “tetrazole” refers to both 1-tetrazole and 2-tetrazole, i.e.
  • Figure US20160108025A1-20160421-C00016
  • As used herein, the term “halogen” or “halo” refers to fluoro, chloro, bromo, and iodo.
  • As used herein, the term “isomers” refers to different compounds that have the same molecular formula but differ in arrangement and configuration of the atoms, e.g. 1-tetrazole and 2-tetrazole are inseparable isomers. Also as used herein, the term “an optical isomer” or “a stereoisomer” refers to any of the various stereo isomeric configurations which may exist for a given compound of the present invention and includes geometric isomers. It is understood that a substituent may be attached at a chiral center of a carbon atom. Therefore, the invention includes enantiomers, diastereomers or racemates of the compound. “Enantiomers” are a pair of stereoisomers that are non-superimposable mirror images of each other. A 1:1 mixture of a pair of enantiomers is a “racemic” mixture. The term is used to designate a racemic mixture where appropriate. “Diastereoisomers” are stereoisomers that have at least two asymmetric atoms, but which are not mirror-images of each other. The absolute stereochemistry is specified according to the Cahn-Ingold-Prelog R-S system. When a compound is a pure enantiomer the stereochemistry at each chiral carbon may be specified by either R or S. Resolved compounds whose absolute configuration is unknown can be designated (+) or (−) depending on the direction (dextro- or levorotatory) which they rotate plane polarized light at the wavelength of the sodium D line. Certain of the compounds described herein contain one or more asymmetric centers or axes and may thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)-. The present invention is meant to include all such possible isomers, including racemic mixtures, optically pure forms and intermediate mixtures. Optically active (R)- and (S)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques. If the compound contains a double bond, the substituent may be E or Z configuration. If the compound contains a disubstituted cycloalkyl, the cycloalkyl substituent may have a cis- or trans-configuration. All tautomeric forms are also intended to be included.
  • As used herein, the terms “salt” or “salts” refers to an acid addition or base addition salt of a compound of the invention. “Salts” include in particular “pharmaceutical acceptable salts.” The term “pharmaceutically acceptable salts” refers to salts that retain the biological effectiveness and properties of the compounds of this invention and, which typically are not biologically or otherwise undesirable. In many cases, the compounds of the present invention are capable of forming acid and/or base salts by virtue of the presence of amino and/or carboxyl groups or groups similar thereto.
  • Pharmaceutically acceptable acid addition salts can be formed with inorganic acids and organic acids, e.g., acetate, aspartate, benzoate, besylate, bromide/hydrobromide, bicarbonate/carbonate, bisulfate/sulfate, camphorsulfornate, chloride/hydrochloride, chlortheophyllonate, citrate, ethandisulfonate, fumarate, gluceptate, gluconate, glucuronate, hippurate, hydroiodide/iodide, isethionate, lactate, lactobionate, laurylsulfate, malate, maleate, malonate, mandelate, mesylate, methylsulphate, naphthoate, napsylate, nicotinate, nitrate, octadecanoate, oleate, oxalate, palmitate, pamoate, phosphate/hydrogen phosphate/di hydrogen phosphate, polygalacturonate, propionate, stearate, succinate, sulfosalicylate, tartrate, tosylate and trifluoroacetate salts.
  • Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like.
  • Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, sulfosalicylic acid, and the like. Pharmaceutically acceptable base addition salts can be formed with inorganic and organic bases.
  • Inorganic bases from which salts can be derived include, for example, ammonium salts and metals from columns I to XII of the periodic table. In certain embodiments, the salts are derived from sodium, potassium, ammonium, calcium, magnesium, iron, silver, zinc, and copper; particularly suitable salts include ammonium, potassium, sodium, calcium and magnesium salts.
  • Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines, basic ion exchange resins, and the like. Certain organic amines include isopropylamine, benzathine, cholinate, diethanolamine, diethylamine, lysine, meglumine, piperazine and tromethamine.
  • The pharmaceutically acceptable salts of the present invention can be synthesized from a parent compound, a basic or acidic moiety, by conventional chemical methods. Generally, such salts can be prepared by reacting free acid forms of these compounds with a stoichiometric amount of the appropriate base (such as Na, Ca, Mg, or K hydroxide, carbonate, bicarbonate or the like), or by reacting free base forms of these compounds with a stoichiometric amount of the appropriate acid. Such reactions are typically carried out in water or in an organic solvent, or in a mixture of the two. Generally, use of non-aqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile is desirable, where practicable. Lists of additional suitable salts can be found, e.g., in “Remington's Pharmaceutical Sciences”, 20th ed., Mack Publishing Company, Easton, Pa., (1985); and in “Handbook of Pharmaceutical Salts: Properties, Selection, and Use” by Stahl and Wermuth (Wiley-VCH, Weinheim, Germany, 2002).
  • Any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds. Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, and chlorine, such as 2H, 3H, 11C, 13C, 14C, 15N, 18F 31P, 32P, 35S, 36Cl, 125I respectively. The invention includes various isotopically labeled compounds as defined herein, for example those into which radioactive isotopes, such as 3H, 13C, and 14C, are present. Such isotopically labelled compounds are useful in metabolic studies (with 14C), reaction kinetic studies (with, for example 2H or 3H), detection or imaging techniques, such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT) including drug or substrate tissue distribution assays, or in radioactive treatment of patients. In particular, an 18F or labeled compound may be particularly desirable for PET or SPECT studies. Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.
  • Further, substitution with heavier isotopes, particularly deuterium (i.e., 2H or D) may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements or an improvement in therapeutic index. It is understood that deuterium in this context is regarded as a substituent of a compound of the formula (I). The concentration of such a heavier isotope, specifically deuterium, may be defined by the isotopic enrichment factor. The term “isotopic enrichment factor” as used herein means the ratio between the isotopic abundance and the natural abundance of a specified isotope. If a substituent in a compound of this invention is denoted deuterium, such compound has an isotopic enrichment factor for each designated deuterium atom of at least 3500 (52.5% deuterium incorporation at each designated deuterium atom), at least 4000 (60% deuterium incorporation), at least 4500 (67.5% deuterium incorporation), at least 5000 (75% deuterium incorporation), at least 5500 (82.5% deuterium incorporation), at least 6000 (90% deuterium incorporation), at least 6333.3 (95% deuterium incorporation), at least 6466.7 (97% deuterium incorporation), at least 6600 (99% deuterium incorporation), or at least 6633.3 (99.5% deuterium incorporation).
  • Isotopically-labeled compounds of formula (I) can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying Examples and Preparations using an appropriate isotopically-labeled reagents in place of the non-labeled reagent previously employed.
  • Pharmaceutically acceptable solvates in accordance with the invention include those wherein the solvent of crystallization may be isotopically substituted, e.g., D2O, d6-acetone, d6-DMSO.
  • Compounds of the invention, i.e. compounds of formula (I) that contain groups capable of acting as donors and/or acceptors for hydrogen bonds may be capable of forming co-crystals with suitable co-crystal formers. These co-crystals may be prepared from compounds of formula (I) by known co-crystal forming procedures. Such procedures include grinding, heating, co-subliming, co-melting, or contacting in solution compounds of formula (I) with the co-crystal former under crystallization conditions and isolating co-crystals thereby formed. Suitable co-crystal formers include those described in WO 2004/078163. Hence the invention further provides co-crystals comprising a compound of formula (I).
  • The term “a therapeutically effective amount” of a compound of the present invention refers to an amount of the compound of the present invention that will elicit the biological or medical response of a subject, for example, reduction or inhibition of an enzyme or a protein activity, or ameliorate symptoms, alleviate conditions, slow or delay disease progression, or prevent a disease, etc. In one non-limiting embodiment, the term “a therapeutically effective amount” refers to the amount of the compound of the present invention that, when administered to a subject, is effective to (1) at least partially alleviate, inhibit, prevent and/or ameliorate a condition, or a disorder or a disease mediated by hERG; or (2) activating the activity of hERG.
  • In another non-limiting embodiment, the term “a therapeutically effective amount” refers to the amount of the compound of the present invention that, when administered to a cell, or a tissue, or a non-cellular biological material, or a medium, is effective to at least partially activating the activity of hERG; or at least partially activating the expression of hERG.
  • The phrases “therapeutically effective amount” and “effective amount” are used herein to mean an amount sufficient to reduce by at least about 15 percent, preferably by at least 50 percent, more preferably by at least 90 percent, and most preferably prevent, a clinically significant deficit in the activity, function and response of the host. Alternatively, a therapeutically effective amount is sufficient to cause an improvement in a clinically significant condition/symptom in the host.
  • The effective amount can vary depending on such factors as the size and weight of the subject, the type of illness, or the particular compound of the invention. For example, the choice of the compound of the invention can affect what constitutes an “effective amount.” One of ordinary skill in the art would be able to study the factors contained herein and make the determination regarding the effective amount of the compounds of the invention without undue experimentation.
  • The regimen of administration can affect what constitutes an effective amount. The compound of the invention can be administered to the subject either prior to or after the onset of a hERG related condition. Further, several divided dosages, as well as staggered dosages, can be administered daily or sequentially, or the dose can be continuously infused, or can be a bolus injection. Further, the dosages of the compound(s) of the invention can be proportionally increased or decreased as indicated by the exigencies of the therapeutic or prophylactic situation.
  • As used herein, the term “subject” refers to an animal. Typically the animal is a mammal. A subject also refers to for example, primates (e.g., humans, male or female), cows, sheep, goats, horses, dogs, cats, rabbits, rats, mice, fish, birds and the like. In certain embodiments, the subject is a primate. In yet other embodiments, the subject is a human.
  • As used herein, the term “inhibit”, “inhibition” or “inhibiting” refers to the reduction or suppression of a given condition, symptom, or disorder, or disease, or a significant decrease in the baseline activity of a biological activity or process.
  • As used herein, the term “treat”, “treating” or “treatment” of any disease or disorder refers in one embodiment, to ameliorating the disease or disorder (i.e., slowing or arresting or reducing the development of the disease or at least one of the clinical symptoms thereof). In another embodiment “treat,” “treating,” or “treatment” refers to alleviating or ameliorating at least one physical parameter including those which may not be discernible by the patient. In yet another embodiment, “treat”, “treating” or “treatment” refers to modulating the disease or disorder, either physically (e.g., through stabilization of a discernible symptom), physiologically, (e.g., through stabilization of a physical parameter), or both. In yet another embodiment, “treat,” “treating,” or “treatment” refers to preventing or delaying the onset or development or progression of the disease or disorder.
  • As used herein, a subject is “in need of” a treatment if such subject would benefit biologically, medically or in quality of life from such treatment.
  • As used herein, the term “a,” “an,” “the” and similar terms used in the context of the present invention (especially in the context of the claims) are to be construed to cover both the singular and plural unless otherwise indicated herein or clearly contradicted by the context.
  • All methods described herein can be performed in any suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of any and all examples, or exemplary language (e.g., “such as”) provided herein is intended merely to better illuminate the invention and does not pose a limitation on the scope of the invention otherwise claimed.
  • Any asymmetric atom (e.g., carbon or the like) of the compound(s) of the present invention can be present in racemic or enantiomerically enriched, for example the (R)-, (S)- or (R,S)-configuration. In certain embodiments, each asymmetric atom has at least 50% enantiomeric excess, at least 60% enantiomeric excess, at least 70% enantiomeric excess, at least 80% enantiomeric excess, at least 90% enantiomeric excess, at least 95% enantiomeric excess, or at least 99% enantiomeric excess in the (R)- or (S)-configuration. Substituents at atoms with unsaturated bonds may, if possible, be present in cis-(Z)- or trans-(E)-form.
  • Accordingly, as used herein a compound of the present invention can be in the form of one of the possible isomers, rotamers, atropisomers, tautomers or mixtures thereof, for example, as substantially pure geometric (cis or trans) isomers, diastereomers, optical isomers (antipodes), racemates or mixtures thereof.
  • Any resulting mixtures of isomers can be separated on the basis of the physicochemical differences of the constituents, into the pure or substantially pure geometric or optical isomers, diastereomers, racemates, for example, by chromatography and/or fractional crystallization.
  • Any resulting racemates of final products or intermediates can be resolved into the optical antipodes by known methods, e.g., by separation of the diastereomeric salts thereof, obtained with an optically active acid or base, and liberating the optically active acidic or basic compound. In particular, a basic moiety may thus be employed to resolve the compounds of the present invention into their optical antipodes, e.g., by fractional crystallization of a salt formed with an optically active acid, e.g., tartaric acid, dibenzoyl tartaric acid, diacetyl tartaric acid, di-O,O′-p-toluoyl tartaric acid, mandelic acid, malic acid or camphor-10-sulfonic acid. Racemic products can also be resolved by chiral chromatography, e.g., high pressure liquid chromatography (HPLC) using a chiral adsorbent.
  • Compounds of the present invention are either obtained in the free form, as a salt thereof, or as prodrug derivatives thereof.
  • When both a basic group and an acid group are present in the same molecule, the compounds of the present invention may also form internal salts, e.g., zwitterionic molecules.
  • Furthermore, the compounds of the present invention, including their salts, can also be obtained in the form of their hydrates, or include other solvents used for their crystallization. The compounds of the present invention may inherently or by design form solvates with pharmaceutically acceptable solvents (including water); therefore, it is intended that the invention embrace both solvated and unsolvated forms. The term “solvate” refers to a molecular complex of a compound of the present invention (including pharmaceutically acceptable salts thereof) with one or more solvent molecules. Such solvent molecules are those commonly used in the pharmaceutical art, which are known to be innocuous to the recipient, e.g., water, ethanol, and the like. The term “hydrate” refers to the complex where the solvent molecule is water.
  • The compounds of the present invention, including salts, hydrates and solvates thereof, may inherently or by design form polymorphs.
  • The invention further includes any variant of the present processes, in which an intermediate product obtainable at any stage thereof is used as starting material and the remaining steps are carried out, or in which the starting materials are formed in situ under the reaction conditions, or in which the reaction components are used in the form of their salts or optically pure material.
  • Compounds of the invention and intermediates can also be converted into each other according to methods generally known to those skilled in the art.
  • In another aspect, the present invention provides a pharmaceutical composition comprising a compound of the present invention, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. The pharmaceutical composition can be formulated for particular routes of administration such as oral administration, parenteral administration, and rectal administration, etc. In addition, the pharmaceutical compositions of the present invention can be made up in a solid form (including without limitation capsules, tablets, pills, granules, powders or suppositories), or in a liquid form (including without limitation solutions, suspensions or emulsions).
  • The pharmaceutical compositions can be subjected to conventional pharmaceutical operations such as sterilization and/or can contain conventional inert diluents, lubricating agents, or buffering agents, as well as adjuvants, such as preservatives, stabilizers, wetting agents, emulsifers and buffers, etc.
  • Typically, the pharmaceutical compositions are tablets or gelatin capsules comprising the active ingredient together with
  • diluents, e.g., lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and/or glycine;
  • lubricants, e.g., silica, talcum, stearic acid, its magnesium or calcium salt and/or polyethyleneglycol; for tablets also
  • binders, e.g., magnesium aluminum silicate, starch paste, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone; if desired
  • disintegrants, e.g., starches, agar, alginic acid or its sodium salt, or effervescent mixtures; and/or
  • absorbents, colorants, flavors and sweeteners.
  • Tablets may be either film coated or enteric coated according to methods known in the art.
  • Suitable compositions for oral administration include an effective amount of a compound of the invention in the form of tablets, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsion, hard or soft capsules, or syrups or elixirs. Compositions intended for oral use are prepared according to any method known in the art for the manufacture of pharmaceutical compositions and such compositions can contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide pharmaceutically elegant and palatable preparations. Tablets may contain the active ingredient in admixture with nontoxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets. These excipients are, for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid; binding agents, for example, starch, gelatin or acacia; and lubricating agents, for example magnesium stearate, stearic acid or talc. The tablets are uncoated or coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glyceryl distearate can be employed. Formulations for oral use can be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example, peanut oil, liquid paraffin or olive oil.
  • Certain injectable compositions are aqueous isotonic solutions or suspensions, and suppositories are advantageously prepared from fatty emulsions or suspensions. Said compositions may be sterilized and/or contain adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure and/or buffers. In addition, they may also contain other therapeutically valuable substances. Said compositions are prepared according to conventional mixing, granulating or coating methods, respectively, and contain about 0.1-75%, or contain about 1-50%, of the active ingredient.
  • Anhydrous pharmaceutical compositions and dosage forms of the invention can be prepared using anhydrous or low moisture containing ingredients and low moisture or low humidity conditions. An anhydrous pharmaceutical composition may be prepared and stored such that its anhydrous nature is maintained. Accordingly, anhydrous compositions are packaged using materials known to prevent exposure to water such that they can be included in suitable formulary kits. Examples of suitable packaging include, but are not limited to, hermetically sealed foils, plastics, unit dose containers (e.g., vials), blister packs, and strip packs.
  • The invention further provides pharmaceutical compositions and dosage forms that comprise one or more agents that reduce the rate by which the compound of the present invention as an active ingredient will decompose. Such agents, which are referred to herein as “stabilizers,” include, but are not limited to, antioxidants such as ascorbic acid, pH buffers, or salt buffers, etc.
  • The compounds of formula I in free form or in salt form, exhibit valuable pharmacological properties, e.g., as indicated in in vitro tests as provided in the next sections, and are therefore indicated for therapy or for use as research chemicals, e.g., as tool compounds.
  • Thus, as a further embodiment, the present invention provides the use of a compound of formula (I) or a salt thereof in therapy. In a further embodiment, the therapy is selected from a disease which may be treated by modulating hERG protein production. In another embodiment, the disease is selected from the afore-mentioned list, e.g., LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • In another embodiment, the invention provides a method of treating a disease which is treated by modulating hERG protein production comprising administration of a therapeutically acceptable amount of a compound of formula (I) or salt thereof to a patient in need of such therapy. In a further embodiment, the disease is selected from the afore-mentioned list, suitably LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • Thus, as a further embodiment, the present invention provides the use of a compound of formula (I) or salt thereof for the manufacture of a medicament. In a further embodiment, the medicament is for treatment of a disease which may be treated by modulation of hERG protein production. In another embodiment, the disease is selected from the afore-mentioned list, suitably LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
  • The pharmaceutical composition or combination of the present invention can be in unit dosage of about 1-1000 mg of active ingredient(s) for a subject of about 50-70 kg, or about 1-500 mg or about 1-250 mg or about 1-150 mg or about 0.5-100 mg, or about 1-50 mg of active ingredients. The therapeutically effective dosage of a compound, the pharmaceutical composition, or the combinations thereof, is dependent on the species of the subject, the body weight, age and individual condition, the disorder or disease or the severity thereof being treated. A physician, clinician or veterinarian of ordinary skill can readily determine the effective amount of each of the active ingredients necessary to prevent, treat or inhibit the progress of the disorder or disease.
  • The above-cited dosage properties are demonstrable in vitro and in vivo tests using advantageously mammals, e.g., mice, rats, dogs, monkeys or isolated organs, tissues and preparations thereof. The compounds of the present invention can be applied in vitro in the form of solutions, e.g., aqueous solutions, and in vivo either enterally, parenterally, advantageously intravenously, e.g., as a suspension or in aqueous solution. The dosage in vitro may range between about 10−3 molar and 10−9 molar concentrations. A therapeutically effective amount in vivo may range depending on the route of administration, between about 0.1-500 mg/kg, or between about 1-100 mg/kg.
  • The compound of the present invention may be administered either simultaneously with, or before or after, one or more other therapeutic agent. The compound of the present invention may be administered separately, by the same or different route of administration, or together in the same pharmaceutical composition as the other agents.
  • In one embodiment, the invention provides a product comprising a compound of formula (I) and at least one other therapeutic agent as a combined preparation for simultaneous, separate or sequential use in therapy. In one embodiment, the therapy is the treatment of a spinal muscular atrophy. Products provided as a combined preparation include a composition comprising the compound of formula (I) and the other therapeutic agent(s) together in the same pharmaceutical composition, or the compound of formula (I) and the other therapeutic agent(s) in separate form, e.g., in the form of a kit.
  • In one embodiment, the invention provides a pharmaceutical composition comprising a compound of formula (I) and another therapeutic agent(s). Optionally, the pharmaceutical composition may comprise a pharmaceutically acceptable carrier, as described above.
  • In one embodiment, the invention provides a kit comprising two or more separate pharmaceutical compositions, at least one of which contains a compound of formula (I). In one embodiment, the kit comprises means for separately retaining said compositions, such as a container, divided bottle, or divided foil packet. An example of such a kit is a blister pack, as typically used for the packaging of tablets, capsules and the like.
  • The kit of the invention may be used for administering different dosage forms, for example, oral and parenteral, for administering the separate compositions at different dosage intervals, or for titrating the separate compositions against one another. To assist compliance, the kit of the invention typically comprises directions for administration.
  • In the combination therapies of the invention, the compound of the invention and the other therapeutic agent may be manufactured and/or formulated by the same or different manufacturers. Moreover, the compound of the invention and the other therapeutic may be brought together into a combination therapy: (i) prior to release of the combination product to physicians (e.g., in the case of a kit comprising the compound of the invention and the other therapeutic agent); (ii) by the physician themselves (or under the guidance of the physician) shortly before administration; (iii) in the patient themselves, e.g., during sequential administration of the compound of the invention and the other therapeutic agent.
  • The following examples are intended to illustrate the invention and are not to be construed as being limitations thereon. Temperatures are given in degrees Celsius. If not mentioned otherwise, all evaporations are performed under reduced pressure, typically between about 15 mm Hg and 100 mm Hg (=20-133 mbar). The structure of final products, intermediates and starting materials is confirmed by standard analytical methods, e.g., microanalysis and spectroscopic characteristics, e.g., MS, IR, NMR. Abbreviations used are those conventional in the art.
  • All starting materials, building blocks, reagents, acids, bases, dehydrating agents, solvents, and catalysts utilized to synthesis the compounds of the present invention are either commercially available or can be produced by organic synthesis methods known to one of ordinary skill in the art (Houben-Weyl 4th Ed. 1952, Methods of Organic Synthesis, Thieme, Volume 21). Further, the compounds of the present invention can be produced by organic synthesis methods known to one of ordinary skill in the art as shown in the following examples.
    • Preparations of Compounds Intermediates and Examples
  • The following Examples are intended to be illustrative only and not limiting in any way. Unless otherwise noted, the following Intermediates and Examples were purified via silica gel column chromatography using RediSep® Rf columns from Teledyne Isco, Inc. Abbreviations used are those conventional in the art or the following:
  • AcOH acetic acid
    AIBN azobisisobutyronitrile
    AlCl3 aluminium chloride
    Aq aqueous
    Ar aryl
    atm atmosphere
    BOC tert-Butyl-carbonate
    BP boiling point
    Br bromine
    br.s., bs broad singlet
    • ° C. Celsius
  • CaCl2 calcium chloride
    CC column chromatography
    CD2Cl2 deuterated dichloromethane
    CDCl3 deuterated chloroform
    CH2Cl2, DCM dichloromethane
    CH3CN, MeCN acetonitrile
    CO carbon monoxide
    Cs2CO3 caesium carbonate
    CuI copper(I) Iodide
    d doublet
    DCE 1,2-dichloroethene
    dd doublet of doublets
    ddd doublet of doublets of doublets
    • DIPEA N-ethyldiisopropylamine
  • DME 1,4-dimethoxyethane
    • DMF N,N-dimethylformamide
  • DMAP dimethyl aminopyridine
    DMSO dimethylsulfoxide
    DPPF bis(diphenylphosphino)ferrocene
    dq doublet of quartets
    dt doublet of triplets
    EDC 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide
    EtOAc ethyl acetate
    EtOH ethanol
    FCC flash column chromatography
    g gram
    h, hr hour
    HCl hydrochloric acid
    HMPA hexamethylphosphoramide
    H2O water
    HPLC high pressure liquid chromatography
    HT high throughput
    • Hz Hertz
  • IBX 2-lodoxybenzoic acid
    i-PrOH isopropyl alcohol
    H2O water
    K kelvin
    K2CO3 potassium carbonate
    K4Fe(CN)6 potassium ferrocyanide
    KOH potassium hydroxide
    LC liquid chromatography
    LCMS liquid chromatography mass spectroscopy
    LiOH lithium hydroxide
    M molar
    m meta
    m multiplet
    MeOH methanol
    MgSO4 magnesium sulfate
    mg milligram
    MHz mega herz
    mL milliliter
    mm millimeter
    mmol millimole
    min. minute
    MS mass spectroscopy
    mw microwave
    N normal
    N2 nitrogen
    NaBH4 sodium borohydride
    NaH sodium hydride
    NaHMDS sodium hexamethyldisilazane
    NaOEt sodium ethoxide
    NaOH sodium hydroxide
    Na2CO3 sodium carbonate
    NaHCO3 sodium bicarbonate
    Na2SO4 sodium sulfate
    Na2S2O3 sodium thiosulfate
    • NBS N-Bromosuccinimide
  • NEt3, TEA triethylamine
    ng nanogram
    NH3 ammonia
    NMR nuclear magnetic resonance
    quint. quintuplet
    Pd/C palladium on carbon
    PdCl2(PPh3)2 bis(triphenylphosphine)palladium(II) dichloride
    Pd(OAc)2 palladium acetate
    PPh3 triphenylphosphine
    PPT precipitate
    q quartet
    Rf retardation factor
    rt, RT room temperature
    Rt Retention time
    rxn reaction
    s singlet
    sat. saturated
    SM starting material
    SOCl2 thionyl chloride
    sxt sextet
    t triplet
    TFA trifluoroacetic acid
    TFAA trifluoroacetic anhydride
    TFE 2,2,2-trifluoroethanol
    TH F tetrahydrofuran
    Ti(OiPr)4 titanium(IV) isopropoxide
    TLC thin layer chromatography
    TMS-CHN2 trimethylsilyldiazomethane
    UPLC ultra performance liquid chromatography
    wt weight
    μg microgram
    μL microliter
    • LC Specificity: LC Method 1:
  • The retention times (Rt) were obtained on a Waters Acquity SDS system with an Acquity BEH 1.7 μm 2.1×50 mm column. A gradient of H2O (+0.1% formic acid)/CH3CN (+0.1% formic acid) 98/2 to 2/98 was applied over 1.7 min., then held for 0.24 min. (1.0 mL/min. as solvent flow) at an oven temperature of 50° C.
    • LC Method 2:
  • The retention times (Rt) were obtained on a Waters Acquity SDS system with an Acquity BEH C18 1.7 μm 2.1×50 mm column. A gradient of H2O (+0.1% formic acid)/CH3CN (+0.1% formic acid) 98/2 to 2/98 was applied over 1.7 min., then held for 0.3 min. (1.0 mL/min. as solvent flow) at an oven temperature of 50° C.
    • LC Method 3:
  • The retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 μm, 2.1×50 mm column. A gradient of H2O (+0.1% formic acid)/CH3CN (+0.1% formic acid) 95/5 to 5/95 was applied over 1.2 min., then held for 0.5 min. (1.0 mL/min. as solvent flow) at an oven temperature of 50° C.
    • LC Method 4:
  • The retention times (Rt) were obtained on an Agilent 1100 system with an Sunfire C18 Column, 3.5 μm, 3.0×30 mm column. A gradient of H2O (+0.05% trifluoroacetic acid)/CH3CN (+0.05% trifluoroacetic acid) 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
    • LC Method 5:
  • The retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 μm, 3.0×30 mm column. A gradient of H2O (+0.05% ammonium hydroxide)/CH3CN (+0.05% ammonium hydroxide) 98/2 to 2/98 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
    • LC Method 6:
  • The retention times (Rt) were obtained on a Waters Acquity SDS system with an Acquity CSH 1.7 μm 2.1×50 mm column. A gradient of H2O (+2% CH3CN+3.75 mM ammonium acetate)/CH3CN (+5% water+3.75 mM ammonium acetate) 98/2 to 2/98 was applied over 1.7 min., then held for 0.3 min. (1.0 mL/min. as solvent flow) at an oven temperature of 50° C.
    • LC Method 7:
  • The retention times (Rt) were obtained on a Waters Acquity SDS system with an Acquity CSH 1.7 μm 2.1×50 mm column. A gradient of H2O (+3.75 mM ammonium acetate+2% CH3CN)/CH3CN 98/2 to 2/98 was applied over 1.7 min., then held for 0.3 min. (1.0 mL/min. as solvent flow) at an oven temperature of 50° C.
    • LC Method 8:
  • The retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 μm, 3.0×30 mm column. A gradient of H2O (5 mM ammonium formate, 2% CH3CN)/CH3CN 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
    • LC Method 9
  • The retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 μm, 3.0×30 mm column. A gradient of H2O (+5 mM ammonium hydroxide)/CH3CN 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
    • LC Method 10:
  • The retention times (Rt) were obtained on an Agilent 1100 system with an XBridge C18 Column, 3.5 μm, 3.0×30 mm column. A gradient of H2O (+5 mM ammonium hydroxide)/CH3CN 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
    • LC Method 11:
  • The retention times (Rt) were obtained on an Agilent 1100 system with an Sunfire C18 Column, 3.5 μm, 3.0×30 mm column. A gradient of H2O (+0.05% trifluoroacetic acid)/CH3CN (+0.05% trifluoroacetic acid) 95/5 to 5/95 was applied over 1.7 min., then held for 0.3 min. (2.0 mL/min. as solvent flow) at an oven temperature of 40° C.
    • Processes for Making Compounds of the Invention
  • The present invention also includes processes for the preparation of compounds of the invention. In the reactions described, it can be necessary to protect reactive functional groups, for example hydroxy, amino, imino, thio or carboxy groups, where these are desired in the final product, to avoid their unwanted participation in the reactions. Conventional protecting groups can be used in accordance with standard practice, for example, see T. W. Greene and P. G. M. Wuts in “Protective Groups in Organic Chemistry”, John Wiley and Sons, 1991.
  • Compounds of Formula I can be prepared by proceeding as in the following:
    • N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline
  • Figure US20160108025A1-20160421-C00017
    • Step 1: Synthesis of 2-formyl-5-methylphenyl acetate
  • Figure US20160108025A1-20160421-C00018
  • To a 0-5° C. solution of 2-hydroxy-4-methylbenzaldehyde (15 g, 110 mmol) in 250 mL of DCM was added TEA (30.7 ml, 220 mmol) followed by dropwise addition of acetyl chloride (8.65 g, 110 mmol) over 15 min. The reaction was stirred at 0-5° C. for 30 min. The reaction mixture was concentrated under reduced pressure. To this residue 100 mL of 1N HCl was added. The crude mixture was extracted with EtOAc×2. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to give a yellow oil, 2-formyl-5-methylphenyl acetate (18 g). 1H NMR (400 MHz, DMSO-d6) δ 2.34 (s, 3H), 2.40 (s, 3H), 7.13 (s, 1H), 7.31 (d, J=7.6 Hz, 1H), 7.80 (d, J=7.8 Hz, 1H), 10.01 (s, 1H).
    • Step 2: Synthesis of 2-(2,2-dibromovinyl)-5-methylphenyl acetate
  • Figure US20160108025A1-20160421-C00019
  • To a stirred mixture of 2-formyl-5-methylphenyl acetate (12.8 g, 71.8 mmol), carbon tetrabromide (47.6 g, 144 mmol), and 150 mL of DCM at 0° C. (translucent clear/yellow solution) under nitrogen was added a solution of triphenylphosphine (75 g, 287 mmol) in 140 mL of DCM dropwise over 15 min. A clear orange solution results initially. After 1 hr a purplish suspension results. The reaction was stirred for 2 hr at RT. After 2 hr 100 mL of heptane was added. The mixture was filtered to remove solids and the collected filtrate was concentrated under reduced pressure to give a dark brown gum. This was dissolved in minimal DCM and filtered through a silica gel plug which was flushed with 70% Heptane/30% EtOAc. The combined washes from the silica plug were concentrated under reduced pressure to give a yellow oil, 2-(2,2-dibromovinyl)-5-methylphenyl acetate (16.7 g). 1H NMR (400 MHz, DMSO-d6) δ 2.28 (s, 3H), 2.31 (s, 3H), 7.01 (s, 1H), 7.14 (d, J=8.0 Hz, 1H), 7.48 (s, 1H), 7.54 (d, J=8.0 Hz, 1H).
    • Step 3: Synthesis of 2-(2,2-dibromovinyl)-5-methylphenol
  • Figure US20160108025A1-20160421-C00020
  • A solution of 2-(2,2-dibromovinyl)-5-methylphenyl acetate (16.5 g, 49.4 mmol) in 100 mL of MeOH was treated with a solution of K2CO3 (10.24 g, 74.1 mmol) dissolved in 5.0 mL of water and stirred at RT. The reaction mixture immediately turned yellow and cloudy. After 30 min the mixture was concentrated under reduced pressure to remove MeOH. The crude material was diluted with water and carefully adjusted to pH 5-6 via addition of 2M HCl. The crude mixture was extracted with EtOAc×2, dried over MgSO4, filtered, and concentrated under reduced pressure to give an orange oil, 2-(2,2-dibromovinyl)-5-methylphenol (13.5 g). 1H NMR (400 MHz, DMSO-d6) δ 2.21 (s, 3H), 6.65 (d, J=8.2 Hz, 1H), 6.68 (s, 1H), 7.49 (d, J=7.9 Hz, 1H), 7.57 (s, 1H), 9.83 (s, 1H).
    • Step 4: Synthesis of 6-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00021
  • To a 500 mL 3-neck flask was added 2-(2,2-dibromovinyl)-5-methylphenol (17.7 g, 60.6 mmol), CuI (1.16 g, 6.06 mmol), Na2CO3 (12.85 g, 121 mmol) and DMF (120 mL). The reaction was heated to 80° C. for 6 hr. After 6 hr the rxn was cooled to RT and anhydrous K4Fe(CN)6 (4.47 g, 12.12 mmol), Pd(OAc)2 (2.04 g, 3.03 mmol) and PPh3 (0.32 g, 1.21 mmol) were added to the reaction and the reaction was flushed with nitrogen for 10 min. The reaction was then heated to 120° C. for 18 hr. After 18 hr the rxn was cooled to RT and diluted with EtOAc. The reaction mixture was filtered through a silica plug to remove solids and flushed with EtOAc. The collected filtrates were diluted with water and brine and extracted with EtOAc×2. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude mixture was purified via silica gel FCC, 100% Heptane—20% EtOAc/80% Heptane to give a yellow solid, 6-methylbenzofuran-2-carbonitrile (5.1 g). 1H NMR (400 MHz, DMSO-d6) δ 2.47 (s, 3H), 7.27 (ddd, J=8.2, 1.4, 0.7 Hz, 1H), 7.57 (s, 1H), 7.71 (d, J=8.1 Hz, 1H), 8.05 (d, J=1.0 Hz, 1H).
    • Step 5: Synthesis of 6-(bromomethyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00022
  • 6-methylbenzofuran-2-carbonitrile (12 g, 76 mmol), NBS (13.59 g, 76 mmol), and AIBN (1.25 g, 7.64 mmol) were dissolved in carbon tetrachloride (191 ml). The mixture was heated to reflux overnight. After 18 h the reaction was cooled to RT and concentrated under reduced pressure. The product was then crashed out using MeOH and the slurry was placed in the fridge overnight. The slurry was filtered and the collected PPT was washed with MeOH. The collected PPT was pure 6-(bromomethyl)benzofuran-2-carbonitrile (13.864 g). 1H NMR (400 MHz, DMSO-d6) δ 4.87 (s, 2H), 7.52 (dd, J=8.2, 1.4 Hz, 1H), 7.83 (d, J=8.2 Hz, 1H), 7.87 (d, J=1.5 Hz, 1H), 8.11 (d, J=1.0 Hz, 1H).
    • Step 6: Synthesis of 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00023
  • 6-(bromomethyl)benzofuran-2-carbonitrile (0.5 g, 2.12 mmol) was dissolved in DMF (21.2 ml). K2CO3 (0.44 g, 3.18 mmol) was added, followed by 3-bromo-4-(trifluoromethoxy)aniline (314 μL, 2.12 mmol), and the mixture was stirred at RT for 18 hr. The reaction was diluted with EtOAc and water. The organic layer was washed with water×6, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude mixture was diluted with DCM and silica gel was added. The mixture was concentrated under reduced pressure to dry-load material for purification. The crude mixture was purified via silica gel FCC, 100% Heptane—50% EtOAc/50% Heptane to give 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carbonitrile (651 mg). LCMS retention time=1.57 minutes (LC method 1); MS (m+1)=412.1. 1H NMR (400 MHz, DMSO-d6) δ 4.46 (d, J=6.0 Hz, 2H), 6.62 (dd, J=9.0, 2.8 Hz, 1H), 6.88-6.95 (m, 2H), 7.17 (dq, J=9.0, 1.3 Hz, 1H), 7.44 (dd, J=8.2, 1.4 Hz, 1H), 7.70 (s, 1H), 7.80 (dd, J=8.1, 0.7 Hz, 1H), 8.08 (d, J=1.0 Hz, 1H).
    • Step 7: Synthesis of N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline
  • Figure US20160108025A1-20160421-C00024
  • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carbonitrile (651 mg, 1.58 mmol), sodium azide (0.12 g, 1.90 mmol) and ammonium chloride (0.10 g, 1.90 mmol) were dissolved in DMF (15.84 ml). The mixture was stirred at RT for 18 hr. After 18 hr the rxn was not complete and the reaction was heated to 50° C. for 2 hr. The reaction was cooled to RT and diluted with water (pH ˜1). The crude material was extracted from the diluted aqueous pH=1 layer three times with a 10% MeOH/90% EtOAc mixture. The combined organic layers were washed 5× with pH=1 water to remove DMF and sodium azide, they were then washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude mixture was purified on basic HPLC (ammonium hydroxide modifier) 15-40% MeCN/Water to give N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline (413 mg). LCMS retention time=1.35 minutes (LC method 1); MS (m+1)=454.2. 1H NMR (400 MHz, DMSO-d6) δ 4.39 (d, J=5.8 Hz, 2H), 6.66 (dd, J=9.0, 2.8 Hz, 1H), 6.83 (t, J=5.9 Hz, 1H), 6.93 (d, J=2.7 Hz, 1H), 7.08 (d, J=0.9 Hz, 1H), 7.17 (dd, J=9.2, 1.1 Hz, 1H), 7.25 (dd, J=8.0, 1.3 Hz, 1H), 7.54-7.64 (m, 2H).
    • 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid
  • Figure US20160108025A1-20160421-C00025
    • Step 1: Synthesis of 2-(2-formyl-5-methylphenoxy)acetonitrile
  • Figure US20160108025A1-20160421-C00026
  • To a solution of 2-hydroxy-4-methylbenzaldehyde (12 g, 88 mmol) in 432 mL of CH3CN was added Cs2CO3 (34.5 g, 106 mmol) followed by 2-bromoacetonitrile (6.75 mL, 97 mmol), After the mixture was stirred at room temperature for 6 hr, the mixture was filtered through Celite to remove solid, washed with DCM, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel flash chromatography, 100% Heptane—20% Ethyl Acetate/80% Heptane) to give a white solid, 2-(2-formyl-5-methylphenoxy)acetonitrile (14.2 g). LCMS retention time=1.06 minutes (LC method 3); MS (m+1)=175.8. 1H NMR (400 MHz, DMSO-d6) δ 2.41 (s, 3H), 5.33 (s, 2H), 7.05 (d, J=7.8 Hz, 1H), 7.20 (s, 1H), 7.68 (s, 1H), 10.26 (d, J=0.8 Hz, 1H).
    • Step 2: Synthesis of 6-methylbenzofuran-2-carboxylic acid
  • Figure US20160108025A1-20160421-C00027
  • To a solution of 2-(2-formyl-5-methylphenoxy)acetonitrile (11.12 g, 63.5 mmol) in 244 mL of EtOH was added KOH (14.85 g, 265 mmol), and the mixture was refluxed overnight. The reaction mixture was cooled to room temperature and the solvent was evaporated until a thick slurry was obtained, which was diluted with 204 mL H2O. To the resulting solution was added concentrated HCl, a white precipitate formed, and the mixture was filtered, the solid was washed with H2O and dried under the vacuum oven at 50° C. to yield 6-methylbenzofuran-2-carboxylic acid (11.2 g). LCMS retention time=1.00 minutes (LC method 3); MS (m−1)=175.0. 1H NMR (400 MHz, DMSO-d6) δ 2.45 (s, 3H), 7.13-7.18 (m, 1H), 7.47 (s, 2H), 7.62 (d, J=8.0 Hz, 1H).
    • Step 3: Synthesis of methyl 6-methylbenzofuran-2-carboxylate
  • Figure US20160108025A1-20160421-C00028
  • To a solution of 6-methylbenzofuran-2-carboxylic acid (11 g, 62.4 mmol) in 468 mL of toluene and 156 mL of MeOH was added 2N TMS-CHN2 (46.8 mL, 94 mmol) dropwise at room temperature. The reaction was stirred at room temperature for 6 hr. The reaction was then quenched by addition of acetic acid dropwise at 0° C. until the yellow color vanished, and gas evolution ceased. The reaction was concentrated under reduced pressure, and the residue was purified by silica gel flash chromatography, 100% Heptane—10% Ethyl Acetate/90% Heptane, to give methyl 6-methylbenzofuran-2-carboxylate (7.96 g). 1H NMR (400 MHz, DMSO-d6) δ 2.46 (s, 3H), 3.88 (s, 3H), 7.20 (dd, J=8.3, 1.0 Hz, 1H), 7.53 (s, 1H), 7.67 (d, J=8.1 Hz, 1H), 7.71 (d, J=1.0 Hz, 1H).
    • Step 4: methyl 6-(bromomethyl)benzofuran-2-carboxylate
  • Figure US20160108025A1-20160421-C00029
  • Methyl 6-(bromomethyl)benzofuran-2-carboxylate was prepared as described in general bromination procedure, example 37, Step 5, starting from methyl 6-methylbenzofuran-2-carboxylate. LCMS retention time=1.24 minutes (LC method 1); MS (m+1)=269.2. 1H NMR (400 MHz, DMSO-d6) δ 3.90 (s, 3H), 4.87 (s, 2H), 7.46 (dd, J=8.2, 1.4 Hz, 1H), 7.77 (d, J=1.0 Hz, 1H), 7.80 (dd, J=8.1, 0.7 Hz, 1H), 7.84 (dt, J=1.6, 0.8 Hz, 1H).
    • Step 5: 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid
  • Figure US20160108025A1-20160421-C00030
  • Methyl 6-(bromomethyl)benzofuran-2-carboxylate (150 mg, 0.56 mmol) was dissolved in DMF (5.57 mL). K2CO3 (116 mg, 0.84 mmol) was added, followed by 3-bromo-4-(trifluoromethoxy)aniline (143 mg, 0.56 mmol), and the mixture was stirred at RT for 18 hr. At this point LiOH—H2O (117 mg, 2.79 mmol) was added to the reaction followed by 4 mL of THF and 1 mL of water and the reaction was stirred for an additional 18 hr at RT. The reaction was concentrated under reduced pressure to remove THF. The crude mixture was diluted with EtOAc and water and acidifed to pH=1. The water layer was extracted×3 with EtOAc. The combined organic layers were washed with water, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude mixture was purified on basic HPLC (ammonium hydroxide modifier) 15-40% MeCN/Water to give N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline (413 mg). LCMS retention time=1.38 minutes (LC method 1); MS (m+1)=431.2. 1H NMR (400 MHz, DMSO-d6) δ 4.38 (d, J 20=5.4 Hz, 2H), 6.65 (dd, J=9.1, 2.8 Hz, 1H), 6.87 (t, J=5.9 Hz, 1H), 6.91 (d, J=2.7 Hz, 1H), 7.02 (d, J=4.2 Hz, 1H), 7.14-7.20 (m, 1H), 7.22 (dd, J=8.0, 1.4 Hz, 1H), 7.52 (s, 1H), 7.58 (d, J=8.0 Hz, 1H).
    • N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline
  • Figure US20160108025A1-20160421-C00031
    Figure US20160108025A1-20160421-C00032
    • Step 1: Synthesis of 5-fluoro-6-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00033
  • To the solution of 5-fluoro-2-hydroxy-4-methylbenzaldehyde (500 mg, 3.24 mmol) in 10.5 ml acetonitrile in a microwave vial was added Cs2CO3 (1.268 g, 3.885 mmol), followed by 2-bromoacetonitrile (271 ul, 3.885 mmol). The reaction mixture was stirred at room temperature for 1 hr. LC/MS showed that all the starting material was converted to ring opened intermediate, 2-(4-fluoro-2-formyl-5-methylphenoxy)acetonitrile. LCMS retention time=1.19 minutes (RXNMON-Acidic:ZQ12); MS (m+1)=194.1. Then, the reaction vial was sealed, and the mixture was heated to 150° C. on microwave for 20 min. This reaction was repeated 20 times. The combined reaction mixture was filtered, washed with acetonitrile, the filtrate was concentrated. The residue was purified by silica gel flash chromatography (100% heptane—10% ethyl acetate/heptane) to give 5-fluoro-6-methylbenzofuran-2-carbonitrile (5.55 g). 1H NMR (400 MHz, DMSO-d6) δ 2.38 (d, J=2.2 Hz, 3H), 7.62 (d, J=9.3 Hz, 1H), 7.72 (d, J=6.0 Hz, 1H), 8.04 (d, J=1.0 Hz, 1H).
    • Step 2: Synthesis of 6-(bromomethyl)-5-fluorobenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00034
  • To the solution of 5-fluoro-6-methylbenzofuran-2-carbonitrile (1.44 g, 8.22 mmol) in 82 mL of CCl4 was added NBS (1.536 g, 8.63 mmol) and AIBN (0.067 g, 0.411 mmol). After the reaction mixture was refluxed overnight, the solvent was removed. The residue was purified by silica gel flash chromatography (100% heptane—7% ethyl acetate/heptane) to give 6-(bromomethyl)-5-fluorobenzofuran-2-carbonitrile (1.6 g). 1H NMR (400 MHz, DMSO-d6) δ 4.82 (d, J=1.1 Hz, 2H), 7.75 (d, J=9.5 Hz, 1H), 8.02 (d, J=5.9 Hz, 1H), 8.10 (d, J=0.86 Hz, 1H).
    • Step 3: Synthesis of 5-fluoro-6-(((4-(trifluoromethoxy)-3-(trifluoromethyl)phenyl)amino)-methyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00035
  • The mixture of 4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline (448 mg, 1.828 mmol), K2CO3 (49.0 mg, 0.354 mmol) and 6-(bromomethyl)-5-fluorobenzofuran-2-carbonitrile (387 mg, 1.523 mmol) in 2.3 ml DMF was stirred at room temperature overnight. After cooled to room temperature, the mixture was diluted with DCM, the organic layer was washed with H2O, brine and dried over Na2SO4, and concentrated. The resulting crude product was directly carried over for next step reaction without purification.
    • Step 4: Synthesis of N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline
  • Figure US20160108025A1-20160421-C00036
  • To the solution of 5-fluoro-6-(((4-(trifluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)-benzofuran-2-carbonitrile (637 mg, 1.523 mmol) in 15 mL DMF was added NH4Cl (326 mg, 6.09 mmol) and NaN3 (198 mg, 3.05 mmol). After the reaction mixture was stirred at room temperature overnight, the mixture was adjusted to pH=1 by addition of 1N HCl aqueous solution. The mixture was then diluted with AcOEt and washed with water, brine, dried over Na2SO4, and concentrated. The crude product was purified on basic HPLC (ammonium hydroxide modifier) 15-45% MeCN/Water to give N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline (194 mg). LCMS retention time=1.41 minutes (LC method 1); MS (m+1)=462.1. 1H NMR (400 MHz, DMSO-de) b 4.50 (d, J=5.2 Hz, 2H), 6.93 (dd, J=9.2, 3.0 Hz, 1H), 7.00 (br. s., 1H), 7.05 (d, J=2.8 Hz, 1H), 7.33 (d, J=9.0 Hz, 1H), 7.61-7.69 (m, 2H), 7.75 (d, J=5.7 Hz, 1H).
    • Intermediate 1: 5-(((4-propyl-3-(trifluoromethyly)phenyl)amino)methyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00037
    • Step 1: Synthesis of ethyl 2-(2-formyl-4-methylphenoxy)acetate
  • Figure US20160108025A1-20160421-C00038
  • To a solution of 2-hydroxy-5-methylbenzaldehyde (2 g, 14.69 mmol) in 22 mL of DMF was added K2CO3 (4.06 g, 29.4 mmol) under N2 at room temperature. After the mixture was stirred for 10 min, ethyl 2-bromoacetate (1.625 mL, 14.69 mmol) was added. The reaction mixture was stirred at room temperature overnight, and filtered through Celite to remove solids. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel flash chromatography, 100% Heptane—20% Ethyl Acetate/80% Heptane, to give a white solid, ethyl 2-(2-formyl-4-methylphenoxy)acetate (2.5 g). LCMS retention time=1.19 minutes (LC method 3); MS (m+1)=222.9. 1H NMR (400 MHz, DMSO-d6) δ 1.20 (t, J=7.1 Hz, 3H), 2.28 (s, 3H), 4.17 (q, J=7.2 Hz, 2H), 4.95 (s, 2H), 7.08 (d, J=8.6 Hz, 1H), 7.45 (ddd, J=8.6, 2.5, 0.6 Hz, 1H), 7.51 (d, J=2.2 Hz, 1H), 10.41 (s, 1H).
    • Step 2: Synthesis of Ethyl 5-methylbenzofuran-2-carboxylate
  • Figure US20160108025A1-20160421-C00039
  • To a solution of ethyl 2-(2-formyl-4-methylphenoxy)acetate (2.24 g, 10.08 mmol) in 15 mL of DMF was added K2CO3 (2.79 g, 20.16 mmol), the mixture was stirred under nitrogen at 90° C. for 3 hr. After cooling to room temperature, the mixture was filtered through Celite, and washed with DCM. The combined filtrate was concentrated, and the resulting residue was purified by silica gel flash chromatography, 100% Heptane—20% Ethyl Acetate/80% Heptane, to give a white solid, ethyl 5-methylbenzofuran-2-carboxylate (1.2 g). LCMS retention time=1.54 minutes (LC method 3); MS (m+1)=204.8. 1H NMR (400 MHz, DMSO-d6) δ 1.33 (t, J=7.1 Hz, 3H), 2.41 (s, 3H), 4.35 (q, J=7.1 Hz, 2H), 7.34 (dd, J=8.5, 1.4 Hz, 1H), 7.55-7.63 (m, 2H), 7.68 (d, J=0.9 Hz, 1H).
    • Step 3: Synthesis of 5-methylbenzofuran-2-carboxamide
  • Figure US20160108025A1-20160421-C00040
  • Ethyl 5-methylbenzofuran-2-carboxylate, (1.19 g, 5.83 mmol) was suspended in 20 ml of 7M NH3 in MeOH. The mixture was stirred at 50° C. in a sealed tube overnight. After cooling to room temperature, the solvent was evaporated under reduced pressure to give pure 5-methylbenzofuran-2-carboxamide, as a white solid (1.02 g). LCMS retention time=1.00 minutes (LC method 3); MS (m+1)=175.8. 1H NMR (400 MHz, DMSO-d6) b 2.40 (s, 3H), 7.45 (d, J=0.9 Hz, 1H), 7.51 (d, J=8.4 Hz, 1H), 7.53 (t, J=0.7 Hz, 1H), 7.63 (br. s., 1H), 8.05 (br. s., 1H).
    • Step 4: Synthesis of 5-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00041
  • To the suspension of 5-methylbenzofuran-2-carboxamide (5.17 g, 29.5 mmol) in 66 mL of anhydrous THF was added TEA (8.23 mL, 59.0 mmol). TFAA (6.25 mL, 44.3 mmol) was added dropwise to the above mixture at 0° C. (internal temperature did not exceed 15° C.). After stirring at 0° C. for 1 hr, the reaction was complete by TLC. The reaction mixture was poured into 610 mL of H2O, and extracted with EtOAc 3 times. The organic layer was washed with sat. NaHCO3, brine and dried over Na2SO4, filtered and concentrated under reduced pressure, and the resulting residue was purified by silica gel flash chromatography, 100% Heptane—8% Ethyl Acetate/92% Heptane, to yield 5-methylbenzofuran-2-carbonitrile (3.65 g). 1H NMR (400 MHz, DMSO-d6) b 2.42 (s, 3H), 7.42 (dd, J=8.6, 1.8 Hz, 1H), 7.59-7.67 (m, 2H), 8.03 (d, J=0.9 Hz, 1H).
    • Step 5: Synthesis of 5-(bromomethyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00042
  • 5-(Bromomethyl)benzofuran-2-carbonitrile was prepared as described in general bromination procedure, example 37, Step 5, starting from 5-methylbenzofuran-2-carbonitrile. 1H NMR (400 MHz, DMSO-d6) b 4.86 (s, 2H), 7.66-7.70 (m, 1H), 7.73-7.77 (m, 1H), 7.93 (d, J=1.6 Hz, 1H), 8.12 (d, J=0.7 Hz, 1H).
    • Step 6: Synthesis of 5-formylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00043
  • Trimethlamine-N-oxide (6.75 g, 90 mmol) was added to a solution of 5-(bromomethyl)benzofuran-2-carbonitrile (4.46 g, 18.89 mmol) in 57 mL of DMSO and 6 mL of H2O. The mixture was stirred at 70° C. for 3 hr. After the reaction was cooled to room temperature, the mixture was diluted with 72 mL of brine, and extracted with EtOAc (3×100 mL). The combined organic layers were washed with H2O (2×20 mL), brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue was purified by silica gel flash chromatography, 100% Heptane—30% Ethyl Acetate/70% Heptane, to give 5-formylbenzofuran-2-carbonitrile (1.5 g). 1H NMR (400 MHz, DMSO-d6) δ 7.96 (d, J=8.7 Hz, 1H), 8.12 (dd, J=8.7, 1.7 Hz, 1H), 8.30 (d, J=0.9 Hz, 1H), 8.46 (dd, J=1.6, 0.6 Hz, 1H), 10.11 (s, 1H).
    • Step 7: Synthesis of 5-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00044
  • 5-Formylbenzofuran-2-carbonitrile (168 mg, 0.98 mmol) was added to 2 mL of TFE and stirred at 35-40° C. After 5 min, the solution became clear, 4-propyl-3-(trifluoromethyl)aniline (199 mg, 0.982 mmol) was added, and a yellow precipitate formed. The mixture was vigorously stirred at the same temperature for 0.5 hr, NaBH4 (44.6 mg, 1.18 mmol) was added and the reaction was stirred at this temperature for another 0.5 hr. LCMS indicated the reaction was complete, the mixture was filtered, and the residue was washed with TFE (2 mL). The solvent was concentrated under reduced pressure and the crude product was purified by silica gel flash chromatography, 100% Heptane—10% Ethyl Acetate/90% Heptane, to give 5-(((4-propyl-3 (trifluoromethyl)phenyl)amino)-methyl)benzofuran-2-carbonitrile (243 mg). LCMS retention time=1.76 minutes (LC method 3); MS (m+1)=358.8. 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J=7.3 Hz, 3H), 1.48 (sxt, J=7.5 Hz, 2H), 2.47 (br. s., 2H) 4.41 (d, J=6.0 Hz, 2H), 6.64 (t, J=6.1 Hz, 1H), 6.74 (dd, J=8.4, 2.4 Hz, 1H), 6.86 (d, J=2.5 Hz, 1H), 7.10 (d, J=8.4 Hz, 1H), 7.59 (dd, J=8.7, 1.7 Hz, 1H), 7.71 (d, J=8.7 Hz, 1H), 7.78 (d, J=1.0 Hz, 1H), 8.09 (d, J=0.9 Hz, 1H).
    • Intermediate 2: 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-3-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00045
    • Step 1: Synthesis of methyl 6-bromo-3-methylbenzofuran-2-carboxylate
  • Figure US20160108025A1-20160421-C00046
  • To a suspension of 6-bromo-3-methylbenzofuran-2-carboxylic acid (5 g, 19.6 mmol) in 196 mL of MeOH was added SOCl2 (2.9 mL, 39.2 mmol). After the mixture was heated to reflux for 1 hr, the reaction solution became clear, and the color changed to green. The mixture was concentrated to remove part of solvent, and the color of the solution changed to yellow. After cooling to room temperature a white PPT formed, and the suspension was filtered, and the solid was washed with small amounts of EtOAc. The solid was dried under vacuum at 50° C. to give pure methyl 6-bromo-3-methylbenzofuran-2-carboxylate (3.56 g). LCMS retention time=1.58 minutes (LC method 3); MS (m+1)=270.9. 1H NMR (400 MHz, CHLOROFORM-d) δ 2.59 (s, 3H), 3.99 (s, 3H), 7.41-7.47 (m, 1H), 7.48-7.53 (m, 1H), 7.72 (d, J=1.5 Hz, 1H).
    • Step 2 and 3: Synthesis of methyl 2-carbamoyl-3-methylbenzofuran-6-carboxylate
  • Figure US20160108025A1-20160421-C00047
  • Methyl 6-bromo-3-methylbenzofuran-2-carboxylate (3.65 g, 13.56 mmol) was converted to 6-bromo-3-methylbenzofuran-2-carboxamide (2.99 g) by the method as described in preparation of Intermediate 1, Step 3. LCMS retention time=1.05 minutes (RXNMON-Acidic:SQ4); MS (m+1)=256.2.
  • To a mixture of 6-bromo-3-methylbenzofuran-2-carboxamide (2.99 g, 11.77 mmol) in 238 mL of DMSO and 119 mL of MeOH was added TEA (8.20 mL, 58.8 mmol) followed by Pd(OAc)2 (264 mg, 1.18 mmol) and DPPF (6.52 g, 11.77 mmol). The resulting mixture was purged with CO gas and heated at 85° C. under 1 atm of CO gas for 3 hr. The reaction was monitored by LCMS. After the solution was cooled to room temperature, the reaction was diluted with 600 mL of EtOAc and 600 mL of water. The organic layer was separated and the aqueous layer was further extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel flash chromatography, 100% Heptane—50% Ethyl Acetate/50% Heptane to give methyl 2-carbamoyl-3-methylbenzofuran-6-carboxylate (2.19 g). LCMS retention time=1.26 minutes (LC method 3); MS (m+1)=234.0. 1H NMR (400 MHz, DMSO-d6) δ 2.54 (s, 3H), 3.90 (s, 3H), 7.75 (br. s., 1H), 7.85-7.90 (m, 1H), 7.90-7.96 (m, 1H), 8.01 (br. s., 1H), 8.06 (s, 1H).
    • Step 4: Synthesis of methyl 2-cyano-3-methylbenzofuran-6-carboxylate
  • Figure US20160108025A1-20160421-C00048
  • 2-Cyano-3-methylbenzofuran-6-carboxylate was prepared as described in Intermediate 1, Step 4, starting from methyl 2-carbamoyl-3-methylbenzofuran-6-carboxylate. LCMS retention time=1.52 minutes (LC method 3); MS (m+1)=216.0. 1H NMR (400 MHz, DMSO-d6) 2.48 (s, 3H), 3.90-3.92 (m, 3H), 7.96-8.03 (m, 2H), 8.22-8.25 (m, 1H).
    • Step 5: Synthesis of 6-(hydroxymethyl)-3-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00049
  • 2-Cyano-3-methylbenzofuran-6-carboxylate (540 mg, 2.51 mmol) was dissolved in 17 mL of EtOH, and CaCl2 (557 mg, 5.02 mmol) was added and the mixture was briefly stirred in the ultrasound bath. Then the mixture was cooled to 0° C. and a solution of NaBH4 (380 mg, 10.04 mmol) in 17 mL of THF was added. The mixture was stirred at 0° C. for 1.5 hr, and then 1N HCl was carefully added. The organic layer was separated, and the aqueous phase was extracted with DCM (4×7 mL), the combined organic phases were dried over Na2SO4, filtered off and evaporated under reduced pressure. The crude product was purified by silica gel flash chromatography 100% DCM—7% MeOH/93% DCM to give 6-(hydroxymethyl)-3-methylbenzofuran-2-carbonitrile (233 mg). 1H NMR (400 MHz, DMSO-d6) δ 2.44 (s, 3H), 4.65 (d, J=5.8 Hz, 2H), 5.42 (t, J=5.8 Hz, 1H), 7.35-7.42 (m, 1H), 7.60 (s, 1H), 7.77 (d, J=8.2 Hz, 1H).
    • Step 6: Synthesis of 6-formyl-3-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00050
  • To a solution of 6-(hydroxymethyl)-3-methylbenzofuran-2-carbonitrile (116 mg, 0.62 mmol) in 6 mL of DCM was added NaHCO3 (125 mg, 1.49 mmol), followed by Dess-Martin periodinane (315 mg, 0.74 mmol). The reaction was stirred at room temperature for 1 hr. The reaction was quenched by addition of 2 mL of sat. NaHCO3 and 2 mL of sat. Na2S2O3 and stirred for 30 min. The reaction mixture was extracted with DCM (3×50 mL), the organic layer was washed with H2O, brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by silica gel flash chromatography 100% Heptane—50% Ethyl Acetate/50% Heptane) to give 6-formyl-3-methylbenzofuran-2-carbonitrile (96 mg). 1H NMR (400 MHz, DMSO-d6) δ 2.51 (br. s., 3H), 7.97 (dd, J=8.1, 1.2 Hz, 1H), 8.04-8.09 (m, 1H), 8.27 (s, 1H), 10.14 (s, 1H).
    • Step 7: Synthesis of 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-3-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00051
  • The title compound was prepared as described in general reductive amination procedure, starting from 3-bromo-4-(trifluoromethoxy)aniline and 6-formyl-3-methylbenzofuran-2-carbonitrile, Intermediate 4. LCMS retention time=1.64 minutes (LC method 3); MS (m+1)=426.0.
    • General Reductive Amination Procedure Synthesis of 5-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00052
  • 5-Formylbenzofuran-2-carbonitrile (168 mg, 0.98 mmol) was added to 2 mL of TFE and stirred at 35-40° C. After 5 min, the solution became clear, 4-propyl-3-(trifluoromethyl)aniline (199 mg, 0.982 mmol) was added, and a yellow precipitate formed. The mixture was vigorously stirred at the same temperature for 0.5 hr, NaBH4 (44.6 mg, 1.18 mmol) was added and the reaction was stirred at this temperature for another 0.5 hr. The mixture was then filtered, and the residue was washed with TFE (2 mL). The solvent was concentrated under reduced pressure and the crude product was purified by silica gel flash chromatography, 100% Heptane—10% Ethyl Acetate/90% Heptane, to give 5-(((4-propyl-3 (trifluoromethyl)phenyl)amino)-methyl)benzofuran-2-carbonitrile (243 mg). LCMS retention time=1.76 minutes (LC method 3); MS (m+1)=358.8. 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J=7.3 Hz, 3H), 1.48 (sxt, J=7.5 Hz, 2H), 2.47 (br. s., 2H) 4.41 (d, J=6.0 Hz, 2H), 6.64 (t, J=6.1 Hz, 1H), 6.74 (dd, J=8.4, 2.4 Hz, 1H), 6.86 (d, J=2.5 Hz, 1H), 7.10 (d, J=8.4 Hz, 1H), 7.59 (dd, J=8.7, 1.7 Hz, 1H), 7.71 (d, J=8.7 Hz, 1H), 7.78 (d, J=1.0 Hz, 1H), 8.09 (d, J=0.9 Hz, 1H).
    • General Bromomethylbenzofuran Aniline Coupling Reaction Synthesis of 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00053
  • 6-(bromomethyl)benzofuran-2-carbonitrile (0.5 g, 2.12 mmol) was dissolved in DMF (21.2 ml). K2CO3 (0.44 g, 3.18 mmol) was added, followed by 3-bromo-4-(trifluoromethoxy)aniline (314 μL, 2.12 mmol), and the mixture was stirred at RT for 18 hr. The reaction was diluted with EtOAc and water. The organic layer was washed with water×6, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude mixture was diluted with DCM and silica gel was added. The mixture was concentrated under reduced pressure to dry-load material for purification. The crude mixture was purified via silica gel FCC, 100% Heptane—50% EtOAc/50% Heptane to give 6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carbonitrile (651 mg). LCMS retention time=1.57 minutes (LC method 1); MS (m+1)=412.1. 1H NMR (400 MHz, DMSO-d6) δ 4.46 (d, J=6.0 Hz, 2H), 6.62 (dd, J=9.0, 2.8 Hz, 1H), 6.88-6.95 (m, 2H), 7.17 (dq, J=9.0, 1.3 Hz, 1H), 7.44 (dd, J=8.2, 1.4 Hz, 1H), 7.70 (s, 1H), 7.80 (dd, J=8.1, 0.7 Hz, 1H), 8.08 (d, J=1.0 Hz, 1H).
    • Intermediate 3: Ethyl 2-(5-methyl-2-(2,2,2-trifluoroacetyl)phenoxy)acetate
  • Figure US20160108025A1-20160421-C00054
    • Step 1: Synthesis of 2,2,2-trifluoro-1-(2-hydroxy-4-methylphenyl)ethanone
  • Figure US20160108025A1-20160421-C00055
  • To a pre-cooled (0° C.) solution of m-cresol (5.84 mL, 83 mmol) in 333 mL of DCE was added TFAA (16.75 mL, 119 mmol) over 20 min. Aluminum trichloride (36.2 g, 271 mmol) was then added portion-wise over 30 min. The reaction mixture was gradually warmed to room temperature over 2 hr and then heated at 40° C. for 19 hr. The reaction mixture was cooled to room temperature and poured over ice water. The resulting mixture was extracted with DCM (2×50 mL), the combined organic layers were washed with a sat. NaHCO3 solution (1500 mL), followed by a brine solution (1500 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue was purified by silica gel flash chromatography, 100% Heptane—5% Ethyl Acetate/95% Heptane) to give 2,2,2-trifluoro-1-(2-hydroxy-4-methylphenyl)ethanone (6.77 g). 1H NMR (400 MHz, CHLOROFORM-d) δ 2.41 (s, 3H), 6.82 (dd, J=8.5, 1.1 Hz, 1H), 6.90 (s, 1H), 7.70 (dq, J=8.5, 2.2 Hz, 1H), 11.11 (s, 1H).
    • Step 2: Synthesis of ethyl 2-(5-methyl-2-(2,2,2-trifluoroacetyl)phenoxy)acetate
  • Figure US20160108025A1-20160421-C00056
  • The title compound was prepared as described in Intermediate 1, Step 1, starting from 2,2,2-trifluoro-1-(2-hydroxy-4-methylphenyl)ethanone. LCMS retention time=1.33 minutes (LC method 1); MS (m+1)=291.3. 1H NMR (400 MHz, CHLOROFORM-d) δ 1.30 (t, J=7.1 Hz, 3H), 2.41 (s, 3H), 4.28 (d, J=7.2 Hz, 2H), 4.72 (s, 2H), 6.71 (s, 1H), 6.93 (dd, J=8.0, 0.6 Hz, 1H), 7.64 (d, J=8.0 Hz, 1H).
    • Step 3: Synthesis of ethyl 6-methyl-3-(trifluoromethyl)benzofuran-2-carboxylate
  • Figure US20160108025A1-20160421-C00057
  • The mixture of ethyl 2-(5-methyl-2-(2,2,2-trifluoroacetyl)phenoxy)acetate (7.3 g, 25.2 mmol) and pre-oven dried K2CO3 (5.21 g, 37.7 mmol) in 25 mL of CH3CN in sealed tube was heated and stirred at 90° C. for two days. After cooling to room temperature, the reaction was filtered, and the solid was washed with anhydrous CH3CN. The combined filtrate was concentrated to dryness under reduced pressure. The resulting residue was purified by silica gel flash chromatography, 100% Heptane—2% Ethyl Acetate/98% Heptane, to give ethyl 6-methyl-3-(trifluoromethyl)benzofuran-2-carboxylate (2.35 g). LCMS retention time=1.52 minutes (LC method 1); MS (m+1)=273.3. 1H NMR (400 MHz, CHLOROFORM-d) 1.45 (t, J=7.1 Hz, 3H), 2.53 (s, 3H), 4.50 (q, J=7.2 Hz, 2H), 7.24 (dd, J=8.3, 0.9 Hz, 1H), 7.43 (d, J=0.6 Hz, 1H), 7.69-7.77 (m, 1H).
    • Intermediate 4: 5-(1-((3-chloro-4-propylphenyl)amino)ethyl)benzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00058
    • Step 1: Synthesis of 5-acetylbenzofuran-2-carboxamide
  • To a suspension of benzofuran-2-carboxamide (4.07 g, 25.3 mmol) in 200 mL of DCM was added acetyl chloride (5.34 mL, 75 mmol). AlCl3 (13.5 g, 101 mmol) was added to above mixture while stirring in small portions, and the solution became clear. The reaction was stirred at room temperature for 19 hr. The reaction mixture was added to 200 mL 0.1N HCl, then extracted with DCM (3×150 mL), the organic layer was washed with H2O, brine and dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography, 50% Ethyl Acetate/50% Heptane—75% Ethyl Acetate/25% Heptane, to give 5-acetylbenzofuran-2-carboxamide (2.69 g). LCMS retention time=0.81 minutes (LC method 3); MS (m+1)=203.9. 1H NMR (400 MHz, DMSO-d6) δ 2.65 (s, 3H), 7.67 (d, J=0.9 Hz, 1H), 7.72-7.78 (m, 2H), 8.02-8.07 (m, 1H), 8.20 (br. s., 1H), 8.46 (d, J=1.7 Hz, 1H).
    • Step 2: Synthesis of 5-acetylbenzofuran-2-carbonitrile
  • 5-Acetylbenzofuran-2-carbonitrile was prepared as described in Intermediate 1, Step 4, starting from 5-acetylbenzofuran-2-carboxamide. LCMS retention time=1.05 minutes (LC method 1); MS (m+1)=186.1. 1H NMR (400 MHz, DMSO-d6) δ 2.66 (s, 3H), 7.87 (d, J=8.9 Hz, 1H), 8.17 (dd, J 25=8.8, 1.8 Hz, 1H), 8.24 (d, J=0.9 Hz, 1H), 8.51 (d, J=1.8 Hz, 1H).
    • Step 3: Synthesis of (±) 5-(1-((3-chloro-4-propylphenyl)amino)ethyl)benzofuran-2-carbonitrile
  • A mixture of 5-acetylbenzofuran-2-carbonitrile (64 mg, 0.35 mmol), 3-chloro-4-propylaniline (140 mg, 0.82 mmol) and Ti(OiPr)4 (205 μL, 0.69 mmol) was heated to 50° C. for 3 hr, then 60° C. for 2 hr. The reaction mixture was diluted with 10 mL of DCM, and celite was added to the solution (enough to equal the volume of the mixture). The reaction was quenched with 5 mL of sat. NaHCO3:H2O=1:1, and filtered. The separated organic layer was washed with H2O, brine and dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was dissolved in 1.4 mL of TFE and NaBH4 (15.69 mg, 0.415 mmol) was added. The reaction was stirred at 40° C. for 2 hr. After cooling to room temperature, the reaction mixture was diluted with 50 mL of DCM, which was then washed with H2O, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography, 100% Heptane—30% Ethyl Acetate/70% Heptane, to give (±) 5-(1-((3-chloro-4-propylphenyl)amino)ethyl)benzofuran-2-carbonitrile (113 mg). LCMS retention time=1.66 minutes (LC method 1); MS (m+1)=339.3.
    • Intermediate 5: 5-formyl-3-methyl benzofuran-2-carboxamide
  • Figure US20160108025A1-20160421-C00059
    • Step 1: Synthesis of ethyl 5-formyl-3-methylbenzofuran-2-carboxylate
  • Figure US20160108025A1-20160421-C00060
  • To a 10 mL flask, fitted with a inlet needle, was placed PdCl2(PPh3)2 (179 mg, 0.25 mmol), ethyl 5-bromo-3-methylbenzofuran-2-carboxylate (3.6 g, 12.72 mmol) and sodium formate (1.30 g, 19.07 mmol). After the mixture was degassed by CO gas, 13 mL of DMF was added by syringe, and a slow stream of CO was passed into the suspension. The mixture was vigorously stirred at 110° C. for 5 hr. After the reaction mixture was cooled to room temperature 2 mL of 1N NaOH was added to the reaction mixture and the mixture was diluted with EtOAc. The separated organic layer was washed with H2O and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography, 100% Heptane—15% Ethyl Acetate/85% Heptane, to yield 5-formyl-3-methylbenzofuran-2-carboxylate (1.33 g). LCMS retention time=1.15 minutes (LC method 1); MS (m+1)=233.2. 1H NMR (400 MHz, DMSO-d6) δ 1.36 (t, J=7.1 Hz, 3H), 2.62 (s, 3H), 4.38 (q, J=7.1 Hz, 2H), 7.88 (d, J=8.7 Hz, 1H), 8.06 (dd, J=8.7, 1.71 Hz, 1H), 8.45 (dd, J=1.6, 0.6 Hz, 1H), 10.11 (s, 1H).
    • Step 2: Synthesis of 5-formyl-3-methylbenzofuran-2-carboxamide
  • Figure US20160108025A1-20160421-C00061
  • 5-Formyl-3-methylbenzofuran-2-carboxamide was prepared as described in Intermediate 1, Step 3, starting from 5-formyl-3-methylbenzofuran-2-carboxylate. LCMS retention time=1.17 minutes (LC method 1); MS (m+1)=203.9. 1H NMR (400 MHz, DMSO-d6) δ 2.58 (s, 3H), 7.72 (br. s., 1H), 7.76 (d, J=8.6 Hz, 1H), 8.01 (dd, J=8.6, 1.7 Hz, 2H), 8.37 (d, J=1.2 Hz, 1H), 10.10 (s, 1H).
    • Intermediate 6 4-Propyl-3-(trifluoromethyl)aniline
  • Figure US20160108025A1-20160421-C00062
    • Step 1: Synthesis of 4-propyl-3-(trifluoromethyl)aniline
  • Figure US20160108025A1-20160421-C00063
  • To a solution of 1-allyl-4-nitro-2-(trifluoromethyl)benzene (750 mg, 3.24 mmol) in 18 mL of THF and 3.6 mL of H2O was added 10% Pd/C (250 mg, 3.24 mmol). The reaction was stirred at room temperature under an H2 balloon for 24 hr. After filtering to remove Pd/C, the reaction solution was concentrated under reduced pressure. The residue was purified by silica gel flash chromatography, 100% Heptane—10% Ethyl Acetate/90% Heptane, to give 4-propyl-3-(trifluoromethyl)aniline (440 mg). LCMS retention time=1.53 minutes (LC method 3); MS (m+1)=203.8. 1H NMR (400 MHz, DMSO-d6) δ 0.93 (t, J=7.4 Hz, 3H), 1.54 (sxt, J=7.6 Hz, 2H), 2.51-2.56 (m, 2H), 5.66 (s, 2H), 6.44 (dd, J=8.5, 1.9 Hz, 1H), 6.52 (d, J=2.1 Hz, 1H), 7.24 (d, J=8.6 Hz, 1H).
    • Intermediate 7 3-Fluoro-4-propylaniline
  • Figure US20160108025A1-20160421-C00064
    • Step 1: Synthesis of 1-allyl-2-fluoro-4-nitrobenzene
  • Figure US20160108025A1-20160421-C00065
  • 2-Fluoro-4-nitroaniline (5 g, 32.0 mmol) was added to a solution of 3-bromoprop-1-ene (41.5 mL, 480 mmol) and tert-butyl nitrite (5.76 mL, 48.0 mmol) in 32 mL of degassed anhydrous CH3CN at 18-19° C. under nitrogen. At the end of the addition of the arylamine, another half-equivalent of tert-butyl nitrite (1.180 mL, 16.01 mmol) was added; the reaction was stirred at room temperature for 1 hr. The reaction was concentrated under reduced pressure to remove the volatile material. The residue was purified by silica gel flash chromatography, 100% Heptane—5% Ethyl Acetate/95% Heptane, to give 1-allyl-2-fluoro-4-nitrobenzene (2.98 g). 1H NMR (400 MHz, DMSO-d6) δ 3.51 (dd, J=6.4, 1.1 Hz, 2H), 5.05-5.16 (m, 2H), 5.96 (ddt, J=16.8, 10.2, 6.6, 6.6 Hz, 1H), 7.56-7.62 (m, 1H), 8.03-8.11 (m, 2H).
    • Step 2: Synthesis of 3-fluoro-4-propylaniline
  • Figure US20160108025A1-20160421-C00066
  • 3-fluoro-4-propylaniline was prepared as described in Intermediate 6, step 1, starting from 1-allyl-2-fluoro-4-nitrobenzene. LCMS retention time=1.21 minutes (LC method 1); MS (m+1)=154.1. 1H NMR (400 MHz, DMSO-d6) δ 0.85 (t, J=7.3 Hz, 3H), 1.47 (sxt, J=7.4 Hz, 2H), 2.37 (t, J=7.6 Hz, 2H), 5.15 (s, 2H), 6.24-6.32 (m, 2H), 6.81-6.88 (m, 1H).
    • Intermediate 8 3-Methoxy-4-propylaniline
  • Figure US20160108025A1-20160421-C00067
    • Step 1: Synthesis of 1-allyl-2-methoxy-4-nitrobenzene
  • Figure US20160108025A1-20160421-C00068
  • 1-Allyl-2-methoxy-4-nitrobenzene was prepared as described in Intermediate 7, step 1, starting from 2-methoxy-4-nitroaniline. 1H NMR (400 MHz, DMSO-d6) δ 3.41 (d, J=6.8 Hz, 2H), 3.92 (s, 3H), 5.04-5.07 (m, 1H), 5.08-5.11 (m, 1H), 5.89-6.00 (m, 1H), 7.40 (d, J=8.3 Hz, 1H), 7.74 (d, J=2.3 Hz, 1H), 7.81 (dd, J=8.3, 2.3 Hz, 1H).
    • Step 2: Synthesis of 3-methoxy-4-propylaniline
  • Figure US20160108025A1-20160421-C00069
  • 3-Methoxy-4-propylaniline was prepared as described in Intermediate 6, step 1, starting from 1-allyl-2-methoxy-4-nitrobenzene. LCMS retention time=1.08 minutes (LC method 3); MS (m+1)=165.8. 1H NMR (400 MHz, DMSO-d6) δ 0.84 (t, J=7.5 Hz, 3H), 1.43 (sxt, J=7.4 Hz, 2H), 2.30-2.36 (m, 2H), 3.66 (s, 3H), 4.85 (br. s., 2H), 6.05 (dd, J=7.8, 2.0 Hz, 1H), 6.18 (d, J=2.0 Hz, 1H), 6.71 (d, J=7.8 Hz, 1H).
    • Intermediate 9 4-Propyl-3-(trifluoromethoxy)aniline
  • Figure US20160108025A1-20160421-C00070
    • Step 1: Synthesis of 4-propyl-3-(trifluoromethoxy)aniline
  • Figure US20160108025A1-20160421-C00071
  • 4-Propyl-3-(trifluoromethoxy)aniline was prepared as described in Intermediate 6, step 1, starting from 1-allyl-4-nitro-2-(trifluoromethoxy)benzene. LCMS retention time=1.50 minutes (LC method 3); MS (m+1)=219.8. 1H NMR (400 MHz, DMSO-d6) δ 0.86 (t, J=7.3 Hz, 3H), 1.47 (sxt, J=7.4 Hz, 2H), 2.36-2.43 (m, 2H), 5.29 (br. s., 2H), 6.45-6.50 (m, 2H), 6.96 (d, J=8.8 Hz, 1H).
    • Intermediate 10 3-Chloro-5-methyl-4-propylaniline
  • Figure US20160108025A1-20160421-C00072
    • Step 1: Synthesis of 2-allyl-1-chloro-3-methyl-5-nitrobenzene
  • Figure US20160108025A1-20160421-C00073
  • 2-Allyl-1-chloro-3-methyl-5-nitrobenzene was prepared as described in Intermediate 7, step 1, starting from 2-chloro-6-methyl-4-nitroaniline. 1H NMR (400 MHz, DMSO-d6) δ 2.44 (s, 3H), 3.61 (d, J=4.0 Hz, 2H), 4.90 (dd, J=17.2, 1.7 Hz, 1H), 5.07 (dq, J=10.2, 1.6 Hz, 1H), 5.83-5.94 (m, 1H), 8.08 (d, J=2.2 Hz, 1H), 8.12 (d, J=2.3 Hz, 1H).
    • Step 2: Synthesis of 3-chloro-5-methyl-4-propylaniline
  • Figure US20160108025A1-20160421-C00074
  • A solution of 2-allyl-1-chloro-3-methyl-5-nitrobenzene (450 mg, 2.13 mmol) in 43 mL of MeOH was put on an H-cube with a Ra—Ni cartridge, the reaction was at room temperature and under 2 atm of H2 for 3 hr. The reaction was concentrated under reduced pressure. The residue was purified by silica gel flash chromatography, 100% Heptane—15% Ethyl Acetate/85% Heptane, to give 3-chloro-5-methyl-4-propylaniline (212 mg). LCMS retention time=1.34 minutes (LC method 1); MS (m+1)=184.1. 1H NMR (400 MHz, DMSO-d6) δ 0.92 (t, J=7.3 Hz, 3H), 1.34-1.48 (m, 2H), 2.16 (s, 3H), 2.48-2.52 (m, 2H), 5.03 (s, 2H), 6.32 (d, J=1.8 Hz, 1H), 6.43 (d, J=2.2 Hz, 1H).
    • Intermediate 11 3-(prop-1-en-2-yl)-4-(trifluoromethoxy)aniline
  • Figure US20160108025A1-20160421-C00075
    • Step 1: Synthesis of 4-nitro-2-(prop-1-en-2-yl)-1-(trifluoromethoxy)benzene
  • Figure US20160108025A1-20160421-C00076
  • 2-bromo-4-nitro-1-(trifluoromethoxy)benzene (0.56 g, 1.97 mmol), 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane (0.50 g, 2.96 mmol), PdCl2(dppf).CH2Cl2 adduct (0.16 g, 0.20 mmol), and Na2CO3 (0.63 g, 5.92 mmol) were combined in a 20 mL microwave vial and DME (15.78 mL) and Water (3.94 mL) were added. The mixture was stirred at RT for 6 s and then heated to 120° C. in the microwave for 30 min. The crude mixture was diluted with EtOAc and Water. The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The crude was diluted with DCM and silica gel was added. The mixture was concentrated under reduced pressure to dry-load material for purification. The crude was purified via silica gel FCC, 100% Heptane—100% EtOAc to give 4-nitro-2-(prop-1-en-2-yl)-1-(trifluoromethoxy)benzene (456 mg). 1H NMR (400 MHz, DMSO-d6) b 2.08-2.13 (m, 3H), 5.21 (p, J=1.0 Hz, 1H), 5.43 (p, J 25=1.5 Hz, 1H), 7.68 (dq, J=9.0, 1.6 Hz, 1H), 8.21 (d, J=2.9 Hz, 1H), 8.28 (dd, J=9.0, 2.9 Hz, 1H).
    • Step 2: Synthesis of 3-(prop-1-en-2-yl)-4-(trifluoromethoxy)aniline
  • Figure US20160108025A1-20160421-C00077
  • To a solution of 4-nitro-2-(prop-1-en-2-yl)-1-(trifluoromethoxy)benzene (275 mg, 1.11 mmol) in toluene (9.85 mL) was added iron (1.24 g, 22.25 mmol) and concentrated HCl (3.38 μL, 0.11 mmol) (3 drops). The mixture was stirred vigorously under reflux and water (0.20 mL, 11.13 mmol) was added and the rxn was stirred at reflux for 2 hr. The crude mixture was filtered through celite and concentrated under reduced pressure. The crude was diluted with EtOAc and dried with Na2SO4, filtered and concentrated under reduced pressure to give 3-(prop-1-en-2-yl)-4-(trifluoromethoxy)aniline (230 mg). LCMS retention time=1.46 minutes (LC method 5); MS (m+1)=218.2.
    • Intermediate 12 5-fluoro-6-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00078
  • To a solution of 5-fluoro-2-hydroxy-4-methylbenzaldehyde (500 mg, 3.24 mmol) in 10.5 ml of acetonitrile in a microwave vial was added Cs2CO3 (1.268 g, 3.885 mmol), followed by 2-bromoacetonitrile (271 ul, 3.885 mmol). The reaction mixture was stirred at room temperature for 1 hr. LC/MS showed that all the starting material was converted to ring opened intermediate, 2-(4-fluoro-2-formyl-5-methylphenoxy)acetonitrile. LCMS retention time=1.19 minutes (RXNMON-Acidic:ZQ12); MS (m+1)=194.1. Then, the reaction vial was sealed, and the mixture was heated to 150° C. on microwave for 20 min. This reaction was repeated 20 times. The combined reaction mixture was filtered, washed with acetonitrile, the filtrate was concentrated. The residue was purified by silica gel flash chromatography (100% heptane—10% ethyl acetate/heptane) to give 5-fluoro-6-methylbenzofuran-2-carbonitrile (5.55 g). 1H NMR (400 MHz, DMSO-d6) δ 2.38 (d, J=2.2 Hz, 3H) 7.62 (d, J=9.3 Hz, 1H) 7.72 (d, J=6.0 Hz, 1H) 8.04 (d, J=1.0 Hz, 1H).
    • Intermediate 13 Synthesis of 6-fluoro-5-methylbenzofuran-2-carbonitrile
  • Figure US20160108025A1-20160421-C00079
  • 6-Fluoro-5-methylbenzofuran-2-carbonitrile was prepared as described in Intermediate 12 starting from 4-fluoro-2-hydroxy-5-methylbenzaldehyde, 1H NMR (400 MHz, DMSO-d6) δ 2.31-2.36 (m, 3H) 7.67-7.77 (m, 2H) 8.07 (d, J=1.0 Hz, 1H).
  • Compounds of the present invention are made with the preceding procedures and intermediates and are exemplified below in Table 1.
  • TABLE 1
    LCMS LCMS
    Example Compound Characterization RT(min) Method
    1
    Figure US20160108025A1-20160421-C00080
         		MS (m + 1) = 419.3; 1H NMR (400 MHz, DMSO-d6) δ 3.67 (s, 3H), 4.30-4.40 (m, 2H), 6.51 (dd, J = 13.6, 2.7 Hz, 1H), 6.59-6.67 (m, 2H), 7.11 (d, J = 0.9 Hz, 1H), 7.25 (dd, J = 8.2, 1.3 Hz, 1H), 7.56-7.63 (m, 2H). 1.23 1
    2
    Figure US20160108025A1-20160421-C00081
         		MS (m + 1) = 432.4; 1H NMR (400 MHz, DMSO-d6) δ 1.26 (t, J = 7.0 Hz, 3H), 3.88 (q, J = 7.0 Hz, 2H), 4.35 (d, J = 5.2 Hz, 2H), 6.50 (dd, J = 13.4, 2.6 Hz, 1H), 6.61 (t, J = 6.0 Hz, 1H), 6.66 (dd, J = 2.7, 1.6 Hz, 1H), 7.15 (d, J = 0.9 Hz, 1H), 7.25 (dd, J = 7.9, 1.4 1.31 1
    Hz, 1H), 7.61 (d, J = 7.9 Hz,
    2H).
    3
    Figure US20160108025A1-20160421-C00082
         		MS (m + 1) = 439.1; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (d, J = 5.8 Hz, 2H), 6.69 (dd, J = 8.8, 2.3 Hz, 1H), 7.02 (d, J = 2.2 Hz, 1H), 7.08 (d, J = 0.9 Hz, 1H), 7.24 (dd, J = 8.0, 1.3 Hz, 1H), 7.28 (t, J = 11.2, 5.8 Hz, 1H), 7.44 (d, J = 8.7 Hz, 1H), 7.57-7.62 (m, 2H). 1.32 1
    4
    Figure US20160108025A1-20160421-C00083
         		MS (m + 1) = 516.1; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (d, J = 5.9 Hz, 2H), 6.89 (t, J = 73.2 Hz, 1H), 7.16 (d, J = 1.0 Hz, 1H), 7.26 (dd, J = 7.9, 1.4 Hz, 1H), 7.58-7.65 (m, 2H). 1.31 1
    5
    Figure US20160108025A1-20160421-C00084
         		MS (m + 1) = 440.2; 1H NMR (400 MHz, DMSO-d6) δ 1.30 (t, J = 7.0 Hz, 3H), 3.88 (q, J = 7.1 Hz, 2H), 4.44 (d, J = 4.9 Hz, 2H), 6.61-6.70 (m, 3H), 7.65 (s, 1H), 7.74 (s, 1H), 7.96 (s, 1H). 1.46 1
    6
    Figure US20160108025A1-20160421-C00085
         		MS (m + 1) = 478.2; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (d, J = 5.1 Hz, 2H), 6.84-6.91 (m, 1H), 7.02- 7.11 (m, 2H), 7.33 (d, J = 9.1 Hz, 1H), 7.67 (s, 1H), 7.76 (s, 1H), 7.98 (s, 1H). 1.48 1
    7
    Figure US20160108025A1-20160421-C00086
         		MS (m + 1) = 444.0; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (d, J = 5.8 Hz, 2H), 6.54-6.64 (m, 2H), 7.35- 7.44 (m, 2H), 7.65 (s, 1H), 7.75 (s, 1H), 7.97 (s, 1H). 1.71 4
    8
    Figure US20160108025A1-20160421-C00087
         		MS (m + 1) = 458.2; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (s, 2H), 4.61 (q, J = 8.9 Hz, 2H), 6.42 (br. s., 1 H), 6.54 (dd, J = 8.9, 2.8 Hz, 1H), 6.71 (d, J = 2.8 Hz, 1H), 7.04 (d, J = 8.9 Hz, 1H), 7.66 (d, J = 0.9 Hz, 1H), 7.71 (s, 1H), 7.95 (s, 1H). 1.38 1
    9
    Figure US20160108025A1-20160421-C00088
         		MS (m + 1) = 428.1; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (br. s., 2H), 6.59 (dt, J = 9.1, 3.3 Hz, 1H), 6.62- 6.74 (m, 2H), 7.19 (dd, J = 10.3, 9.1 Hz, 1H), 7.67 (d, J = 0.9 Hz, 1H), 7.74 (s, 1 H), 7.96 (s, 1H). 1.53 3
    10
    Figure US20160108025A1-20160421-C00089
         		MS (m + 1) = 438.1; 1H NMR (400 MHz, DMSO-d6) δ 1.25 (t, J = 7.0 Hz, 3H), 3.98 (q, J = 7.0 Hz, 2H), 4.45 (s, 2H), 6.77 (dd, J = 8.9, 2.7 Hz, 1H), 6.89 (d, J = 2.9 Hz, 1H), 7.02 (d, J = 8.9 Hz, 1H), 7.66 (d, J = 0.9 Hz, 1H), 7.72 (s, 1H), 7.96 (s, 1H). 1.10 5
    11
    Figure US20160108025A1-20160421-C00090
         		MS (m + 1) = 416.3; 1H NMR (400 MHz, DMSO-d6) δ 1.98 (dd, J = 1.5, 0.9 Hz, 3H), 4.38 (d, J = 5.4 Hz, 2H), 4.97 (dd, J = 2.0, 1.0 Hz, 1H), 5.17 (q, J = 1.7 Hz, 1H), 6.52-6.60 (m, 3H), 6.98-7.04 (m, 1H), 7.10 (d, J = 0.9 Hz, 1H), 7.27 (dd, J = 7.9, 1.4 Hz, 1H), 7.59 (d, J = 8.2 Hz, 2H). 1.41 1
    12
    Figure US20160108025A1-20160421-C00091
         		MS (m + 1) = 402.2; 1H NMR (400 MHz, DMSO-d6) δ 0.87 (t, J = 7.3 Hz, 3H), 1.49 (sxt, J = 7.4 Hz, 2H), 2.47 (t, J = 7.9 Hz, 2H), 4.44 (s, 2H), 6.51 (dd, J = 8.3, 2.5 Hz, 2H), 6.62 (d, J = 2.3 Hz, 1H), 7.00 (d, J = 8.3 Hz, 1H), 7.66 (s, 1H), 7.69 (s, 1H), 7.95 (s, 1H). 1.55 1
    13
    Figure US20160108025A1-20160421-C00092
         		MS (m + 1) = 444.2; 1H NMR (400 MHz, DMSO-d6) δ 4.48 (d, J = 3.3 Hz, 2H), 6.62 (dd, J = 8.7, 2.6 Hz, 1 H), 6.75 (dd, J = 2.6, 1.3 Hz, 1H), 6.95 (br. s., 1H), 7.31 (d, J = 8.8 Hz, 1H), 7.68 (d, J = 0.9 Hz, 1H), 7.73 (s, 1H), 7.97 (s, 1H). 1.45 1
    14
    Figure US20160108025A1-20160421-C00093
         		MS (m + 1) = 462.1; 1H NMR (400 MHz, DMSO-d6) δ 4.59 (d, J = 5.6 Hz, 2H), 6.88 (d, J = 8.7 Hz, 1H), 7.23 (d, J = 1.8 Hz, 1H), 7.55 (t, J = 5.8 Hz, 1H), 7.63-7.68 (m, 2H), 7.77 (s, 1H), 7.99 (s, 1H). 1.71 3
    15
    Figure US20160108025A1-20160421-C00094
         		MS (m + 1) = 430.0; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (d, J = 5.3 Hz, 2H), 6.86 (s, 2H), 7.00 (t, J = 5.8 Hz, 1H), 7.68 (d, J = 0.9 Hz, 1H), 7.76 (s, 1H), 7.98 (s, 1H). 1.76 3
    16
    Figure US20160108025A1-20160421-C00095
         		MS (m + 1) = 402.1; 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J = 7.3 Hz, 3H), 1.43-1.56 (m, 2H), 2.47- 2.49 (m, 2H), 4.40 (d, J = 5.2 Hz, 2H), 6.59 (t, J = 6.1 Hz, 1H), 6.79 (dd, J = 8.4, 2.5 Hz, 1H), 6.90 (d, J = 2.5 1.38 1
    Hz, 1H), 7.08 (d, J = 0.9 Hz,
    1H), 7.11 (d, J = 8.5 Hz,
    1H), 7.26 (dd, J = 8.0, 1.4
    Hz, 1H), 7.55-7.62 (m,
    2H).
    17
    Figure US20160108025A1-20160421-C00096
         		MS (m + 1) = 392.3; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (dd, J = 4.2, 1.8 Hz, 2H), 6.60 (dd, J = 8.9, 2.8 Hz, 1H), 6.63-6.71 (m, 1H), 6.74 (d, J = 2.7 Hz, 1H), 6.94 (t, J = 74.3 Hz, 1H), 7.05 (dt, J = 9.0, 0.9 Hz, 1H), 7.14 (d, J = 0.9 Hz, 1H), 7.26 (dd, J = 8.1, 1.3 Hz, 1H), 7.58-7.63 (m, 1.24 1
    2H).
    18
    Figure US20160108025A1-20160421-C00097
         		MS (m + 1) = 452.3; 1H NMR (400 MHz, DMSO-d6) δ 1.20 (d, J = 6.1 Hz, 6 H), 4.45 (s, 2H), 4.50 (quin, J = 6.1 Hz, 1H), 6.37 (br. s., 1 H), 6.77 (dd, J = 8.9, 2.7 Hz, 1H), 6.87 (d, J = 2.8 Hz, 1H), 7.05 (d, J = 8.9 Hz, 1H), 7.65 (s, 1H), 7.73 (s, 1H), 7.95 (s, 1H). 1.45 1
    19
    Figure US20160108025A1-20160421-C00098
         		MS (m + 1) = 394.3; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (d, J = 5.7 Hz, 2H), 6.81-6.87 (m, 2H), 7.00 (dt, J = 6.3, 3.1 Hz, 1H), 7.11 (s, 1H), 7.24 (d, J = 8.0 Hz, 1H), 7.57-7.63 (m, 2H). 1.41 1
    20
    Figure US20160108025A1-20160421-C00099
         		MS (m + 1) = 426.0; 1H NMR (400 MHz, DMSO-d6) δ 4.47 (d, J = 5.8 Hz, 2H), 6.68 (dd, J = 8.7, 2.6 Hz, 1H), 6.89 (d, J = 2.5 Hz, 1H), 7.27-7.32 (m, 2H), 7.38 (t, J = 5.9 Hz, 1H), 7.48 (d, J = 8.7 Hz, 1H), 7.64 (s, 1H), 7.67 (d, J = 8.0 Hz, 1H). 1.32 1
    21
    Figure US20160108025A1-20160421-C00100
         		MS (m + 1) = 390.4; 1H NMR (400 MHz, DMSO-d6) δ 2.13 (s, 3H), 4.30-4.44 (m, 2H), 6.40-6.52 (m, 2H), 6.56 (d, J = 2.8 Hz, 1H), 6.96 (d, J = 8.6 Hz, 1H), 7.08 (s, 1H), 7.25 (d, J = 8.3 Hz, 1H), 7.55-7.62 (m, 2H). 1.34 1
    22
    Figure US20160108025A1-20160421-C00101
         		MS (m + 1) = 492.2; 1H NMR (400 MHz, DMSO-d6) δ 4.48 (br. s., 2H), 4.69 (q, J = 8.9 Hz, 2H), 6.55 (br. s., 1H), 6.80 (dd, J = 8.9, 2.8 Hz, 1H), 6.93 (d, J = 2.8 Hz, 1H), 7.14 (d, J = 9.1 Hz, 1H), 7.65 (s, 1H), 7.73 (s, 1H), 7.96 (s, 1H). 1.40 1
    23
    Figure US20160108025A1-20160421-C00102
         		MS (m + 1) = 444.4; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (d, J = 5.6 Hz, 2H), 6.90 (dd, J = 9.1, 2.9 Hz, 1H), 7.01 (d, J = 2.9 Hz, 1H), 7.05 (t, J = 5.9 Hz, 1H), 7.17 (d, J = 0.9 Hz, 1H), 7.26-7.33 (m, 2H), 7.60-7.65 (m, 2H). 1.40 1
    24
    Figure US20160108025A1-20160421-C00103
         		MS (m + 1) = 460.1; 1H NMR (400 MHz, DMSO-d6) δ 4.53 (d, J = 5.8 Hz, 2H), 6.68 (dd, J = 8.7, 2.5 Hz, 1 H), 6.91 (d, J = 2.6 Hz, 1 H), 7.34 (t, J = 5.8 Hz, 1H), 7.52 (d, J = 8.7 Hz, 1H), 7.66 (s, 1H), 7.75 (s, 1H), 7.98 (s, 1H). 1.76 4
    25
    Figure US20160108025A1-20160421-C00104
         		MS (m + 1) = 460.2; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (br. s., 2H), 6.79- 6.91 (m, 2H), 6.99 (d, J = 2.9 Hz, 1H), 7.14 (d, J = 73.8 Hz, 1H), 7.18 (d, J = 8.9 Hz, 1H), 7.67 (d, J = 0.7 Hz, 1H), 7.73 (s, 1H), 7.97 (s, 1H). 1.36 1
    26
    Figure US20160108025A1-20160421-C00105
         		MS (m + 1) = 406.4; 1H NMR (400 MHz, DMSO-d6) δ 2.34 (s, 3H), 4.43 (d, J = 5.5 Hz, 2H), 6.83 (dd, J = 8.6, 2.6 Hz, 1H), 6.90 (t, J = 6.0 Hz, 1H), 7.00 (d, J = 2.6 Hz, 1H), 7.08 (d, J = 0.9 Hz, 1H), 7.25 (dd, J = 7.9, 1.4 Hz, 1H), 7.36 (d, J = 8.6 Hz, 1H), 7.56-7.62 (m, 2H). 1.30 1
    27
    Figure US20160108025A1-20160421-C00106
         		MS (m + 1) = 458.4; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 4.8 Hz, 2H), 4.66 (q, J = 8.9 Hz, 2H), 6.49 (t, J = 5.9 Hz, 1H), 6.83 (dd, J = 9.0, 2.9 Hz, 1H), 6.91 (d, J = 2.8 Hz, 1H), 7.08-7.14 (m, 2H), 7.26 (dd, J = 7.9, 1.4 Hz, 1H), 7.56-7.61 (m, 2H). 1.32 1
    28
    Figure US20160108025A1-20160421-C00107
         		MS (m + 1) = 338.2; 1H NMR (400 MHz, DMSO-d6) δ 2.36 (s, 3H), 4.37 (d, J = 5.5 Hz, 2H), 6.34-6.43 (m, 3H), 6.51 (t, J = 2.0 Hz, 1H), 6.97 (t, J = 7.9 Hz, 1H), 7.07 (d, J = 1.0 Hz, 1H), 7.25 (dd, J = 8.0, 1.4 1.14 1
    Hz, 1H), 7.55-7.62 (m,
    2H).
    29
    Figure US20160108025A1-20160421-C00108
         		MS (m + 1) = 449.2; 1H NMR (400 MHz, DMSO-d6) δ 4.48 (br. s., 2H), 5.13 (s, 2 H), 6.61 (br. s., 1H), 6.84 (dd, J = 9.1, 2.8 Hz, 1H), 6.95 (d, J = 2.9 Hz, 1H), 7.20 (d, J = 8.9 Hz, 1H), 7.65 (d, J = 0.7 Hz, 1H), 7.74 (s, 1H), 7.96 (s, 1H). 1.24 1
    30
    Figure US20160108025A1-20160421-C00109
         		MS (m + 1) = 388.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 4.61 (d, J = 5.87 Hz, 2 H) 6.80 (d, J = 9.29 Hz, 2H) 7.38 (dd, J = 8.07, 1.22 Hz, 1 H) 7.71 (s, 2H) 7.79 (dd, J = 7.95, 2.32 Hz, 3H) 8.04 (t, J = 6.11 Hz, 1H). 1.17 1
    31
    Figure US20160108025A1-20160421-C00110
         		MS (m + 1) = 436.1; 1H NMR (400 MHz, DMSO-d6) δ 0.89 (t, J = 7.3 Hz, 3H), 1.50 (sxt, J = 7.5 Hz, 2H), 2.53 (br. s., 2H), 4.48 (s, 2 H), 6.67 (br. s., 1H), 6.75 (dd, J = 8.5, 2.3 Hz, 1H), 7.15 (d, J = 8.5 Hz, 1H), 7.67 (d, J = 0.9 Hz, 1H), 7.72 (s, 1H), 7.96 (s, 1H). 1.59 3
    32
    Figure US20160108025A1-20160421-C00111
         		MS (m + 1) = 428.1; 1H NMR (400 MHz, DMSO-d6) δ 4.48 (d, J = 5.3 Hz, 2H), 6.62 (dd, J = 9.0, 2.8 Hz, 1 H), 6.80 (d, J = 2.8 Hz, 1 H), 6.89 (t, J = 6.0 Hz, 1H), 7.24 (dd, J = 9.1, 1.2 Hz, 1 H), 7.65 (s, 1H), 7.73 (s, 1 H), 7.97 (s, 1H). 1.66 4
    33
    Figure US20160108025A1-20160421-C00112
         		MS (m + 1) = 326.1; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (s, 2H), 6.61 (d, J = 8.9 Hz, 2H), 7.06 (d, J = 8.9 Hz, 2H), 7.38 (dd, J = 8.1, 1.3 Hz, 1H), 7.66-7.71 (m, 2H), 7.76 (d, J = 8.0 Hz, 1H). 1.16 1
    34
    Figure US20160108025A1-20160421-C00113
         		MS (m + 1) = 448.2; 1H NMR (400 MHz, DMSO-d6) δ 0.87 (t, J = 7.3 Hz, 3H), 1.48 (sxt, J = 7.5 Hz, 2H), 2.47 (m, 2H), 4.43 (br. s., 2 H), 6.49 (br. s., 1H), 6.55 (dd, J = 8.4, 2.4 Hz, 1H), 6.81 (d, J = 2.5 Hz, 1H), 7.00 (d, J = 8.4 Hz, 1H), 7.65 (s, 1H), 7.69 (s, 1H), 7.95 (s, 1H). 1.57 1
    35
    Figure US20160108025A1-20160421-C00114
         		MS (m + 1) = 407.3; 1H NMR (400 MHz, DMSO-d6) δ 4.36 (d, J = 5.9 Hz, 2H), 6.63 (ddd, J = 13.2, 6.3, 2.8 Hz, 1H), 6.67-6.75 (m, 2H), 7.07 (d, J = 0.9 Hz, 1H), 7.24 ( dd, J = 8.1, 1.3 Hz, 1H), 7.56-7.62 (m, 2H). 1.29 1
    36
    Figure US20160108025A1-20160421-C00115
         		MS (m + 1) = 489.9; 1H NMR (400 MHz, DMSO-d6) δ 4.47 (d, J = 3.9 Hz, 2H), 6.65 (dd, J = 9.0, 2.8 Hz, 1 H), 6.82-6.91 (m, 1H), 6.95 (d, J = 2.8 Hz, 1H), 7.22 (dd, J = 9.0, 1.3 Hz, 1 H), 7.67 (d, J = 0.8 Hz, 1 H), 7.73 (s, 1H), 7.97 (s, 1 H). 1.54 3
    37
    Figure US20160108025A1-20160421-C00116
         		MS (m + 1) = 454.2; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (d, J = 5.8 Hz, 2H), 6.66 (dd, J = 9.0, 2.8 Hz, 1H), 6.83 (t, J = 5.9 Hz, 1H), 6.93 (d, J = 2.7 Hz, 1H), 7.08 (d, J = 0.9 Hz, 1H), 7.17 (dd, J = 9.2, 1.1 Hz, 1H), 7.25 (dd, J = 8.0, 1.3 Hz, 1H), 7.54-7.64 (m, 2H). 1.35 1
    38
    Figure US20160108025A1-20160421-C00117
         		MS (m + 1) = 512.0; 1H NMR (400 MHz, DMSO-d6) δ 4.51 (s, 2H), 6.88 (dd, J = 9.1, 2.8 Hz, 1H), 7.01 (d, J = 2.9 Hz, 1H), 7.30 (d, J = 8.9 Hz, 1H), 7.46 (dd, J = 8.2, 1.0 Hz, 1H), 7.74 (d, J = 7.5 Hz, 1H), 7.79 (s, 1 H). 1.57 3
    39
    Figure US20160108025A1-20160421-C00118
         		MS (m + 1) = 439.2; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.8 Hz, 2H), 6.76 (dd, J = 8.8, 2.8 Hz, 1H), 6.99 (t, J = 5.9 Hz, 1H), 7.06-7.07 (m, 2H), 7.24 (dd, J = 7.9, 1.4 Hz, 1H), 7.45 (d, J = 8.8 Hz, 1H), 7.56-7.62 (m, 2H). 1.35 1
    40
    Figure US20160108025A1-20160421-C00119
         		MS (m + 1) = 372.2; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (s, 2H), 6.36 (dd, J = 8.8, 2.3 Hz, 1H), 6.64 (d, J = 2.3 Hz, 1H), 7.06 (d, J = 8.7 Hz, 1H), 7.40 (dd, J = 8.0, 1.3 Hz, 1H), 7.69- 7.73 (m, 2H), 7.77 (d, J = 1.19 1
    8.1 Hz, 1H).
    41
    Figure US20160108025A1-20160421-C00120
         		MS (m + 1) = 460.4; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.7 Hz, 2H), 6.65 (dd, J = 9.1, 2.7 Hz, 1H), 6.73 (dq, J = 2.8, 1.4 Hz, 1H), 6.97 (t, J = 5.8 Hz, 1H), 7.06 (d, J = 0.9 Hz, 1H), 7.22-7.28 (m, 2H), 7.56-7.62 (m, 2H). 1.41 1
    42
    Figure US20160108025A1-20160421-C00121
         		MS (m + 1) = 414.1; 1H NMR (400 MHz, DMSO-d6) δ 0.86 (t, J = 7.3 Hz, 3H), 1.46 (sxt, J = 7.4 Hz, 2H), 2.43-2.47 (m, 2H), 4.41 (s, 2H), 6.51 (br. s., 1H), 6.56 (dd, J = 8.3, 2.3 Hz, 1 H), 6.79 (d, J = 2.4 Hz, 1 H), 6.97 (d, J = 8.3 Hz, 1 H), 7.38 (dd, J = 8.1, 1.3 Hz, 1H), 7.68 (d, J = 4.4 1.67 4
    Hz, 2H), 7.76 (d, J = 7.8
    Hz, 1H).
    43
    Figure US20160108025A1-20160421-C00122
         		MS (m + 1) = 394.4; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.5 Hz, 2H), 6.48 (ddd, J = 9.1, 2.7, 1.1 Hz, 1H), 6.58 (dd, J = 13.6, 2.7 Hz, 1H), 6.90 (t, J = 5.9 Hz, 1H), 7.17 (td, J = 9.1, 1.2 Hz, 1H), 7.21 (d, J = 0.9 Hz, 1H), 7.28 (dd, J = 8.1, 1.3 Hz, 1H), 7.59-7.67 (m, 2H). 1.32 1
    44
    Figure US20160108025A1-20160421-C00123
         		MS (m + 1) = 424.4; 1H NMR (400 MHz, DMSO-d6) δ 4.36 (s, 2H), 4.58 (q, J = 9.0 Hz, 2H), 6.37 (s, 1H), 6.56 (dd, J = 8.9, 2.8 Hz, 1H), 6.70 (d, J = 2.7 Hz, 1H), 7.00 (d, J = 8.9 Hz, 1H), 7.13 (d, J = 0.9 Hz, 1H), 7.26 (dd, J = 8.0, 1.3 Hz, 1H), 7.57-7.62 (m, 2H). 1.29 1
    45
    Figure US20160108025A1-20160421-C00124
         		MS (m + 1) = 410.2; 1H NMR (400 MHz, DMSO-d6) δ 4.83 (s, 2H), 7.20 (s, 2H), 7.23 (dd, J = 8.01, 1.3 Hz, 1H), 7.36 (s, 1H), 7.57 (s, 1H), 7.68 (d, J = 8.1 Hz, 1H). 1.35 1
    46
    Figure US20160108025A1-20160421-C00125
         		MS (m + 1) = 410.3; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.2 Hz, 2H), 6.63 (dd, J = 9.0, 2.8 Hz, 1H), 6.78 (d, J = 2.8 Hz, 1H), 6.89 (t, J = 6.0 Hz, 1H), 7.20 (dd, J = 9.0, 1.3 Hz, 1H), 7.27-7.33 (m, 2H), 7.64 (s, 1H), 7.66 (d, J = 8.0 Hz, 1H). 1.38 1
    47
    Figure US20160108025A1-20160421-C00126
         		MS (m + 1) = 524.3; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (s, 2H), 6.62-6.68 (m, 1H), 6.92 (d, J = 2.8 Hz, 1H), 7.18 (dd, J = 9.0, 1.3 Hz, 1H), 7.50-7.56 (m, 1H), 7.79-7.85 (m, 2H). 1.47 1
    48
    Figure US20160108025A1-20160421-C00127
         		MS (m + 1) = 455.3; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.5 Hz, 2H), 6.59 (dd, J = 8.9, 2.7 Hz, 1H), 6.72 (dq, J = 2.8, 1.5 Hz, 1H), 6.94 (t, J = 5.9 Hz, 1H), 7.15 (d, J = 0.9 Hz, 1H), 7.26 (dd, J = 8.0, 1.3 Hz, 1H), 7.37 (d, J = 8.8 Hz, 1H), 7.58-7.63 (m, 2H). 1.38 1
    49
    Figure US20160108025A1-20160421-C00128
         		MS (m + 1) = 472.3; 1H NMR (400 MHz, DMSO-d6) δ 1.29 (t, J = 7.0 Hz, 3H), 3.87 (q, J = 7.0 Hz, 2H), 4.41 (d, J = 5.6 Hz, 2H), 6.65-6.71 (m, 3H), 7.41 (dd, J = 8.1, 1.2 Hz, 1H), 7.69 (d, J = 7.5 Hz, 1H), 7.74 (s, 1H). 1.47 1
    50
    Figure US20160108025A1-20160421-C00129
         		MS (m + 1) = 428.2; 1H NMR (400 MHz, DMSO-d6) δ 4.47 (d, J = 5.3 Hz, 2H), 6.47 (dt, J = 9.0, 1.4 Hz, 1 H), 6.60 (dd, J = 13.5, 2.7 Hz, 1H), 6.91 (t, J = 5.7 Hz, 1H), 7.18-7.25 (m, 1H), 7.65 (s, 1H), 7.73 (s, 1H), 7.96 (s, 1H). 1.41 1
    51
    Figure US20160108025A1-20160421-C00130
         		MS (m + 1) = 416.0; 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J = 7.3 Hz, 3H), 1.48 (sxt, J = 7.5 Hz, 2H), 2.47-2.49 (m, 2H), 2.59 (s, 3H), 4.44 (s, 2H), 6.60- 6.72 (m, 1H), 6.77 (dd, J = 8.4, 2.2 Hz, 1H), 6.88 (d, J = 2.3 Hz, 1H), 7.10 (d, J = 8.4 Hz, 1H), 7.36 (d, J = 8.1 Hz, 1H), 7.60 (s, 1H), 7.68 (d, J = 8.1 Hz, 1H). 1.22 5
    52
    Figure US20160108025A1-20160421-C00131
         		MS (m + 1) = 428.4; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (d, J = 5.8 Hz, 2H), 6.90 (dd, J = 8.3, 1.8 Hz, 1H), 7.19 (d, J = 2.4 Hz, 1H), 7.20 (s, 1H), 7.28 (dd, J = 8.1, 1.3 Hz, 1H), 7.56 (t, J = 5.9 Hz, 1H), 7.60-7.67 (m, 3H). 1.36 1
    53
    Figure US20160108025A1-20160421-C00132
         		MS (m + 1) = 468.9; 1H NMR (400 MHz, DMSO-d6) δ 2.57 (s, 3H), 4.43 (d, J = 5.5 Hz, 2H), 6.65 (dd, J = 9.1, 2.8 Hz, 1H), 6.88 (t, J = 5.8 Hz, 1H), 6.91 (d, J = 2.8 Hz, 1H), 7.17 (dd, J = 9.0, 1.3 Hz, 1H), 7.33 (dd, J = 8.0, 1.0 Hz, 1H), 7.59 (s, 1H), 7.65 (d, J = 8.0 Hz, 1H). 1.19 5
    54
    Figure US20160108025A1-20160421-C00133
         		MS (m + 1) = 478.4; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (d, J = 5.8 Hz, 2H), 5.62 (dd, J = 9.1, 2.8 Hz, 1 H), 6.78 (d, J = 2.8 Hz, 1 H), 6.92 (t, J = 5.9 Hz, 1H), 7.20 (dd, J = 9.0, 1.2 Hz, 1 H), 7.41 (dd, J = 8.1, 1.2 Hz, 1H), 7.69 (d, J = 7.3 Hz, 1H), 7.74 (s, 1H). 1.44 1
    55
    Figure US20160108025A1-20160421-C00134
         		MS (m + 1) = 471.4; 1H NMR (400 MHz, DMSO-d6) δ 0.87 (t, J = 1.0 Hz, 3H), 1.23 (s, 2H), 1.49 (sxt, J = 7.5 Hz, 2H), 4.46 (s, 2H), 6.77 (dd, J = 8.4, 2.3 Hz, 1 H), 6.89 (d, J = 2.5 Hz, 1 H), 7.11 (d, J = 8.4 Hz, 1 H), 7.46 (d, J = 8.2 Hz, 1 H), 7.71 (d, J = 7.5 Hz, 1 H), 7.76 (s, 1H). 1.56 1
    56
    Figure US20160108025A1-20160421-C00135
         		MS (m + 1) = 472.0; 1H NMR (400 MHz, DMSO-d6) δ 1.22-1.25 (m, 3H), 3.97 (q, J = 7.0 Hz, 2H), 4.43 (s, 2H), 6.79 (dd, J = 8.9, 2.8 Hz, 1H), 6.88 (d, J = 2.8 Hz, 1H), 6.99 (d, J = 8.9 Hz, 1H), 7.45 (dd, J = 8.3, 1.2 Hz, 1H), 7.70 (d, J = 7.3 Hz, 1H), 7.75 (s, 1H). 1.52 3
    57
    Figure US20160108025A1-20160421-C00136
         		MS (m + 1) = 486.0; 1H NMR (400 MHz, DMSO-d6) δ 1.19 (d, J = 6.0 Hz, 6 H), 4.41 (s, 2H), 4.49 (spt, J = 6.1 Hz, 1H), 6.35 (br. s., 1 H), 6.80 (dd, J = 8.9, 2.8 Hz, 1H), 6.85 (d, J = 2.9 Hz, 1H), 7.02 (d, J = 8.9 Hz, 1H), 7.42 (dd, J = 8.2, 1.2 Hz, 1H), 7.67 (d, J = 7.3 Hz, 1H), 7.74 (s, 1H). 1.55 3
    58
    Figure US20160108025A1-20160421-C00137
         		MS (m + 1) = 392.3; 1H NMR (400 MHz, DMSO-d6) δ 3.52 (q, J = 11.4 Hz, 2H), 4.35 (s, 2H), 6.59 (ddd, J = 8.9, 4.2, 3.0 Hz, 1H), 6.66 (dd, J = 6.3, 2.9 Hz, 1H), 6.94 (t, J = 9.1 Hz, 1H), 7.13 (d, J = 0.9 Hz, 1H), 7.27 (dd, J = 7.9, 1.4 Hz, 1H), 7.55-7.62 (m, 2H). 1.23 1
    59
    Figure US20160108025A1-20160421-C00138
         		MS (m + 1) = 371.2; 1H NMR (400 MHz, DMSO-d6) δ 4.38 (d, J = 5.8 Hz, 2H), 6.58-6.66 (m, 3H), 6.78 (t, J = 2.0 Hz, 1H), 6.98 (t, J = 8.0 Hz, 1H), 7.08 (d, J = 1.0 Hz, 1H), 7.25 (dd, J = 8.1, 1.2 Hz, 1H), 7.54- 7.62 (m, 2H). 1.22 1
    60
    Figure US20160108025A1-20160421-C00139
         		MS (m + 1) = 494.4; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (s, 2H), 6.81-6.88 (m, 1H), 6.96 (d, J = 2.91 Hz, 1H), 7.12 (d, J = 74.0 Hz, 1H), 7.14 (d, J = 8.84 Hz, 1H), 7.53 (dd, J = 8.27, 1.20 Hz, 1H), 7.78-7.85 (m, 2H). 1.35 1
    61
    Figure US20160108025A1-20160421-C00140
         		MS (m + 1) = 461.9; 1H NMR (400 MHz, DMSO-d6) δ 4.53 (d, J = 4.8 Hz, 2H), 6.65 (dd, J = 8.8, 1.8 Hz, 1 H), 6.83 (d, J = 2.1 Hz, 1 H), 7.36-7.42 (m, 1H), 7.45 (d, J = 8.8 Hz, 2H), 7.75 (d, J = 6.5 Hz, 1H), 7.78 (s, 1H). 1.53 1
    62
    Figure US20160108025A1-20160421-C00141
         		MS (m + 1) = 382.4; 1H NMR (400 MHz, DMSO-d6) δ 3.51 (s, 3H), 3.66 (s, 6H), 4.44 (s, 2H), 6.00 (s, 2H), 7.42 (dd, J = 8.1, 1.3 Hz, 1H), 7.71 (d, J = 1.0 Hz, 1H), 7.74 (s, 1H), 7.77 (d, J = 8.1 Hz, 1H). 0.92 1
    63
    Figure US20160108025A1-20160421-C00142
         		MS (m + 1) = 376.3; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (s, 2H), 6.59 (br. s., 1H), 6.62-6.68 (m, 2H), 7.03 (d, J = 8.3 Hz, 2H), 7.14 (d, J = 0.7 Hz, 1H), 7.27 (dd, J = 8.1, 1.1 Hz, 1H), 7.56- 7.63 (m, 2H). 1.27 1
    64
    Figure US20160108025A1-20160421-C00143
         		MS (m + 1) = 425.1; 1H NMR (400 MHz, DMSO-d6) δ 4.47 (d, J = 5.6 Hz, 2H), 6.67 (dd, J = 8.7, 2.6 Hz, 1 H), 6.87 (d, J = 2.5 Hz, 1 H), 7.39 (t, J = 5.8 Hz, 1H), 7.45-7.50 (m, 2H), 7.72 (s, 1H), 7.75 (s, 1H), 7.78 (d, J = 1.1 Hz, 1H). 1.11 5
    65
    Figure US20160108025A1-20160421-C00144
         		MS (m + 1) = 409.9; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (d, J = 3.8 Hz, 2H), 6.61 (dd, J = 9.1, 2.8 Hz, 1 H), 6.76 (d, J = 2.8 Hz, 1 H), 6.90 (br. s., 1H), 7.16- 7.23 (m, 1H), 7.47 (dd, J = 8.6, 1.7 Hz, 1H), 7.74 (s, 2 H), 7.78 (d, J = 1.2 Hz, 1 H). 1.07 5
    66
    Figure US20160108025A1-20160421-C00145
         		MS (m + 1) = 402.1; 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J = 7.3 Hz, 3H), 1.49 (sxt, J = 7.5 Hz, 2H), 2.53 (m, 2H), 4.41 (s, 2H), 6.63 (br. s., 1H), 6.77 (dd, J = 8.4, 2.3 Hz, 1H), 6.88 (d, J = 2.6 Hz, 1H), 7.11 (d, J = 8.4 Hz, 1H), 7.48 (dd, J = 1.11 5
    8.7, 1.7 Hz, 1H), 7.69-
    7.74 (m, 2H), 7.78 (d, J =
    1.1 Hz, 1H).
    67
    Figure US20160108025A1-20160421-C00146
         		MS (m + 1) = 372.0: 1H NMR (400 MHz, DMSO-d6) δ 4.37 (s, 2H) 6.35 (dd, J = 8.8, 2.3 Hz, 1H), 6.62 (d, J = 2.3 Hz, 1H), 7.06 (d, J = 8.8 Hz, 1H), 7.48 (dd, J = 8.7, 1.7 Hz, 1H), 7.67- 7.74 (m, 2H), 7.78 (d, J = 1.0 Hz, 1H). 1.00 5
    68
    Figure US20160108025A1-20160421-C00147
         		MS (m + 1) = 368.0: 1H NMR (400 MHz, METHANOL-d4) δ 0.90 (t, J = 7.4 Hz, 3H) 1.50-1.63 (m, 2H) 2.56 (dd, J = 8.3, 6.9 Hz, 2H) 4.39 (s, 2H) 6.47 (dd, J = 8.6, 2.9 Hz, 1H) 6.55 (d, J = 2.8 Hz, 1H) 7.01 (d, J = 8.7 Hz, 1H) 7.26 (d, J = 1.0 Hz, 1H) 7.35 (dd, J = 8.5, 1.8 Hz, 1H) 7.53 (d, J = 8.6 Hz, 1H) 7.64 (d, J = 1.1 Hz, 1H). 1.09 5
    69
    Figure US20160108025A1-20160421-C00148
         		MS (m + 1) = 382.0; 1H NMR (400 MHz, DMSO-d6) δ 0.91 (t, J = 7.3 Hz, 3H), 1.33-1.46 (m, 2H), 2.17 (s, 3H), 2.46-2.48 (m, 2 H), 4.35 (s, 2H), 6.41-6.47 (m, 2H), 7.46 (dd, J = 8.7, 1.7 Hz, 1H), 7.69-7.73 (m, 2H), 7.76 (d, J = 1.1 Hz, 1 H). 1.13 5
    70
    Figure US20160108025A1-20160421-C00149
         		MS (m + 1) = 440.1; 1H NMR (400 MHz, DMSO-d6) δ 2.63 (s, 3H), 4.47 (d, J = 5.6 Hz, 2H), 6.68 (dd, J = 8.7, 2.5 Hz, 1H), 6.89 (d, J = 2.6 Hz, 1H), 7.35 (t, J = 5.8 Hz, 1H), 7.45-7.51 (m, 2H), 7.67 (d, J = 8.6 Hz, 1 H), 7.79 (d, J = 1.0 Hz, 1 H). 1.11 5
    71
    Figure US20160108025A1-20160421-C00150
         		MS (m + 1) = 368.0; 1H NMR (400 MHz, DMSO-d6) δ 0.86 (t, J = 7.3 Hz, 3H), 1.48 (sxt, J = 7.4 Hz, 2H), 2.45 (t, J = 7.8 Hz, 2H), 4.37 (s, 2H), 6.52 (dd, J = 8.3, 2.5 Hz, 1H), 6.60 (d, J = 2.5 Hz, 1H), 6.97 (d, J = 8.4 Hz, 1H), 7.47 (dd, J = 1.07 5
    8.7, 1.7 Hz, 1H), 7.71 (t, J =
    4.2 Hz, 2H), 7.77 (d, J =
    1.0 Hz, 1H).
    72
    Figure US20160108025A1-20160421-C00151
         		MS (m + 1) = 394.0; 1H NMR (400 MHz, DMSO-d6) δ 4.38 (s, 2H), 6.56-6.69 (m, 3H), 7.16 (dd, J = 10.4, 9.1 Hz, 1H), 7.47 (dd, J = 8.5, 1.5 Hz, 1H), 7.69- 7.74 (m, 2H), 7.78 (d, J = 1.2 Hz, 1H). 1.03 5
    73
    Figure US20160108025A1-20160421-C00152
         		MS (m + 1) = 410.2; 1H NMR (400 MHz, DMSO-d6) δ 1.46 (d, J = 6.6 Hz, 3H), 4.65 (quin, J = 6.8 Hz, 1H), 6.73 (s, 2H), 6.99 (d, J = 7.0 Hz, 1H) 7.33-7.39 (m, 2H) 7.62 (d, J = 8.6 Hz, 1 H) 7.68 (d, J = 1.5 Hz, 1H). 1.40 1
    74
    Figure US20160108025A1-20160421-C00153
         		MS (m + 1) = 439.9; 1H NMR (400 MHz, DMSO-d6) δ 1.49 (d, J = 6.7 Hz, 3H), 4.71 (quin, J = 6.8 Hz, 1H), 6.57 (dd, J = 8.7, 2.3 Hz, 1 H), 6.79 (d, J = 2.2 Hz, 1 H), 7.32 (d, J = 6.9 Hz, 1 H), 7.39-7.45 (m, 2H), 7.49 (s, 1H), 7.66 (d, J = 8.6 Hz, 1H), 7.73 (d, J = 1.5 Hz, 1H). 1.11 5
    75
    Figure US20160108025A1-20160421-C00154
         		MS (m + 1) = 409.9; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (d, J = 5.6 Hz, 2H), 6.52 (d, J = 8.2 Hz, 2H), 6.65 (t, J = 1.9 Hz, 1H), 7.04 (t, J = 5.8 Hz, 1H), 7.33-7.37 (m, 2H), 7.64 (d, J = 8.4 Hz, 1H), 7.68 (s, 1H). 1.19 5
    76
    Figure US20160108025A1-20160421-C00155
         		MS (m + 1) = 418.0; 1H NMR (400 MHz, DMSO-d6) δ 0.85 (t, J = 7.3 Hz, 3H), 1.46 (sxt, J = 7.4 Hz, 2H), 2.36-2.43 (m, 2H), 4.37 (s, 2H), 6.48-6.57 (m, 2 H), 7.02 (d, J = 8.3 Hz, 1 H), 7.47 (dd, J = 8.6, 1.5 Hz, 1H), 7.68-7.74 (m, 2 H), 7.77 (s, 1H). 1.18 5
    77
    Figure US20160108025A1-20160421-C00156
         		MS (m + 1) = 425.0; 1H NMR (400 MHz, DMSO-d6) δ 1.47 (d, J = 6.7 Hz, 3H), 4.64 (quin, J = 6.7 Hz, 1H), 6.52 (dd, J = 9.1, 2.8 Hz, 1 H), 6.67 (d, J = 2.7 Hz, 1 H), 6.85 (d, J = 6.9 Hz, 1 H), 7.14 (dd, J = 9.1, 1.2 Hz, 1H), 7.48 (dd, J = 8.7, 1.7 Hz, 1H), 7.64 (s, 1H), 7.69 (d, J = 8.6 Hz, 1H), 7.77 (d, J = 1.5 Hz, 1H). 1.09 5
    78
    Figure US20160108025A1-20160421-C00157
         		MS (m + 1) = 388.0; 1H NMR (400 MHz, DMSO-d6) δ 1.17 (t, J = 7.5 Hz, 3H), 2.74 (q, J = 7.5 Hz, 2H), 5.08 (br. s., 2H), 7.30 (dd, J = 8.4, 1.6 Hz, 1 H,) 7.39 (d, J = 7.8 Hz, 1H), 7.51 (d, J = 8.2 Hz, 1H), 7.58 (s, 1 H), 7.66 (s, 1H), 7.68-7.74 1.10 5
    (m, 2H).
    79
    Figure US20160108025A1-20160421-C00158
         		MS (m + 1) = 352.1; 1H NMR (400 MHz, DMSO-d6) δ 0.84 (t, J = 7.3 Hz, 3H), 1.46 (sxt, J = 7.4 Hz, 2H), 2.37 (t, J = 7.5 Hz, 2H), 4.36 (s, 2H), 6.31 (dd, J = 13.1, 2.3 Hz, 1H), 6.37 (dd, J = 8.3, 2.3 Hz, 1H), 6.90 (t, J = 8.7 Hz, 1H), 7.47 (dd, J = 8.7, 1.7 Hz, 1H), 7.67-7.74 (m, 2H), 7.77 1.07 5
    (d, J = 1.0 Hz, 1H).
    80
    Figure US20160108025A1-20160421-C00159
         		MS (m + 1) = 348.1; 1H NMR (400 MHz, DMSO-d6) δ 0.87 (t, J = 7.3 Hz, 3H), 1.43 (sxt, J = 7.5 Hz, 2H), 2.11 (s, 3H), 2.32-2.39 (m, 2H), 4.34 (s, 2H), 6.35 (dd, J = 8.2, 2.5 Hz, 1H), 6.43 (d, J = 2.2 Hz, 1H), 6.78 (d, J = 8.2 Hz, 1H), 7.46 (dd, J = 8.7, 1.7 Hz, 1 H), 7.66-7.71 (m, 2H), 1.06 5
    7.76 (d, J = 1.0 Hz, 1H).
    81
    Figure US20160108025A1-20160421-C00160
         		MS (m + 1) = 416.4; 1H NMR (400 MHz, DMSO-d6) δ 0.85 (t, J = 7.3 Hz, 3H), 1.39-1.51 (m, 5 H), 2.41- 2.48 (m, 2H), 4.57 (quin, J = 6.6 Hz, 1H), 6.52 (d, J = 6.7 Hz, 1H), 6.65 (dd, J = 8.5, 2.1 Hz, 1H), 6.86 (d, J = 2.5 Hz, 1H), 7.03 (d, J = 8.3 Hz, 1H), 7.05 (d, J = 0.9 Hz, 1H), 7.29 (dd, J = 8.4, 1.7 Hz, 1H), 7.53 (d, J = 8.4 Hz, 1H), 7.61 (d, J = 1.46 1
    1.5 Hz, 1H).
    82
    Figure US20160108025A1-20160421-C00161
         		MS (m + 1) = 416.0; 1H NMR (400 MHz, DMSO-d6) δ 0.87 (t, J = 7.3 Hz, 3H), 1.44-1.62 (m, 2H), 2.56 (s, 3H), 2.68 (br. s., 2H), 5.09 (s, 2H), 7.27-7.34 (m, 1H), 7.39 (d, J = 8.4 Hz, 1H), 7.47 (s, 1H), 7.56 (d, J = 4.0 Hz, 2H), 7.64 (d, J = 8.6 Hz, 1H). 1.13 5
    83
    Figure US20160108025A1-20160421-C00162
         		MS (m + 1) = 385.9; 1H NMR (400 MHz, DMSO-d6) δ 1.46 (d, J = 6.7 Hz, 3H), 4.60 (br. s., 1H), 6.26 (dd, J = 8.8, 2.3 Hz, 1H), 6.52 (d, J = 2.2 Hz, 2H), 6.99 (d, J = 8.8 Hz, 1H), 7.49 (dd, J = 8.8, 1.7 Hz, 1H), 7.69 (t, J = 4.2 Hz, 2H), 7.78 (d, J = 1.01 5
    1.5 Hz, 1H).
    84
    Figure US20160108025A1-20160421-C00163
         		MS (m + 1) = 382.3; 1H NMR (400 MHz, DMSO-d6) δ 0.83 (t, J = 7.3 Hz, 3H), 1.37-1.48 (m, 5 H), 2.38- 2.44 (m, 2H), 4.58 (br. s., 1 H), 6.35-6.45 (m, 2H), 6.52 (d, J = 2.3 Hz, 1H), 6.89 (d, J = 8.4 Hz, 1H), 7.49 (dd, J = 8.7, 1.7 Hz, 1 H), 7.66-7.71 (m, 2H), 7.78 (d, J = 1.5 Hz, 1H). 1.44 1
    85
    Figure US20160108025A1-20160421-C00164
         		MS (m + 1) = 504.5; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 5.9 Hz, 2H), 6.98 (s, 2H), 6.98-7.02 (m, 1H), 7.34 (dd, J = 8.2, 1.3 Hz, 1H), 7.63-7.64 (m, 1H), 7.64-7.66 (m, 1H), 7.75 (d, J = 8.1 Hz, 1H), 13.51 (br. s., 1H). 1.21 8
    86
    Figure US20160108025A1-20160421-C00165
         		MS (m + 1) = 371.6; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (d, J = 6.0 Hz, 2H), 6.82 (s, 2H), 7.05 (t, J = 6.1 Hz, 1H), 7.34 (dd, J = 8.1, 1.4 Hz, 1H), 7.62-7.65 (m, 1H), 7.65 (s, 1H), 7.75 (d, J = 8.1 Hz, 1H), 13.51 (br. s, 1H). 1.19 8
    87
    Figure US20160108025A1-20160421-C00166
         		MS (m + 1) = 402.1; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (d, J = 5.8 Hz, 2H), 6.66 (dd, J = 8.7, 2.5 Hz, 1H), 6.86 (d, J = 2.5 Hz, 1H), 7.08 (s, 1H), 7.23 (dd, J = 7.9, 1.4 Hz, 1H), 7.35 (t, J = 5.9 Hz, 1H), 7.47 (d, J = 8.6 Hz, 1H), 7.53 (s, 1H), 7.60 (d, J = 8.0 Hz, 1H). 1.36 1
    88
    Figure US20160108025A1-20160421-C00167
         		MS (m + 1) = 386.0; 1H NMR (400 MHz, DMSO-d6) δ 4.38 (d, J = 5.9 Hz, 2H), 6.61 (dd, J = 9.0, 2.8 Hz, 1H), 6.75 (d, J = 2.8 Hz, 1H), 6.85 (t, J = 5.9 Hz, 1H), 7.02 (s, 1H), 7.19 (dq, J = 9.0, 1.3 Hz, 1H), 7.22 (dd, J = 8.0, 1.4 Hz, 1H), 7.51 (s, 1H), 7.58 (d, J = 8.0 Hz, 1H). 1.17 6
    89
    Figure US20160108025A1-20160421-C00168
         		MS (m + 1) = 348.0; 1H NMR (400 MHz, DMSO-d6) δ 4.33 (d, J = 5.9 Hz, 2H), 6.34 (dd, J = 8.8, 2.3 Hz, 1H), 6.50 (t, J = 6.0 Hz, 1H), 6.62 (d, J = 2.3 Hz, 1H), 6.88 (d, J = 1.0 Hz, 1H), 7.04 (d, J = 8.7 Hz, 1.22 1
    1H), 7.20 (dd, J = 7.9, 1.4
    Hz, 1H), 7.48 (s, 1H), 7.53
    (d, J = 8.0 Hz, 1H).
    90
    Figure US20160108025A1-20160421-C00169
         		MS (m + 1) = 431.2; 1H NMR (400 MHz, DMSO-d6) δ 4.38 (d, J = 5.4 Hz, 2H), 6.65 (dd, J = 9.1, 2.8 Hz, 1H), 6.87 (t, J = 5.9 Hz, 1H), 6.91 (d, J = 2.7 Hz, 1H), 7.02 (d, J = 4.2 Hz, 1H), 7.14-7.20 (m, 1H), 7.22 (dd, J = 8.0, 1.4 Hz, 1H), 7.52 (s, 1H), 7.58 (d, J = 8.0 Hz, 1H). 1.38 1
    91
    Figure US20160108025A1-20160421-C00170
         		MS (m + 1) = 436.2; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (d, J = 5.8 Hz, 2H), 6.88 (dd, J = 8.8, 2.6 Hz, 1H), 7.14 (s, 1H), 7.16 (d, J = 2.7 Hz, 1H), 7.26 (dd, J = 8.0, 1.4 Hz, 1H), 7.54- 7.60 (m, 3H), 7.62 (d, J = 8.0 Hz, 1H). 1.39 1
    92
    Figure US20160108025A1-20160421-C00171
         		MS (m + 1) = 420.4; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.6 Hz, 2H), 6.87 (dd, J = 9.0, 3.1 Hz, 1H), 6.93 (d, J = 3.4 Hz, 1H), 6.99 (d, J = 3.0 Hz, 1H), 7.03 (t, J = 5.9 Hz, 1H), 7.18-7.25 (m, 1H), 7.29 (d, J = 9.0 Hz, 1H), 7.50 (d, J = 3.2 Hz, 1H), 7.56 (dd, J = 8.0, 3.7 Hz, 1H). 1.38 1
    93
    Figure US20160108025A1-20160421-C00172
         		MS (m + 1) = 344.2; 1H NMR (400 MHz, DMSO-d6) δ 0.86 (t, J = 7.3 Hz, 3H), 1.42-1.53 (m, 2H), 2.43- 2.46 (m, 2H), 4.37 (d, J = 5.7 Hz, 2H), 6.45 (t, J = 6.2 Hz, 1H), 6.51 (dd, J = 8.3, 2.4 Hz, 1H), 6.59 (d, J = 2.4 Hz, 1H), 6.96 (d, J = 8.3 Hz, 1H), 7.31 (dd, J = 7.9, 1.4 1.41 1
    Hz, 1H), 7.42 (s, 1H), 7.59
    (s, 1H), 7.67 (d, J = 8.1 Hz,
    1H).
    94
    Figure US20160108025A1-20160421-C00173
         		MS (m + 1) = 398.3; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.9 Hz, 2H), 6.50 (d, J = 2.6 Hz, 1H), 6.54 (dd, J = 9.0, 2.6 Hz, 1H), 6.76 (t, J = 6.1 Hz, 1H), 7.11 (d, J = 9.0 Hz, 1H), 7.32 (dd, J = 8.1, 1.3 Hz, 1H), 7.48 (s, 1H), 7.62 (s, 1H), 7.70 (d, J = 8.1 Hz, 1H). 1.35 1
    95
    Figure US20160108025A1-20160421-C00174
         		MS (m + 1) = 378.2; 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J = 7.3 Hz, 3H), 1.42-1.56 (m, 2H), 2.46- 2.49 (m, 2H), 4.37 (d, J = 5.9 Hz, 2H), 6.57 (t, J = 6.0 Hz, 1H), 6.77 (dd, J = 8.4, 2.5 Hz, 1H), 6.88 (d, J = 2.6 Hz, 1H), 6.89 (d, J = 1.0 Hz, 1.49 1
    1H), 7.10 (d, J = 8.4 Hz,
    1H), 7.21 (dd, J = 8.0, 1.4
    Hz, 1H), 7.47 (s, 1H), 7.53
    (d, J = 8.0 Hz, 1H).
    96
    Figure US20160108025A1-20160421-C00175
         		MS (m + 1) = 382.4; 1H NMR (600 MHz, DMSO-d6) δ 2.34 (s, 3H), 4.42 (d, J = 5.4 Hz, 2H), 6.81 (dd, J = 8.7, 2.6 Hz, 1H), 6.92 (t, J = 6.0 Hz, 1H), 6.98 (d, J = 2.6 Hz, 1H), 7.04 (s, 1H), 7.23 (dd, J = 8.0, 1.4 Hz, 1H), 7.35 (d, J = 8.6 Hz, 1H), 7.52 (s, 1H), 7.58 (d, J = 8.0 Hz, 1H). 1.31 1
    97
    Figure US20160108025A1-20160421-C00176
         		MS (m + 1) = 314.1; 1H NMR (400 MHz, DMSO-d6) δ 2.35 (s, 3H), 4.34 (d, J = 5.9 Hz, 2H), 6.34 (t, J = 6.1 Hz, 1H), 6.37-6.39 (m, 1H), 6.39-6.41 (m, 1H), 6.48 (t, J = 2.0 Hz, 1H), 6.86 (s, 1H), 6.96 (t, J = 7.9 Hz, 1H), 7.19 (dd, J = 8.1, 1.4 1.15 1
    Hz, 1H), 7.46 (s, 1H), 7.51
    (d, J = 8.0 Hz, 1H).
    98
    Figure US20160108025A1-20160421-C00177
         		MS (m + 1) = 432.2; 1H NMR (400 MHz, DMSO-d6) δ 2.73-2.80 (m, 4H), 3.63- 3.71 (m, 4H), 4.34 (d, J = 5.4 Hz, 2H), 6.36 (t, J = 5.7 Hz, 1H), 6.58 (dd, J = 8.7, 2.6 Hz, 1H), 6.85 (d, J = 2.6 Hz, 1H), 6.93 (d, J = 8.7 Hz, 1H), 7.18 (s, 1H), 7.25 (dd, J = 8.1, 1.4 Hz, 1H), 7.53 (s, 1H), 7.60 (d, J = 8.0 Hz, 1H). 1.14 1
    99
    Figure US20160108025A1-20160421-C00178
         		MS (m + 1) = 393.7; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 5.9 Hz, 2H), 6.65 (d, J = 8.8 Hz, 2H), 7.02 (br. s, 1H), 7.19-7.21 (m, 1H), 7.47-7.54 (m, 3H), 7.57 (d, J = 8.0 Hz, 1H), 7.63-7.68 (m, 1H), 7.79-7.86 (m, 1H). 1.27 1
    100
    Figure US20160108025A1-20160421-C00179
         		MS (m + 1) = 364.1; 1H NMR (400 MHz, DMSO-d6) δ 1.09 (t, J = 7.4 Hz, 3H), 2.55 (q, J = 7.5 Hz, 2H), 4.38 (d, J = 5.6 Hz, 2H), 6.59 (t, J = 6.1 Hz, 1H), 6.78 (dd, J = 8.4, 2.5 Hz, 1H), 6.88 (d, J = 2.5 Hz, 1H), 6.97 (s, 1H), 7.11 (d, J = 8.4 Hz, 1H), 7.22 (dd, J = 8.0, 1.4 Hz, 1H), 7.50 (s, 1H), 7.55 (d, J = 8.0 Hz, 1H). 1.34 1
    101
    Figure US20160108025A1-20160421-C00180
         		MS (m + 1) = 404.4; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (d, J = 5.7 Hz, 2H), 6.87 (d, J = 8.5 Hz, 1H), 7.04 (s, 1H), 7.17 (d, J = 2.5 Hz, 1H), 7.23 (dd, J = 8.1, 1.4 Hz, 1H), 7.54 (s, 1H), 7.56-7.64 (m, 3H). 1.38 1
    102
    Figure US20160108025A1-20160421-C00181
         		MS (m + 1) = 366.3; 1H NMR (400 MHz, DMSO-d6) δ 2.12 (s, 3H), 4.35 (d, J = 5.8 Hz, 2H), 6.42-6.51 (m, 2H), 6.54 (d, J = 2.8 Hz, 1H), 6.91-6.99 (m, 2H), 7.21 (dd, J = 7.9, 1.4 Hz, 1H), 7.49 (s, 1H), 7.54 (d, J = 8.0 Hz, 1H). 1.36 1
    103
    Figure US20160108025A1-20160421-C00182
         		MS (m + 1) = 364.2; 1H NMR (400 MHz, DMSO-d6) δ ppm 4.53 (d, J = 5.99 Hz, 2 H) 6.78 (d, J = 9.05 Hz, 2H) 6.86 (d, J = 0.86 Hz, 1H) 7.18 (dd, J = 8.07, 1.34 Hz, 1 H) 7.49 (s, 1H) 7.54 (d, J = 8.07 Hz, 1H) 7.77 (d, J = 8.19 Hz, 2H) 8.02 (t, J = 5.99 Hz, 1H). 1.25 1
    104
    Figure US20160108025A1-20160421-C00183
         		MS (m + 1) = 436.4; 1H NMR (600 MHz, DMSO-d6) δ 4.39 (d, J = 5.6 Hz, 2H), 6.62 (dd, J = 9.1, 2.7 Hz, 1H), 6.71 (dq, J = 2.8, 1.4 Hz, 1H), 6.97 (t, J = 5.9 Hz, 1H), 7.08 (s, 1H), 7.24 (ddd, J = 8.8, 2.9, 1.5 Hz, 2H), 7.53 (s, 1H), 7.60 (d, J = 8.0 Hz, 1H). 1.42 1
    105
    Figure US20160108025A1-20160421-C00184
         		MS (m + 1) = 326.2; 1H NMR (400 MHz, DMSO-d6) δ 4.03-4.08 (m, 2H), 4.08- 4.14 (m, 2H), 4.29 (s, 2H), 6.06 (d, J = 2.6 Hz, 1H), 6.12 (dd, J = 8.7, 2.6 Hz, 1H), 6.54 (d, J = 8.7 Hz, 1H), 7.22-7.32 (m, 2H), 7.54 (s, 1H), 7.61 (d, J = 8.0 0.95 1
    Hz, 1H).
    106
    Figure US20160108025A1-20160421-C00185
         		MS (m + 1) = 383.3; 1H NMR (400 MHz, DMSO-d6) δ 4.34 (d, J = 5.9 Hz, 2H), 6.60 (ddd, J = 13.2, 6.3, 2.7 Hz, 1H), 6.64-6.68 (m, 1H), 6.71 (t, J = 5.9 Hz, 1H), 6.95 (s, 1H), 7.20 (dd, J = 8.0, 1.4 Hz, 1H), 7.50 (s, 1H), 7.56 (d, J = 8.0 Hz, 1H). 1.30 1
    107
    Figure US20160108025A1-20160421-C00186
         		MS (m + 1) = 500.3; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.9 Hz, 2H), 6.63 (dd, J = 9.0, 2.8 Hz, 1 H), 6.87 (t, J = 5.9 Hz, 1H), 6.90 (d, J = 2.7 Hz, 1H), 7.17 (dd, J = 9.0, 1.2 Hz, 1 H), 7.37 (d, J = 8.4 Hz, 1 H), 7.61-7.67 (m, 2H). 1.50 1
    108
    Figure US20160108025A1-20160421-C00187
         		MS (m + 1) = 400.3; 1H NMR (400 MHz, DMSO-d6) δ 4.33 (d, J = 5.7 Hz, 2H), 4.58 (q, J = 8.9 Hz, 2H), 6.35 (t, J = 6.1 Hz, 1H), 6.54 (dd, J = 8.9, 2.8 Hz, 1H), 6.68 (d, J = 2.7 Hz, 1H), 6.88 (d, J = 1.0 Hz, 1H), 6.99 (d, J = 8.9 Hz, 1H), 7.19 (dd, J = 8.1, 1.4 1.30 1
    Hz, 1H), 7.47 (s, 1H), 7.52
    (d, J = 8.0 Hz, 1H).
    109
    Figure US20160108025A1-20160421-C00188
         		MS (m + 1) = 353.1; 1H NMR (400 MHz, DMSO-d6) δ 2.94-3.02 (m, 4H), 3.64- 3.73 (m, 4H), 4.32 (d, J = 6.0 Hz, 2H), 6.07 (t, J = 6.6 Hz, 1H), 6.08-6.15 (m, 2H), 6.20 (t, J = 2.3 Hz, 1H), 6.82 (d, J = 1.0 Hz, 1H), 6.87 (t, J = 8.0 Hz, 0.95 1
    1H), 7.18 (dd, J = 8.0, 1.4
    Hz, 1H), 7.45 (s, 1H), 7.49
    (d, J = 8.0 Hz, 1H).
    110
    Figure US20160108025A1-20160421-C00189
         		MS (m + 1) = 388.1; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.8 Hz, 2H), 6.89 (dd, J = 5.3, 2.9 Hz, 1H), 6.95 (t, J = 6.0 Hz, 1H), 6.98 (dd, J = 5.9, 2.9 Hz, 1H), 7.09 (s, 1H), 7.24 (dd, J = 8.0, 1.4 Hz, 1H), 7.55 (s, 1H), 7.61 (d, J = 8.0 Hz, 1H). 1.32 1
    111
    Figure US20160108025A1-20160421-C00190
         		MS (m + 1) = 445.9; 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J = 7.3 Hz, 3H), 1.48 (sxt, J = 7.5 Hz, 2H), 2.48 (br. s., 2H), 4.42 (d, J = 4.7 Hz, 2H), 6.64 (t, J = 5.4 Hz, 1H), 6.75 (dd, J = 8.4, 2.3 Hz, 1H), 6.87 (d, J = 2.5 Hz, 1H), 7.10 (d, J = 8.4 Hz, 1H), 7.38 (d, J = 8.8 Hz, 1H), 7.60-7.66 (m, 2H). 1.78 4
    112
    Figure US20160108025A1-20160421-C00191
         		MS (m + 1) = 337.1; 1H NMR (400 MHz, DMSO-d6) δ 4.62 (d, J = 5.9 Hz, 2H), 6.65 (d, J = 8.9 Hz, 1H), 6.88 (s, 1H), 7.17 (dd, J = 7.9, 1.4 Hz, 1H), 7.45 (s, 1H), 7.52 (d, J = 8.0 Hz, 1H), 7.64 (dd, J = 8.9, 2.5 Hz, 1H), 7.87 (t, J = 5.9 Hz, 1H), 8.30 (s, 1H). 0.87 6
    113
    Figure US20160108025A1-20160421-C00192
         		MS (m − 1) = 366.2; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.9 Hz, 2H), 6.68 (d, J = 9.0 Hz, 2H), 6.94 (s, 1H), 7.04 (t, J = 6.0 Hz, 1H), 7.20 (dd, J = 8.0, 1.4 Hz, 1H), 7.33 (d, J = 8.6 Hz, 2H), 7.49 (s, 1H), 7.55 (d, J = 8.0 Hz, 1H). 1.40 1
    114
    Figure US20160108025A1-20160421-C00193
         		MS (m + 1) = 339.3; 1H NMR (400 MHz, DMSO-d6) δ 2.67 (s, 3H), 4.42 (d, J = 5.7 Hz, 2H), 6.49 (t, J = 6.1 Hz, 1H), 6.81 (dd, J = 8.7, 2.3 Hz, 1H), 6.94 (s, 1H), 6.97 (d, J = 2.2 Hz, 1H), 7.25 (dd, J = 7.9, 1.4 Hz, 1H), 7.50-7.57 (m, 2H), 7.60 1.01 1
    (d, J = 8.6 Hz, 1H).
    115
    Figure US20160108025A1-20160421-C00194
         		MS (m + 1) = 332.1; H NMR (400 MHz, DMSO-d6) δ 3.68 (s, 3H), 4.30 (d, J = 5.8 Hz, 2H), 6.12 (t, J = 6.2 Hz, 1H), 6.53 (dd, J = 8.9, 2.8 Hz, 1H), 6.67 (d, J = 2.7 Hz, 1H), 6.87 (d, J = 8.9 Hz, 2H), 7.18 (dd, J = 8.0, 1.4 Hz, 1H), 7.46 (s, 1H), 7.51 (d, J = 8.0 Hz, 1H). 1.09 1
    116
    Figure US20160108025A1-20160421-C00195
         		MS (m − 1) = 402.0; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (d, J = 5.8 Hz, 2H), 7.04 (s, 1H), 7.07 (s, 1H), 7.16 (s, 2H), 7.25 (dd, J = 8.1, 1.4 Hz, 1H), 7.31 (t, J = 5.8 Hz, 1H), 7.56 (s, 1H), 7.60 (d, J = 8.0 Hz, 1H). 1.36 1
    117
    Figure US20160108025A1-20160421-C00196
         		MS (m + 1) = 366.1; 1H NMR (400 MHz, DMSO-d6) δ 3.71 (s, 3H), 4.34 (d, J = 6.0 Hz, 2H), 6.28 (t, J = 6.1 Hz, 1H), 6.81 (dd, J = 8.9, 2.9 Hz, 1H), 6.84 (d, J = 1.0 Hz, 1H), 6.87 (d, J = 2.8 Hz, 1H), 6.99 (d, J = 8.9 Hz, 1H), 7.19 (dd, J = 8.0, 1.4 Hz, 1H), 7.46 (s, 1H), 7.51 (d, J = 7.9 Hz, 1H). 1.17 1
    118
    Figure US20160108025A1-20160421-C00197
         		MS (m + 1) = 434.4; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (s, 2H), 4.66 (q, J = 8.9 Hz, 2H), 6.46-6.57 (m, 1H), 6.81 (dd, J = 9.0, 2.8 Hz, 1H), 6.89 (d, J = 2.8 Hz, 1H), 7.11 (d, J = 9.0 Hz, 1H), 7.20 (s, 1H), 7.27 (dd, J = 8.0, 1.4 Hz, 1H), 7.55 (s, 1H), 7.61 (d, J = 8.0 Hz, 1H). 1.32 1
    119
    Figure US20160108025A1-20160421-C00198
         		MS (m + 1) = 338.1; 1H NMR (400 MHz, DMSO-d6) δ 4.61 (d, J = 5.7 Hz, 2H), 6.63 (s, 2H), 7.20 (d, J = 7.3 Hz, 1H), 7.27-7.36 (m, 2H), 7.48 (d, J = 8.2 Hz, 1H), 7.90 (t, J = 5.8 Hz, 1H). 1.08 1
    120
    Figure US20160108025A1-20160421-C00199
         		MS (m − 1) = 369.9; 1H NMR (400 MHz, METHANOL-d4) δ 4.39 (s, 2H), 6.71 (s, 2H), 7.39-7.49 (m, 2H), 7.51- 7.61 (m, 1H), 7.68 (d, J = 1.0 Hz, 1H). 1.14 7
    121
    Figure US20160108025A1-20160421-C00200
         		MS (m + 1) = 343.8; 1H NMR (400 MHz, DMSO-d6) δ 0.86 (t, J = 7.3 Hz, 3H), 1.48 (sxt, J = 7.5 Hz, 2H), 2.43-2.48 (m, 2H), 4.29 (d, J = 5.6 Hz, 2H), 6.35 (t, J = 5.8 Hz, 1H), 6.51 (dd, J = 8.4, 2.4 Hz, 1H), 6.59 (d, J = 2.3 Hz, 1H), 6.95 (d, J = 8.3 Hz, 2H), 7.28 (66, J = 8.4, 1.7 Hz, 1H), 7.47 (d, J = 1.50 1
    8.4 Hz, 1H), 7.56 (d, J =
    1.1 Hz, 1H).
    122
    Figure US20160108025A1-20160421-C00201
         		MS (m + 1) = 377.9; 1H NMR (400 MHz, DMSO-d6) δ 0.88 (t, J = 7.3 Hz, 3H), 1.49 (sxt, J = 7.5 Hz, 2H), 2.45 (m, 2H), 4.35 (d, J = 5.5 Hz, 2H), 6.56 (t, J = 5.7 Hz, 1H), 6.76 (dd, J = 8.4, 2.20 Hz, 1H), 6.87 (d, J = 2.3 Hz, 1H), 7.10 (d, J = 1.49 3
    8.4 Hz, 1H), 7.23 (br. s., 1
    H), 7.37 (d, J = 8.4 Hz, 1
    H), 7.51-7.57 (m, 1H),
    7.64 (s, 1H).
    123
    Figure US20160108025A1-20160421-C00202
         		MS (m + 1) = 337.1; 1H NMR (400 MHz, DMSO-d6) δ 4.31 (d, J = 5.8 Hz, 2H), 6.59 (dd, J = 8.9, 2.7 Hz, 1H), 6.70 (t, J = 5.9 Hz, 1H), 6.77 (d, J = 2.7 Hz, 1H), 6.89 (d, J = 0.8 Hz, 1H), 7.19-7.28 (m, 2H), 7.46 (d, J = 8.5 Hz, 1H), 1.03 7
    7.55 (d, J = 1.1 Hz, 1H).
    124
    Figure US20160108025A1-20160421-C00203
         		MS (m + 1) = 363.8; 1H NMR (400 MHz, DMSO-d6) δ 1.10 (t, J = 7.5 Hz, 3H), 2.55 (q, J = 7.4 Hz, 2H), 4.33 (d, J = 5.8 Hz, 2H), 6.55 (t, J = 5.9 Hz, 1H), 6.77 (dd, J = 8.4, 2.2 Hz, 1 H), 6.87 (d, J = 2.3 Hz, 1 H), 6.94 (d, J = 0.6 Hz, 1 1.43 4
    H), 7.11 (d, J = 8.4 Hz, 1
    H), 7.28 (dd, J = 8.4, 1.7
    Hz, 1H), 7.46 (d, J = 8.4
    Hz, 1H), 7.57 (d, J = 0.9
    Hz, 1H).
    125
    Figure US20160108025A1-20160421-C00204
         		MS (m + 1) = 377.9; 1H NMR (400 MHz, DMSO-d6) δ 0.87 (t, J = 7.3 Hz, 3H), 1.50 (sxt, J = 7.5 Hz, 2H), 2.51-2.56 (m, 2H), 4.42 (br. s., 2H), 6.48 (dd, J = 8.6, 2.0 Hz, 1H), 6.59 (d, J = 1.8 Hz, 1H), 6.92 (br. s., 1H), 7.28 (d, J = 8.7 Hz, 1 H), 7.49 (dd, J = 8.7, 1.5 Hz, 1H), 7.63-7.69 (m, 2 1.49 3
    H), 7.73 (d, J = 1.0 Hz, 1
    H).
    126
    Figure US20160108025A1-20160421-C00205
         		MS (m + 1) = 343.7; 1H NMR (400 MHz, DMSO-d6) δ 0.86 (t, J = 7.3 Hz, 3H), 1.50 (sxt, J = 7.5 Hz, 2H), 2.47-2.54 (m, 2H), 4.29 (d, J = 5.7 Hz, 2H), 6.31 (t, J = 5.8 Hz, 1H), 6.43 (dd, J = 8.7, 2.8 Hz, 1H), 6.54 (d, J = 2.7 Hz, 1H), 6.92 (s, 1 1.46 3
    H), 7.00 (d, J = 8.6 Hz, 1
    H), 7.27 (dd, J = 8.4, 1.5
    Hz, 1H), 7.45 (d, J = 8.4
    Hz, 1H), 7.55 (s, 1H).
    127
    Figure US20160108025A1-20160421-C00206
         		MS (m + 1) = 476.2; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (s, 2H), 4.69 (q, J = 8.9 Hz, 2H), 6.46 (br. s., 1 H), 6.83 (dd, J = 8.9, 2.8 Hz, 1H), 6.93 (d, J = 2.8 Hz, 1H), 7.14 (d, J = 9.1 Hz, 1H), 7.72 (d, J = 0.6 Hz, 1H), 7.75-7.84 (m, 2 H). 1.32 1
    128
    Figure US20160108025A1-20160421-C00207
         		MS (m + 1) = 420.1; 1H NMR (400 MHz, DMSO-d6) δ 0.89 (t, J = 7.3 Hz, 3H), 1.50 (sxt, J = 7.5 Hz, 2H), 4.42 (s, 2H), 6.58 (br. s., 1 H), 6.78 (dd, J = 8.4, 2.3 Hz, 1H), 6.91 (d, J = 2.5 Hz, 1H), 7.14 (d, J = 8.4 Hz, 1H), 7.73 (s, 1H), 7.75- 1.67 3
    7.84 (m, 2H).
    129
    Figure US20160108025A1-20160421-C00208
         		MS (m + 1) = 378; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (br. s., 2H), 6.61 (dd, J = 8.8, 2.7 Hz, 1H), 6.74 (br. s., 1H), 6.82 (d, J = 2.7 Hz, 1H), 7.26 (d, J = 8.8 Hz, 1 H), 7.73 (d, J = 0.6 Hz, 1 H), 7.75-7.81 (m, 2H). 1.53 3
    130
    Figure US20160108025A1-20160421-C00209
         		MS (m + 1) = 462.1; 1H NMR (400 MHz, DMSO-d6) δ 4.47 (d, J = 2.9 Hz, 2H), 6.90 (dd, J = 9.1, 2.8 Hz, 1 H), 6.98-7.05 (m, 2H), 7.33 (d, J = 8.9 Hz, 1H), 7.74 (d, J = 0.6 Hz, 1H), 7.77-7.84 (m, 2H). 1.61 3
    131
    Figure US20160108025A1-20160421-C00210
         		MS (m + 1) = 472.1; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (br. s., 2H), 6.66 (dd, J = 8.9, 2.8 Hz, 1H), 6.80 (br. s., 1H), 6.95 (d, J = 2.8 Hz, 1H), 7.21 (dd, J = 9.0, 1.2 Hz, 1H), 7.75 (d, J = 0.6 Hz, 1H), 7.76-7.83 (m, 2 H). 1.38 1
    132
    Figure US20160108025A1-20160421-C00211
         		MS (m + 1) = 444.1; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (br. s., 2H), 6.79 (br. s., 1H), 6.84-6.89 (m, 1 H), 6.99 (d, J = 2.9 Hz, 1 H), 7.05 (t, J = 72 Hz, 1H), 7.17 (d, J = 8.8 Hz, 1H), 7.73 (d, J = 0.9 Hz, 1H), 7.75-7.84 (m, 2H). 1.51 3
    133
    Figure US20160108025A1-20160421-C00212
         		MS (m + 1) = 526.1; 1H NMR (400 MHz, DMSO-d6) δ 4.55 (d, J = 5.5 Hz, 2H), 7.29 (s, 2H), 7.40 (t, J = 5.7 Hz, 1H), 7.73 (s, 1H), 7.78- 7.85 (m, 2H). 1.45 1
    134
    Figure US20160108025A1-20160421-C00213
         		MS (m + 1) = 460.2; 1H NMR (400 MHz, DMSO-d6) δ 4.47 (s, 2H), 6.81 (dd, J = 9.0, 2.8 Hz, 1H), 6.97 (d, J = 2.8 Hz, 1H), 7.05 (t, J = 72.0 Hz, 1H), 7.18 (d, J = 8.9 Hz, 1H), 7.76 (s, 1H), 7.83 (s, 1H), 8.02 (d, J = 0.6 Hz, 1H). 1.34 1
    135
    Figure US20160108025A1-20160421-C00214
         		MS (m + 1) = 492.1; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (s, 2H), 4.69 (q, J = 8.9 Hz, 2H), 6.55 (br. s., 1 H), 6.77 (dd, J = 8.9, 2.8 Hz, 1H), 6.92 (d, J = 2.8 Hz, 1H), 7.14 (d, J = 9.1 Hz, 1H), 7.75 (d, J = 1.0 Hz, 1H), 7.83 (s, 1H), 8.01 (d, J = 0.6 Hz, 1H). 1.38 1
    136
    Figure US20160108025A1-20160421-C00215
         		MS (m + 1) = 490; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (br. s., 2H), 6.62 (dd, J = 9.0, 2.8 Hz, 1H), 6.86 (br. s., 1H), 6.93 (d, J = 2.7 Hz, 1H), 7.21 (dd, J = 8.9, 1.2 Hz, 1H), 7.75 (d, J = 0.9 Hz, 1H), 7.82 (s, 1H), 8.02 (s, 1H). 1.66 3
    137
    Figure US20160108025A1-20160421-C00216
         		MS (m + 1) = 542; 1H NMR (400 MHz, DMSO-d6) δ 4.56 (d, J = 5.4 Hz, 2H), 7.26 (s, 2H), 7.44 (t, J = 5.6 Hz, 1H), 7.74 (d, J = 0.7 Hz, 1H), 7.86 (s, 1H), 8.04 (s, 1H). 1.73 3
    138
    Figure US20160108025A1-20160421-C00217
         		MS (m + 1) = 428.1; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (d, J = 5.6 Hz, 2H), 6.62 (dd, J = 8.8, 1.8 Hz, 1 H), 6.84 (d, J = 2.1 Hz, 1 H), 7.32 (t, J = 5.8 Hz, 1H), 7.48 (d, J = 8.8 Hz, 1H), 7.72 (s, 1H), 7.80 (s, 1H), 8.03 (s, 1H). 1.4 1
    139
    Figure US20160108025A1-20160421-C00218
         		MS (m + 1) = 396; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 4.3 Hz, 2H), 6.57 (dd, J = 8.9, 2.8 Hz, 1 H), 6.74-6.85 (m, 2H), 7.27 (d, J = 8.8 Hz, 1H), 7.73 (s, 1H), 7.79 (s, 1H), 8.01 (s, 1H). 1.6 3
    140
    Figure US20160108025A1-20160421-C00219
         		MS (m + 1) = 474; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (s, 2H), 6.67 (dd, J = 9.1, 2.8 Hz, 1H), 6.78 (br. s., 1H), 6.95 (d, J = 2.8 Hz, 1H), 7.20 (dd, J = 8.9, 1.2 Hz, 1H), 7.45-7.54 (m, 1 H), 7.63 (dd, J = 8.6, 0.7 Hz, 1H), 7.80 (d, J = 0.9 Hz, 1H). 1.00 4
    141
    Figure US20160108025A1-20160421-C00220
         		MS (m + 1) = 442.2; 1H NMR (400 MHz, DMSO-d6) δ 4.46 (s, 2H), 6.78 (br. s., 1 H), 6.88 (dd, J = 9.0, 2.9 Hz, 1H), 6.98 (d, J = 2.8 Hz, 1H), 7.04 (t, J = 72.0 Hz, 1H), 7.17 (d, J = 8.8 Hz, 1H), 7.47-7.54 (m, 1 H), 7.62 (dd, J = 8.6, 0.86 Hz, 1H), 7.80 (d, J = 0.9 Hz, 1H). 1.51 3
    142
    Figure US20160108025A1-20160421-C00221
         		MS (m + 1) = 476.1; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (s, 2H), 4.68 (q, J = 8.8 Hz, 2H), 6.85 (dd, J = 8.9, 2.8 Hz, 1H), 6.92 (d, J = 2.8 Hz, 1H), 7.14 (d, J = 9.1 Hz, 1H), 7.46-7.54 (m, 1H), 7.61 (dd, J = 8.6, 0.9 Hz, 1H), 7.79 (d, J = 0.7 Hz, 1H). 1.55 3
    143
    Figure US20160108025A1-20160421-C00222
         		MS (m + 1) = 524.1; 1H NMR (400 MHz, DMSO-d6) δ 4.55 (d, J = 5.1 Hz, 2H), 7.30 (s, 2H), 7.39 (t, J = 5.6 Hz, 1H), 7.47-7.56 (m, 1 H), 7.61-7.67 (m, 1H), 7.80 (s, 1H). 1.05 4
    144
    Figure US20160108025A1-20160421-C00223
         		MS (m + 1) = 462.1; 1H NMR (400 MHz, DMSO-d6) δ 4.48 (br. s., 2H), 6.91 (dd, J = 9.1, 2.8 Hz, 1H), 7.00 (br. s., 1H), 7.02 (d, J = 2.9 Hz, 1H), 7.33 (d, J = 8.9 Hz, 1 H), 7.48-7.55 (m, 1H), 7.63 (dd, J = 8.6, 0.9 Hz, 1 H), 7.80 (d, J = 0.9 Hz, 1 H). 1.02 4
    145
    Figure US20160108025A1-20160421-C00224
         		MS (m + 1) = 444.1; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (br. s., 2H), 6.81- 6.85 (m, 1H), 6.88 (br. s., 1 H), 6.95 (d, J = 2.8 Hz, 1 H), 7.03 (t, J = 76.0 Hz, 1 H), 7.15 (d, J = 8.9 Hz, 1 H), 7.39 (d, J = 11.9 Hz, 1 H), 7.62 (s, 1H), 7.79 (d, J = 2.7 Hz, 1H). 0.94 4
    146
    Figure US20160108025A1-20160421-C00225
         		MS (m + 1) = 462; 1H NMR (400 MHz, DMSO-d6) δ 4.46 (br. s., 2H), 6.87 (dd, J = 9.1, 2.9 Hz, 1H), 7.00 (d, J = 2.9 Hz, 1H), 7.10 (br. s., 1H), 7.31 (d, J = 9.1 Hz, 1H), 7.41 (dd, J = 11.9, 1.2 Hz, 1H), 7.63 (d, J = 1.1 Hz, 1H), 7.82 (d, J = 2.8 Hz, 1H). 1.01 4
    147
    Figure US20160108025A1-20160421-C00226
         		MS (m + 1) = 476.1; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (s, 2H), 4.67 (q, J = 8.9 Hz, 2H), 6.81 (dd, J = 9.0, 2.8 Hz, 1H), 6.90 (d, J = 2.9 Hz, 1H), 7.12 (d, J = 8.9 Hz, 1H), 7.40 (dd, J = 11.9, 1.2 Hz, 1H), 7.62 (d, J = 1.1 Hz, 1H), 7.81 (d, J = 2.8 Hz, 1H). 0.98 4
    148
    Figure US20160108025A1-20160421-C00227
         		MS (m + 1) = 472; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (br. s., 2H), 6.64 (dd, J = 9.1, 2.8 Hz, 1H), 6.92 (d, J = 2.7 Hz, 2H), 7.15-7.23 (m, 1H), 7.39 (dd, J = 11.9, 1.2 Hz, 1H), 7.62 (d, J = 1.2 Hz, 1H), 7.81 (d, J = 2.8 Hz, 1H). 0.98 4
    149
    Figure US20160108025A1-20160421-C00228
         		MS (m + 1) = 456.3; 1H NMR (400 MHz, DMSO-d6) δ 4.35 (d, J = 5.7 Hz, 2H), 6.65 (dd, J = 9.0, 2.8 Hz, 1H), 6.80 (t, J = 5.8 Hz, 1H), 6.92 (d, J = 2.8 Hz, 1H), 7.14 (s, 1H), 7.18 (dq, J = 9.0, 1.3 Hz, 1H), 7.28 (dd, J = 8.4, 1.8 Hz, 1H), 7.59 (d, J = 8.5 Hz, 1H), 7.62 (d, J = 1.1 Hz, 1H). 1.35 1
    150
    Figure US20160108025A1-20160421-C00229
         		MS (m + 1) = 412.1; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (br. s., 2H), 6.86 (dd, J = 8.8, 2.8 Hz, 1H), 6.94 (br. s., 1H), 7.09 (d, J = 2.81 Hz, 1H), 7.35 (d, J = 8.68 Hz, 1H), 7.63-7.70 (m, 2 H), 7.73 (d, J = 5.75 Hz, 1 H). 1.35 1
    151
    Figure US20160108025A1-20160421-C00230
         		MS (m + 1) = 526.1; 1H NMR (400 MHz, DMSO-d6) δ 4.61 (d, J = 5.5 Hz, 2H), 7.30 (s, 2H), 7.39 (dd, J = 8.0, 6.17 Hz, 1H), 7.43 (t, J = 5.9 Hz, 1H), 7.62 (d, J = 8.1 Hz, 1H), 7.78 (d, J = 2.7 Hz, 1H). 1.05 5
    152
    Figure US20160108025A1-20160421-C00231
         		MS (m + 1) = 444.3; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 4.9 Hz, 2H), 6.75 (t, J = 5.3 Hz, 1H), 6.89 (dd, J = 8.9, 2.7 Hz, 1 H), 7.00 (d, J = 2.8 Hz, 1 H), 7.04 (t, J = 76 Hz, 1H), 7.13-7.19 (m, 2H), 7.47 (d, J = 10.0 Hz, 1H), 7.62 (d, J = 5.8 Hz, 1H). 1.27 1
    153
    Figure US20160108025A1-20160421-C00232
         		MS (m + 1) = 488.3; 1H NMR (400 MHz, DMSO-d6) δ 3.92 (s, 3H), 4.36 (s, 2H), 4.67 (q, J = 8.9 Hz, 2H), 6.40 (br. s., 1H), 6.79 (dd, J = 9.0, 2.63 Hz, 1H), 6.91 (d, J = 2.8 Hz, 1H), 7.12 (d, J = 9.1 Hz, 1H), 7.37 (s, 1 H), 7.55 (s, 1H), 7.65 (s, 1 H). 1.02 9
    154
    Figure US20160108025A1-20160421-C00233
         		MS (m + 1) = 476.2; 1H NMR (400 MHz, DMSO-d6) δ 4.46 (br. s., 2H), 4.68 (q, J = 8.9 Hz, 2H), 6.45 (br. s., 1H), 6.85 (dd, J = 9.0, 2.75 Hz, 1H), 6.94 (d, J = 2.1 Hz, 1H), 7.07 (t, J = 56.0 Hz, 1H), 7.14 (d, J = 8.9 Hz, 1H), 7.31 (dd, J = 8.1, 6.2 Hz, 1H), 7.43 (d, J = 2.8 Hz, 1H), 7.48 (d, J = 1.29 1
    8.1 Hz, 1H).
    155
    Figure US20160108025A1-20160421-C00234
         		MS (m + 1) = 495.2; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.4 Hz, 2H), 5.13 (s, 2H), 6.59 (t, J = 5.9 Hz, 1H), 6.83 (dd, J = 8.9, 2.8 Hz, 1H), 6.91-6.97 (m, 1H), 7.07 (s, 1H), 7.18- 7.23 (m, 1H), 7.30 (s, 1H), 7.68 (s, 1H), 8.01 (s, 1H). 1.25 1
    156
    Figure US20160108025A1-20160421-C00235
         		MS (m + 1) = 505.2; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (d, J = 5.8 Hz, 2H), 6.78-6.89 (m, 2H), 6.93- 7.00 (m, 2H), 7.03-7.09 (m, 1H), 7.14-7.25 (m, 2 H), 7.26 (s, 1H), 7.66 (s, 1 H), 8.00 (s, 1H). 1.35 1
    157
    Figure US20160108025A1-20160421-C00236
         		MS (m + 1) = 474.1; 1H NMR (400 MHz, DMSO-d6) δ 4.25 (td, J = 14.6, 3.67 Hz, 2H), 4.44 (br. s., 2H), 6.29 (tt, J = 52.0, 4.0 Hz, 1H), 6.47 (br. s., 1H), 6.79 (dd, J = 8.9, 2.8 Hz, 1H), 6.92 (d, J = 2.8 Hz, 1H), 7.11 (d, J = 9.1 Hz, 1H), 7.38 (s, 1 H), 7.68 (s, 1H), 7.85 (s, 1 H). 1.33 1
    158
    Figure US20160108025A1-20160421-C00237
         		MS (m + 1) = 446; 1H NMR (400 MHz, DMSO-d6) δ 4.53 (d, J = 5.8 Hz, 2H), 6.90-7.12 (m, 2H), 7.22 (d, J = 2.2 Hz, 2H), 7.37 (d, J = 0.7 Hz, 1H), 7.48 (t, J = 5.8 Hz, 1H), 7.57 (d, J = 9.9 Hz, 1H), 7.65 (d, J = 8.8 Hz, 1H), 7.71 (d, J = 5.8 Hz, 1H). 1.04 10
    159
    Figure US20160108025A1-20160421-C00238
         		MS (m + 1) = 526.2; 1H NMR (400 MHz, DMSO-d6) δ 4.51 (d, J = 5.6 Hz, 2H), 7.15 (d, J = 0.6 Hz, 1H), 7.31 (s, 2H), 7.37 (t, J = 5.8 Hz, 1H), 7.49 (d, J = 10.0 Hz, 1H), 7.68 (d, J = 5.9 Hz, 1H). 1.45 1
    160
    Figure US20160108025A1-20160421-C00239
         		MS (m + 1) = 430.1; 1H NMR (400 MHz, DMSO-d6) δ 1.11 (d, J = 6.9 Hz, 6 H), 4.41 (s, 2H), 6.41 (br. s., 1 H), 6.64 (dd, J = 8.5, 2.4 Hz, 1H), 6.83 (d, J = 2.5 Hz, 1H), 7.06 (d, J = 8.4 Hz, 1H), 7.60-7.72 (m, 3 H). 1.04 5
    161
    Figure US20160108025A1-20160421-C00240
         		MS (m + 1) = 422.2; 1H NMR (400 MHz, DMSO-d6) δ 1.25 (t, J = 7.0 Hz, 3H), 3.98 (q, J = 7.0 Hz, 2H), 4.43 (s, 2H), 6.83 (dd, J = 8.9, 2.8 Hz, 1H), 6.91 (d, J = 2.8 Hz, 1H), 7.02 (d, J = 8.9 Hz, 1H), 7.62-7.69 (m, 2H), 7.71 (d, J = 5.8 Hz, 1 H). 0.97 5
    162
    Figure US20160108025A1-20160421-C00241
         		MS (m + 1) = 458; 1H NMR (400 MHz, DMSO-d6) δ 4.25 (td, J = 14.6, 3.67 Hz, 2H), 4.40 (s, 2H), 6.85 (dd, J = 8.9, 2.8 Hz, 1H), 6.89- 7.00 (m, 2H), 7.10 (d, J = 8.9 Hz, 2H), 7.21 (d, J = 0.7 Hz, 2H), 7.48 (d, J = 10.0 Hz, 1H), 7.63 (d, J = 5.9 Hz, 1H). 0.98 10
    163
    Figure US20160108025A1-20160421-C00242
         		MS (m + 1) = 436.2; 1H NMR (400 MHz, DMSO-d6) δ 1.19 (d, J = 6.0 Hz, 6 H), 4.42 (s, 2H), 4.50 (dt, J = 12.1, 6.1 Hz, 1H), 6.83 (dd, J = 8.8, 2.8 Hz, 1H), 6.88 (d, J = 2.8 Hz, 1H), 7.04 (d, J = 8.9 Hz, 1H), 7.62-7.69 (m, 2H), 7.72 (d, J = 5.8 Hz, 1H). 1.36 1
    164
    Figure US20160108025A1-20160421-C00243
         		MS (m + 1) = 538.2; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.8 Hz, 2H), 4.68 (q, J = 8.9 Hz, 2H), 6.51 (t, J = 5.9 Hz, 1H), 6.79 (dd, J = 8.9, 2.8 Hz, 1 H), 6.93 (d, J = 2.8 Hz, 1 H), 7.07-7.17 (m, 3H), 7.63 (s, 1H), 7.93 (s, 1H). 1.47 1
    165
    Figure US20160108025A1-20160421-C00244
         		MS (m + 1) = 524.2; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (d, J = 5.6 Hz, 2H), 6.86 (dd, J = 9.1, 2.8 Hz, 1 H), 6.99-7.05 (m, 2H), 7.21 (d, J = 0.89 Hz, 2H), 7.33 (d, J = 8.9 Hz, 1H), 7.69 (s, 1H), 7.98 (s, 1H). 1.48 1
    166
    Figure US20160108025A1-20160421-C00245
         		MS (m + 1) = 456.2; 1H NMR (400 MHz, DMSO-d6) δ 3.92 (s, 3H), 4.38 (br. s., 2 H), 6.72 (br. s., 1H), 6.82 (dd, J = 8.9, 2.8 Hz, 1H), 6.97 (d, J = 2.8 Hz, 1H), 7.03 (t, J = 72.0 Hz, 1H), 7.15 (d, J = 8.9 Hz, 1H), 7.38 (s, 1H), 7.55 (s, 1H), 7.65 (d, J = 0.7 Hz, 1H). 1.31 1
    167
    Figure US20160108025A1-20160421-C00246
         		MS (m + 1) = 444.1; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (br. s., 2H), 6.82 (br. s., 1H), 6.88 (dd, J = 9.0, 2.9 Hz, 1H), 6.98 (d, J = 2.8 Hz, 1H), 7.04 (t, J = 76.0 Hz, 1H), 7.17 (d, J = 8.9 Hz, 1H), 7.38 (dd, J = 8.1, 6.1 Hz, 1H), 7.60 (d, J = 8.1 Hz, 1H), 7.77 (d, J = 2.8 Hz, 1H). 1.25 1
    168
    Figure US20160108025A1-20160421-C00247
         		MS (m + 1) = 476.1; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (br. s., 2H), 4.68 (q, J = 8.9 Hz, 2H), 6.42 (br. s., 1H), 6.87 (dd, J = 9.0, 2.8 Hz, 1H), 6.95 (d, J = 2.7 Hz, 1H), 7.14 (d, J = 8.9 Hz, 1H), 7.24 (s, 1H), 7.49 (d, J = 10.0 Hz, 1H), 7.64 (d, J = 5.9 Hz, 1H). 1.03 5
    169
    Figure US20160108025A1-20160421-C00248
         		MS (m + 1) = 462.1; 1H NMR (400 MHz, DMSO-d6) δ 4.53 (br. s., 2H), 6.91 (dd, J = 9.1, 2.9 Hz, 1H), 7.03 (d, J = 2.9 Hz, 2H), 7.33 (d, J = 8.9 Hz, 1H), 7.39 (dd, J = 8.1, 6.1 Hz, 1H), 7.61 (d, J = 8.1 Hz, 1H), 7.78 (d, J = 2.8 Hz, 1H). 1.37 1
    170
    Figure US20160108025A1-20160421-C00249
         		MS (m + 1) = 472.2; 1H NMR (400 MHz, DMSO-d6) δ 2.40 (s, 3H), 4.31 (d, J = 5.6 Hz, 2H), 4.68 (q, J = 8.9 Hz, 2H), 6.30 (t, J = 5.6 Hz, 1H), 6.83 (dd, J = 8.9, 2.7 Hz, 1H), 6.94 (d, J = 2.8 Hz, 1H), 7.01 (d, J = 1.0 Hz, 1H), 7.14 (d, J = 8.9 Hz, 1H), 7.44 (s, 1H), 7.48 (s, 1H). 1.05 5
    171
    Figure US20160108025A1-20160421-C00250
         		MS (m + 1) = 452; 1H NMR (400 MHz, DMSO-d6) δ 1.19 (d, J = 6.0 Hz, 6 H), 4.45 (s, 2H), 4.47-4.55 (m, 1H), 6.32 (br. s., 1H), 6.77 (dd, J = 8.9, 2.8 Hz, 1 H), 6.85 (d, J = 2.9 Hz, 1 H), 7.04 (d, J = 8.9 Hz, 1 H), 7.32-7.40 (m, 2H), 7.61 (d, J = 8.0 Hz, 1H). 1.57 3
    172
    Figure US20160108025A1-20160421-C00251
         		MS (m + 1) = 414.2; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.20-1.30 (m, 3H) 3.85-3.95 (m, 2H) 4.25- 4.35 (m, 2H) 6.06-6.23 (m, 1H) 6.49-6.62 (m, 1 H) 6.81-6.89 (m, 2H) 7.00- 7.08 (m, 1H) 7.19-7.27 (m, 1H) 7.49-7.64 (m, 2 H) 1.35 11
    173
    Figure US20160108025A1-20160421-C00252
         		MS (m + 1) = 498.3; 1H NMR (400 MHz, DMSO-d6) δ 1.20 (d, J = 6.0 Hz, 6 H), 4.39 (s, 2H), 4.50 (dt, J = 12.1, 6.1 Hz, 1H), 6.36 (br. s., 1H), 6.76 (dd, J = 9.0, 2.8 Hz, 1H), 6.86 (d, J = 2.8 Hz, 1H), 7.02 (t, J = 40 Hz, 1H), 7.07 (d, J = 3.7 Hz, 1H), 7.34 (s, 1H), 7.68 (s, 1H), 8.01 (s, 1H). 1.45 1
    174
    Figure US20160108025A1-20160421-C00253
         		MS (m + 1) = 401.2; 1H NMR (400 MHz, DMSO-d6) δ 3.67 (s, 3H), 4.33 (s, 2H), 6.60 (dd, J = 8.8, 2.7 Hz, 1H), 6.83-6.89 (m, 2H), 7.09 (s, 1H), 7.25 (dd, J = 8.0, 1.4 Hz, 1H), 7.52- 7.62 (m, 2H). 1.1 1
    175
    Figure US20160108025A1-20160421-C00254
         		MS (m + 1) = 462.3; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (d, J = 5.6 Hz, 2H), 6.89-6.95 (m, 1H), 7.00 (t, J = 5.8 Hz, 1H), 7.05 (d, J = 2.9 Hz, 1H), 7.33 (d, J = 9.1 Hz, 1H), 7.60 (s, 1H), 7.64 (d, J = 9.8 Hz, 1H), 7.74 (d, J = 5.8 Hz, 1H). 1.39 1
    176
    Figure US20160108025A1-20160421-C00255
         		MS (m + 1) = 396.1; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.9 Hz, 2H), 6.60 (t, J = 6.0 Hz, 1H), 6.86-6.96 (m, 2H), 7.07 (d, J = 0.9 Hz, 1H), 7.15- 7.23 (m, 1H), 7.44 (d, J = 10.0 Hz, 1H), 7.62 (d, J = 5.9 Hz, 1H). 1.29 1
    177
    Figure US20160108025A1-20160421-C00256
         		MS (m + 1) = 458.1; 1H NMR (400 MHz, DMSO-d6) δ 4.51 (d, J = 5.6 Hz, 2H), 6.71 (dd, J = 8.7, 2.1 Hz, 1 H), 7.25 (t, J = 5.8 Hz, 1H), 7.46 (d, J = 8.8 Hz, 1H), 7.65-7.70 (m, 2H), 7.73 (d, J = 5.8 Hz, 1H). 1.35 1
    178
    Figure US20160108025A1-20160421-C00257
         		MS (m + 1) = 484.2; 1H NMR (400 MHz, DMSO-d6) δ 1.25 (t, J = 7.0 Hz, 3H), 3.98 (q, J = 7.0 Hz, 2H), 4.38 (d, J = 3.8 Hz, 2H), 6.33 (br. s., 1H), 6.76 (dd, J = 8.9, 2.8 Hz, 1H), 6.89 (d, J = 2.8 Hz, 1H), 7.02 (d, J = 9.1 Hz, 1H), 7.12 (s, 1 H), 7.64 (s, 1H), 7.93 (s, 1 H). 1.4 1
    179
    Figure US20160108025A1-20160421-C00258
         		MS (m + 1) = 429; 1H NMR (400 MHz, DMSO-d6) δ 4.58 (d, J = 5.8 Hz, 2H), 7.19 (t, J = 5.9 Hz, 1H), 7.47 (d, J = 2.8 Hz, 1H), 7.65 (s, 1H), 7.83 (s, 1H), 7.98 (s, 1H), 8.03 (d, J = 2.8 Hz, 1H). 1.28 1
    180
    Figure US20160108025A1-20160421-C00259
         		MS (m + 1) = 424; 1H NMR (400 MHz, DMSO-d6) δ 4.37 (d, J = 5.8 Hz, 2H), 6.63-6.70 (m, 2H), 6.99 (d, J = 2.7 Hz, 1H), 7.07 (d, J = 0.9 Hz, 1H), 7.25 (d, J = 8.7 Hz, 1H), 7.44 (d, J = 10.2 Hz, 1H), 7.61 (d, J = 5.9 Hz, 1H). 1.35 1
    181
    Figure US20160108025A1-20160421-C00260
         		MS (m + 1) = 416; 1H NMR (400 MHz, DMSO-d6) δ 1.07 (t, J = 7.5 Hz, 3H), 2.52 (m, 2H), 4.42 (s, 2H), 6.41 (br. s., 1H), 6.60 (dd, J = 8.3, 2.5 Hz, 1H), 6.84 (d, J = 2.5 Hz, 1H), 7.02 (d, J = 8.3 Hz, 1H), 7.59-7.71 (m, 3H). 1 5
    182
    Figure US20160108025A1-20160421-C00261
         		MS (m + 1) = 406; 1H NMR (400 MHz, DMSO-d6) δ 4.37 (d, J = 5.9 Hz, 2H), 6.64 (dd, J = 8.8, 2.7 Hz, 1H), 6.74 (t, J = 6.0 Hz, 1H), 6.95 (d, J = 2.7 Hz, 1H), 7.05 (d, J = 0.9 Hz, 1H), 7.23 (dd, J = 8.5, 2.5 Hz, 2H), 7.54-7.61 (m, 2H). 1.31 1
    183
    Figure US20160108025A1-20160421-C00262
         		MS (m + 1) = 472.1; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (br. s., 2H), 6.69 (dd, J = 8.9, 2.81 Hz, 1H), 6.80 (br. s., 1H), 6.98 (d, J = 2.8 Hz, 1H), 7.21 (dd, J = 8.9, 1.2 Hz, 1H), 7.62-7.71 (m, 2H), 7.73 (d, J = 5.8 Hz, 1 H). 1.04 5
    184
    Figure US20160108025A1-20160421-C00263
         		MS (m + 1) = 477.9; 1H NMR (400 MHz, DMSO-d6) δ 4.54 (d, J = 5.8 Hz, 2H), 6.86 (dd, J = 9.1, 2.8 Hz, 1 H), 7.00-7.06 (m, 2H), 7.07 (t, J = 52 Hz, 1H), 7.33 (d, J = 9.3 Hz, 1H), 7.51 (s, 1H), 7.68 (d, J = 8.1 Hz, 1H). 1.62 3
    185
    Figure US20160108025A1-20160421-C00264
         		MS (m + 1) = 534; 1H NMR (400 MHz, DMSO-d6) δ 4.46 (d, J = 4.5 Hz, 2H), 6.84 (t, J = 5.3 Hz, 1H), 6.90 (t, J = 72.0 Hz, 1H), 6.97 (s, 2H), 7.64-7.69 (m, 2H), 7.74 (d, J = 5.8 Hz, 1H). 1.52 1
    186
    Figure US20160108025A1-20160421-C00265
         		MS (m + 1) = 428; 1H NMR (400 MHz, DMSO-d6) δ 4.46 (br. s., 2H), 6.66 (dd, J = 9.1, 2.8 Hz, 1H), 6.83 (d, J = 2.7 Hz, 2H), 7.23 (dd, J = 9.1, 1.2 Hz, 1H), 7.63- 7.70 (m, 2H), 7.73 (d, J = 5.8 Hz, 1H). 1.61 3
    187
    Figure US20160108025A1-20160421-C00266
         		MS (m + 1) = 492; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (d, J = 2.9 Hz, 2H), 4.68 (q, J = 8.8 Hz, 2H), 6.53 (br. s., 1H), 6.79 (dd, J = 9.1, 2.8 Hz, 1H), 6.91 (d, J = 2.8 Hz, 1H), 7.07 (t, J = 52 Hz, 1H), 7.14 (d, J = 9.1 Hz, 1H), 7.39 (d, J = 8.1 Hz, 1H), 7.52 (s, 1H), 7.66 (d, J = 8.1 Hz, 1H). 1.56 3
    188
    Figure US20160108025A1-20160421-C00267
         		MS (m + 1) = 414.1; 1H NMR (400 MHz, DMSO-d6) δ 2.37 (d, J = 0.9 Hz, 3H), 4.47 (s, 2H), 6.44 (d, J = 1.1 Hz, 1H), 6.55 (d, J = 2.1 Hz, 1H), 6.70 (d, J = 2.1 Hz, 1H), 7.66 (s, 1H), 7.72 (s, 1H), 7.96 (s, 1H). 1.39 1
    189
    Figure US20160108025A1-20160421-C00268
         		MS (m + 1) = 542.3; 1H NMR (400 MHz, DMSO-d6) δ 4.59 (d, J = 5.6 Hz, 2H), 7.28 (s, 2H), 7.44 (t, J = 5.8 Hz, 1H), 7.67 (s, 1H), 7.82 (s, 1H), 7.99 (s, 1H). 1.52 1
    190
    Figure US20160108025A1-20160421-C00269
         		MS (m + 1) = 370.2; 1H NMR (400 MHz, DMSO-d6) δ 0.85 (t, J = 7.3 Hz, 3H), 1.47 (sxt, J = 7.4 Hz, 2H), 2.38 (t, J = 7.5 Hz, 2H), 4.41 (s, 2H), 6.31-6.45 (m, 3 H), 6.93 (t, J = 8.6 Hz, 1H), 7.62-7.72 (m, 3H). 1.59 4
    191
    Figure US20160108025A1-20160421-C00270
         		MS (m + 1) = 463.2; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 5.8 Hz, 2H), 6.85 (t, J = 5.9 Hz, 1H), 6.92-6.98 (m, 2H), 7.00 (d, J = 2.9 Hz, 1H), 7.14 (t, J = 76, 1H), 7.20 (s, 1H), 7.35 (s, 1H), 7.67 (s, 1H), 8.03 (s, 1H). 1.16 1
    192
    Figure US20160108025A1-20160421-C00271
         		MS (m + 1) = 412.1; 1H NMR (400 MHz, DMSO-d6) δ 4.45 (d, J = 3.2 Hz, 2H), 6.50 (dt, J = 9.1, 1.4 Hz, 1 H), 6.63 (dd, J = 13.6, 2.7 Hz, 1H), 6.85 (br. s., 1H), 7.20 (td, J = 9.0, 0.9 Hz, 1 H), 7.62-7.70 (m, 2H), 7.73 (d, J = 5.8 Hz, 1H). 1 4
    193
    Figure US20160108025A1-20160421-C00272
         		MS (m + 1) = 474; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (br. s., 2H), 6.67 (dd, J = 8.9, 2.8 Hz, 1H), 6.83 (br. s., 1H), 6.95 (d, J = 2.8 Hz, 1H), 7.20 (dd, J = 9.1, 1.2 Hz, 1H), 7.37 (dd, J = 8.0, 6.2 Hz, 1H), 7.60 (d, J = 8.1 Hz, 1H), 7.78 (d, J = 2.8 Hz, 1H). 1.35 1
    194
    Figure US20160108025A1-20160421-C00273
         		MS (m + 1) = 380.1; 1H NMR (400 MHz, DMSO-d6) δ 2.37 (d, J = 1.1 Hz, 3H), 4.38 (s, 2H), 6.26 (s, 1H), 6.42 (d, J = 1.2 Hz, 1H), 6.60 (d, J = 2.1 Hz, 1H), 6.67 (d, J = 2.1 Hz, 1H), 7.08 (d, J = 0.9 Hz, 1H), 7.27 (dd, J = 8.0, 1.4 Hz, 1H), 7.57 (d, J = 8.0 Hz, 1H), 7.61 (s, 1H). 1.24 1
    195
    Figure US20160108025A1-20160421-C00274
         		MS (m + 1) = 392.1; 1H NMR (400 MHz, DMSO-d6) δ 2.24 (s, 3H), 4.48 (br. s., 2 H), 6.67 (s, 2H), 6.73 (d, J = 8.0 Hz, 2H), 7.62-7.70 (m, 2H), 7.72 (d, J = 5.8 Hz, 1H). 1.55 3
    196
    Figure US20160108025A1-20160421-C00275
         		MS (m + 1) = 412.1; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (d, J = 5.4 Hz, 2H), 6.69 (dd, J = 8.7, 2.0 Hz, 1 H), 6.88 (d, J = 2.2 Hz, 1 H), 7.28 (t, J = 5.8 Hz, 1H), 7.47 (d, J = 8.8 Hz, 1H), 7.64-7.71 (m, 2H), 7.74 (d, J = 5.8 Hz, 1H). 1.35 1
    197
    Figure US20160108025A1-20160421-C00276
         		MS (m + 1) = 401.1; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (d, J = 5.8 Hz, 2H), 6.78 (t, J = 6.1 Hz, 1H), 6.95 (d, J = 1.6 Hz, 1H), 6 97-7.02 (m, 1H), 7.06 (d, J = 12.5 Hz, 1H), 7.13 (t, J = 76.0 Hz, 1H), 7.19 (d, J = 8.1 Hz, 2H), 7.35 (s, 1H), 7.55 (d, J = 9.9 Hz, 1 H), 7.67 (d, J = 5.9 Hz, 1 0.87 5
    H).
    198
    Figure US20160108025A1-20160421-C00277
         		MS (m + 1) = 428.2; 1H NMR (400 MHz, DMSO-d6) δ 4.59 (d, J = 5.6 Hz, 2H), 7.28 (s, 2H), 7.43 (t, J = 5.8 Hz, 1H), 7.64 (s, 1H), 7.82 (s, 1H), 7.98 (s, 1H). 1.43 1
    199
    Figure US20160108025A1-20160421-C00278
         		MS (m + 1) = 426.1; 1H NMR (400 MHz, DMSO-d6) δ 4.46 (br. s., 2H), 6.58 (dd, J = 8.9, 2.8 Hz, 1H), 6.71 (br. s., 1H), 6.75 (d, J = 2.8 Hz, 1H), 6.97 (7, J = 72.0 Hz, 1 H), 7.09 (d, J = 8.9 Hz, 1 H), 7.66 (d, J = 0.7 Hz, 1 H), 7.71 (s, 1H), 7.96 (s, 1 H). 1.49 3
    200
    Figure US20160108025A1-20160421-C00279
         		MS (m + 1) = 463.2; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 5.8 Hz, 2H), 6.85 (t, J = 5.9 Hz, 1H), 6.92-6.98 (m, 2H), 7.00 (d, J = 2.9 Hz, 1H), 7.14 (t, J = 76, 1H), 7.20 (s, 1H), 7.35 (s, 1H), 7.67 (s, 1H), 8.03 (s, 1H). 1.21 1
    201
    Figure US20160108025A1-20160421-C00280
         		MS (m + 1) = 446.1; 1H NMR (400 MHz, DMSO-d6) δ 4.51 (d, J = 5.3 Hz, 2H), 6.94 (dd, J = 5.0, 2.9 Hz, 2 H), 7.02 (dd, J = 5.8, 2.9 Hz, 1H), 7.67 (d, J = 0.7 Hz, 1H), 7.79 (s, 1H), 7.98 (s, 1H). 1.47 1
    202
    Figure US20160108025A1-20160421-C00281
         		MS (m + 1) = 417.3; 1H NMR (400 MHz, DMSO-d6) δ 4.48 (d, J = 5.6 Hz, 2H), 6.79 (t, J = 5.7 Hz, 1H), 6.92-6.97 (m, 1H), 7.01 (d, J = 2.9 Hz, 1H), 7.16 (s, 1H), 7.19 (d, J = 8.9 Hz, 1 H), 7.23 (d, J = 72.0 Hz, 1 H), 7.30 (d, J = 8.1 Hz, 1 H), 7.57 (d, J = 8.0 Hz, 1 H). 1.15 1
    203
    Figure US20160108025A1-20160421-C00282
         		MS (m + 1) = 396.1; 1H NMR (400 MHz, DMSO-d6) δ 4.51 (d, J = 5.6 Hz, 2H), 6.54-6.66 (m, 2H), 7.32 (t, J = 5.7 Hz, 1H), 7.38 (t, J = 8.7 Hz, 1H), 7.64-7.69 (m, 2H), 7.74 (d, J = 5.8 Hz, 1 H). 1.51 3
    204
    Figure US20160108025A1-20160421-C00283
         		MS (m + 1) = 395.1; 1H NMR (400 MHz, DMSO-d6) δ 4.52 (d, J = 5.9 Hz, 2H), 7.23 (t, J = 6.0 Hz, 1H), 7.29-7.37 (m, 2H), 7.44 (d, J = 2.9 Hz, 1H), 7.65- 7.72 (m, 2H), 8.02 (d, J = 2.9 Hz, 1H). 1.17 1
    205
    Figure US20160108025A1-20160421-C00284
         		MS (m + 1) = 442.1; 1H NMR (400 MHz, DMSO-d6) δ 4.36 (br. s., 2H), 4.60 (q, J = 8.9 Hz, 2H), 6.28 (br. s., 1H), 6.59 (dd, J = 8.9, 2.8 Hz, 1H), 6.74 (d, J = 2.7 Hz, 1H), 7.03 (d, J = 8.9 Hz, 1H), 7.16 (s, 1H), 7.46 (d, J = 10.0 Hz, 1H), 7.61 (d, J = 5.9 Hz, 1H). 1.31 1
    206
    Figure US20160108025A1-20160421-C00285
         		MS (m + 1) = 438; 1H NMR (400 MHz, DMSO-d6) δ 1.25 (t, J = 7.0 Hz, 3H) 3.98 (q, J = 7.0 Hz, 2H), 4.46 (s, 2H), 6.33 (br. s., 1 H), 6.74-6.79 (m, 1H), 6.88 (s, 1H), 7.02 (s, 1H), 7.37 (d, J = 8.1 Hz, 1H), 7.40 (s, 1H), 7.62 (d, J = 8.1 Hz, 1H). 1.51 3
    207
    Figure US20160108025A1-20160421-C00286
         		MS (m + 1) = 436.2; 1H NMR (400 MHz, DMSO-d6) δ 1.14 (d, J = 6.9 Hz, 6 H), 3.01-3.14 (m, 2H), 4.44 (d, J = 3.7 Hz, 2H), 6.62 (br. s., 1H), 6.81 (dd, J = 8.6, 2.32 Hz, 1H), 6.88 (s, 1H), 7.21 (s, 1H), 7.31 (d, J = 8.6 Hz, 1H), 7.66 (s, 1 H), 7.79 (s, 1H). 1.6 3
    208
    Figure US20160108025A1-20160421-C00287
         		MS (m + 1) = 378.1; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (d, J = 4.4 Hz, 2H), 6.64 (dd, J = 8.8, 2.7 Hz, 1 H), 6.74 (br. s., 1H), 6.84 (d, J = 2.7 Hz, 1H), 7.26 (d, J = 8.8 Hz, 1H), 7.61-7.67 (m, 2H), 7.71 (d, J = 5.9 Hz, 1H). 1.33 1
    209
    Figure US20160108025A1-20160421-C00288
         		MS (m + 1) = 363.3; 1H NMR (400 MHz, DMSO-d6) δ 2.52 (s, 3H), 4.55 (s, 2H), 7.05 (d, J = 2.1 Hz, 1H), 7.10 (dd, J = 8.8, 2.2 Hz, 1H), 7.47 (dd, J = 8.2, 1.3 Hz, 1H), 7.69 (d, J = 0.9 Hz, 1H), 7.74-7.82 (m, 3H). 1.07 1
    210
    Figure US20160108025A1-20160421-C00289
         		MS (m + 1) = 449.3; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (d, J = 5.3 Hz, 2H), 5.13 (s, 2H), 6.56 (t, J = 5.8 Hz, 1H), 6.83 (dd, J = 8.9, 2.8 Hz, 1H), 6.94 (d, J = 3.1 Hz, 1H), 7.13 (d, J = 44.0 Hz, 1H), 7.20 (d, J = 2.8 Hz, 1H), 7.32 (s, 1H), 7.35 (d, J = 8.1 Hz, 1H), 7.61 (d, J = 8.1 Hz, 1H). 1.18 1
    211
    Figure US20160108025A1-20160421-C00290
         		MS (m + 1) = 388.1; 1H NMR (400 MHz, DMSO-d6) δ 1.26 (t, J = 7.0 Hz, 3H), 3.92 (q, J = 7.0 Hz, 2H), 4.39 (s, 2H), 6.56 (dd, J = 8.8, 2.8 Hz, 1H), 6.72 (d, J = 2.8 Hz, 1H), 6.90 (d, J = 8.9 Hz, 1H), 7.64 (d, J = 9.8 Hz, 1H), 7.67-7.73 (m, 2H). 0.92 5
    212
    Figure US20160108025A1-20160421-C00291
         		MS (m + 1) = 444.2; 1H NMR (400 MHz, DMSO-d6) δ 4.49 (d, J = 5.4 Hz, 2H), 6.53-6.60 (m, 2H), 6.68 (t, J = 1.9 Hz, 1H), 7.07 (t, J = 5.8 Hz, 1H), 7.67 (s, 1H), 7.76 (s, 1H), 7.97 (s, 1H). 1.5 1
    213
    Figure US20160108025A1-20160421-C00292
         		MS (m + 1) = 408.2; 1H NMR (400 MHz, DMSO-d6) δ 2.24 (s, 3H), 4.50 (br. s., 2 H), 6.68 (s, 2H), 6.70-6.79 (m, 2H), 7.67 (d, J = 0.7 Hz, 1H), 7.72 (s, 1H), 7.97 (s, 1H). 1.43 1
    214
    Figure US20160108025A1-20160421-C00293
         		MS (m + 1) = 362.1; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (br. s., 2H), 6.51 (dt, J = 8.8, 1.39 Hz, 1H), 6.61 (dd, J = 12.5, 2.7 Hz, 1H), 6.77 (br. s., 1H), 7.20 (t, J = 8.7 Hz, 1H), 7.62-7.69 (m, 2H), 7.71 (d, J = 5.9 Hz, 1H). 1.26 1
    215
    Figure US20160108025A1-20160421-C00294
         		MS (m + 1) = 362.1; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (s, 2H), 6.47 (br. s., 1 H), 6.57-6.63 (m, 1H), 6.76 (dd, J = 6.3, 2.9 Hz, 1 H), 7.11 (t, J = 9.2 Hz, 1H), 7.65 (d, J = 9.8 Hz, 1H), 7.68 (d, J = 0.9 Hz, 1H), 7.71 (d, J = 5.8 Hz, 1H). 1.46 1
    216
    Figure US20160108025A1-20160421-C00295
         		MS (m + 1) = 444.2; 1H NMR (400 MHz, DMSO-d6) δ ppm 0.90-1.00 (m, 6 H) 1.88-2.01 (m, 1H) 3.58- 3.67 (m, 2H) 4.28-4.40 (m, 2H) 6.53-6.63 (m, 1 H) 6.80-6.88 (m, 2H) 6.93- 7.13 (m, 1H) 7.16-7.21 (m, 1H) 7.23-7.31 (m, 1 H) 7.55-7.66 (m, 2H) 1.52 11
    217
    Figure US20160108025A1-20160421-C00296
         		MS (m + 1) = 404.1; 1H NMR (400 MHz, DMSO-d6) δ 1.27 (t, J = 7.0 Hz, 3H), 3.92 (q, J = 7.0 Hz, 2H), 4.42 (s, 2H), 6.51 (dd, J = 8.8, 2.8 Hz, 1H), 6.69 (d, J = 2.7 Hz, 1H), 6.91 (d, J = 8.8 Hz, 1H), 7.67 (d, J = 0.9 Hz, 1H), 7.70 (s, 1H), 7.95 (s, 1H). 1.5 3
    218
    Figure US20160108025A1-20160421-C00297
         		MS (m + 1) = 394.3; 1H NMR (400 MHz, DMSO-d6) δ 4.50 (d, J = 5.8 Hz, 2H), 6.53-6.62 (m, 1H), 6.67 (t, J = 9.8 Hz, 1H), 6.92 (d, J = 9.0 Hz, 1H), 7.20 (dd, J = 11.9, 2.1 Hz, 1H), 7.30 (d, J = 0.9 Hz, 1H), 7.32 (dd, J = 8.2, 1.3 Hz, 1H), 7.60- 1.3 1
    7.70 (m, 2H).
    219
    Figure US20160108025A1-20160421-C00298
         		MS (m + 1) = 422.3; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.8 Hz, 2H), 6.80 (t, J = 5.9 Hz, 1H), 6.90 (d, J = 2.8 Hz, 1H), 7.00 (dd, J = 9.2, 2.8 Hz, 1H), 7.06 (d, J = 1.0 Hz, 1H), 7.17 (dt, J = 9.1, 1.1 Hz, 1H), 7.26 (dd, J = 8.0, 1.32 1
    1.4 Hz, 1H), 7.59 (d, J = 8.0
    Hz, 1H), 7.61 (s, 1H).
    220
    Figure US20160108025A1-20160421-C00299
         		MS (m + 1) = 416.3; 1H NMR (400 MHz, DMSO-d6) δ 0.91 (t, J = 7.3 Hz, 3H), 1.33-1.48 (m, 2H), 2.18 (s, 3H), 4.42 (s, 2H), 6.38 (br. s., 1H), 6.42-6.49 (m, 2H), 7.62 (s, 1H), 7.69 (s, 1H), 7.94 (s, 1H). 1.59 1
    221
    Figure US20160108025A1-20160421-C00300
         		MS (m + 1) = 426.2; 1H NMR (400 MHz, DMSO-d6) δ 3.54 (q, J = 11.4 Hz, 3H), 4.43 (s, 2H), 6.41 (br. s., 1 H), 6.57 (dt, J = 8.9, 3.5 Hz, 1H), 6.65 (dd, J = 6.1, 2.9 Hz, 1H), 6.98 (t, J = 9.2 Hz, 1H), 7.65 (s, 1H), 7.69 (s, 1H), 7.95 (s, 1H). 1.34 1
    222
    Figure US20160108025A1-20160421-C00301
         		MS (m + 1) = 428.3; 1H NMR (400 MHz, DMSO-d6) δ 4.53 (d, J = 5.9 Hz, 2H), 6.45 (s, 1H), 6.60 (d, J = 2.3 Hz, 1H), 6.80 (dd, J = 9.0, 2.3 Hz, 1H), 7.10 (d, J = 0.9 Hz, 1H), 7.27 (dd, J = 7.9, 1.5 Hz, 1H), 7.36-7.44 (m, 1H), 7.58-7.63 (m, 2H), 7.71 (t, J = 6.1 Hz, 1H). 1.19 1
    223
    Figure US20160108025A1-20160421-C00302
         		MS (m + 1) = 436.1; 1H NMR (400 MHz, DMSO-d6) δ 4.43 (d, J = 5.9 Hz, 2H), 6.77-6.84 (m, 2H), 6.90 (s, 1H), 6.96 (d, J = 2.7 Hz, 1H), 7.04 (t, J = 76.0 Hz, 1 H), 7.15 (d, J = 8.9 Hz, 1 H), 7.53 (s, 1H), 7.72 (s, 1 H). 1.6 4
    224
    Figure US20160108025A1-20160421-C00303
         		MS (m + 1) = 468; 1H NMR (400 MHz, DMSO-d6) δ 4.42 (d, J = 5.8 Hz, 2H), 4.68 (q, J = 8.9 Hz, 2H), 6.50 (t, J = 6.0 Hz, 1H), 6.78 (dd, J = 9.0, 2.75 Hz, 1 H), 6.91 (d, J = 2.8 Hz, 1 H), 7.08-7.22 (m, 3H), 7.59 (s, 1H), 7.79 (s, 1H). 1.4 1
    225
    Figure US20160108025A1-20160421-C00304
         		MS (m + 1) = 418.3; 1H NMR (400 MHz, DMSO-d6) δ 4.34 (d, J = 5.9 Hz, 2H), 4.59 (q, J = 9.0 Hz, 2H), 6.27 (t, J = 6.1 Hz, 1H), 6.56 (dd, J = 8.9, 2.8 Hz, 1 H), 6.72 (d, J = 2.7 Hz, 1 H), 6.98-7.08 (m, 2H), 7.43 (d, J = 10.0 Hz, 1H), 7.52 (d, J = 5.9 Hz, 1H). 0.93 9
    226
    Figure US20160108025A1-20160421-C00305
         		MS (m + 1) = 404.3; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (d, J = 5.9 Hz, 2H), 6.63 (dd, J = 9.1, 2.8 Hz, 1 H), 6.77 (t, J = 6.0 Hz, 1H), 6.80 (d, J = 2.8 Hz, 1H), 7.13 (br. s., 2H), 7.21 (dd, J = 8.9, 1.2 Hz, 1H), 7.47 (d, J = 10.0 Hz, 1H), 7.57 (d, J = 0.97 9
    5.8 Hz, 1H).
    227
    Figure US20160108025A1-20160421-C00306
         		MS (m + 1) = 448.2; 1H NMR (400 MHz, DMSO-d6) δ 4.39 (d, J = 5.9 Hz, 2H), 6.67 (dd, J = 9.0, 2.8 Hz, 1 H), 6.75 (t, J = 5.9 Hz, 1H), 6.95 (d, J = 2.8 Hz, 1H), 7.13 (br. s., 1H), 7.19 (dd, J = 8.9, 1.2 Hz, 2H), 7.49 (d, J = 9.9 Hz, 1H), 7.58 (d, J = 0.98 9
    5.8 Hz, 1H).
    228
    Figure US20160108025A1-20160421-C00307
         		MS (m + 1) = 420.3; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (d, J = 5.8 Hz, 2H), 6.68 (dd, J = 8.7, 2.6 Hz, 1 H), 6.91 (d, J = 2.6 Hz, 1 H), 7.12 (br. s., 2H), 7.25 (t, J = 5.8 Hz, 1H), 7.44-7.52 (m, 2H), 7.58 (d, J = 5.9 Hz, 1H). 1.01 9
    229
    Figure US20160108025A1-20160421-C00308
         		MS (m + 1) = 501.8; 1H NMR (400 MHz, DMSO-d6) δ 4.51 (d, J = 5.9 Hz, 2H), 7.23 (br. s., 1H), 7.29 (s, 2 H), 7.35 (t, J = 5.81 Hz, 1H), 7.52 (d, J = 9.9 Hz, 1H), 7.65 (d, J = 5.6 Hz, 1H). 1.04 9
    230
    Figure US20160108025A1-20160421-C00309
         		MS (m + 1) = 420.3; 1H NMR (400 MHz, DMSO-d6) δ 4.44 (d, J = 5.9 Hz, 2H), 6.76 (t, J = 6.1 Hz, 1H), 6.84-6.89 (m, 1H), 6.98 (d, J = 2.9 Hz, 1H), 7.04 (t, J = 72.0 Hz, 1H), 7.16 (d, J = 8.9 Hz, 1H), 7.29 (br. s., 1H), 7.52 (d, J = 9.9 Hz, 1 0.94 9
    H), 7.60 (d, J = 5.8 Hz, 1
    H).
    231
    Figure US20160108025A1-20160421-C00310
         		MS (m + 1) = 542.3; 1H NMR (400 MHz, DMSO-d6) δ 4.41 (d, J = 5.5 Hz, 2H), 4.68 (q, J = 8.8 Hz, 2H), 6.42 (t, J = 6.0 Hz, 1H), 6.84 (dd, J = 9.0, 2.75 Hz, 1 H), 6.93 (d, J = 2.8 Hz, 1 H), 7.13 (d, J = 9.1 Hz, 2 H), 7.30 (br. s., 1H), 7.51 0.97 9
    (d, J = 9.9 Hz, 1H), 7.60 (d,
    J = 5.8 Hz, 1H).
    232
    Figure US20160108025A1-20160421-C00311
         		MS (m + 1) = 388.3; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.9 Hz, 2H), 6.86 (s, 2H), 6.89 (t, J = 5.9 Hz, 1H), 7.12 (br. s., 1H), 7.48 (d, J = 9.9 Hz, 1H), 7.59 (d, J = 5.8 Hz, 1H). 0.98 9
    233
    Figure US20160108025A1-20160421-C00312
         		MS (m + 2) = 456.2; 1H NMR (400 MHz, DMSO-d6) δ 4.40 (d, J = 5.6 Hz, 2H), 6.66 (dd, J = 9.0, 2.8 Hz, 1H), 6.84 (t, J = 5.9 Hz, 1H), 6.93 (d, J = 2.8 Hz, 1H), 7.15-7.20 (m, 2H), 7.27 (dd, J = 8.0, 1.4 Hz, 1H), 7.60-7.65 (m, 2H). 1.35 1
    • Biological Example 1
  • A patch-clamp assay on the QPatch© automated patch clamp system was employed to assesses whether compounds functionally enhance the cardiac delayed rectifier hERG (human ether-a-go-go-related gene) potassium channel. The assay measures electric the current passing through hERG channels that are heterologously expressed in a stable Chinese hamster ovary (CHO) cell line. Channels are opened by a hERG-specific voltage protocol and the compound effect is directly characterized by the activation of the hERG current. EC50 values are obtained from fitting 4-concentration dose response curves (1.1, 3.3, 10 & 30 uM) in triplicates at 4 different sections of the voltage protocol (steady state current amplitude at +10 mV, at +30 mV, peak tail current amplitude and tail current amplitude at 7 second). In the absence of a clear trend of saturation at 30 uM, only increased % current values for the 4 parameters are utilized.
  • Activity Table: hERG Activator EC -QPatch hERG activator
    4-concentration EC50 assay % change@TL7@10 uM
    Ex % change
    1  166*
    2  126*
    3  121*
    4  155*
    5 146
    6 264
    7 198
    8 128
    9  78
    10 285
    11 129
    12  85
    13  39
    14 196
    15 162
    16 521
    17 477
    18 409
    19 394
    20 340
    21 333
    22 328
    23 290
    24 280
    25 269
    26 267
    27 261
    28 260
    29 258
    30 228
    31 218
    32 193
    33 192
    34 191
    35 180
    36 174
    37 170
    38 164
    39 164
    40 161
    41 160
    42 159
    43 148
    44 146
    45 145
    46 139
    47 131
    48 123
    49 106
    50 100
    51  99
    52  95
    53  95
    54  94
    55  90
    56  88
    57  76
    58  71
    59  61
    60  58
    61  47
    62  43
    63  34
    64 348
    65 284
    66 261
    67 247
    68 224
    69 221
    70 200
    71 193
    72 176
    73 132
    74 124
    75 123
    76 120
    77 118
    78 108
    79 101
    80  83
    81  74
    82  39
    83  36
    84  29
    85 397
    86 381
    87 326
    88 274
    89 270
    90 247
    91 226
    92 215
    93 212
    94 194
    95 193
    96 185
    97 159
    98 158
    99 157
    100 156
    101 156
    102 153
    103 112
    104 111
    105 105
    106  90
    107  85
    108  82
    109  81
    110  76
    111  65
    112  53
    113  53
    114  45
    115  41
    116  31
    117  28
    118  27
    119  22
    120 282
    121 210
    122 184
    123 183
    124 167
    125 138
    126  64
    127 268
    128 142
    129 154
    130 220
    131 209
    132 371
    133 326
    134 217
    135 181
    136 143
    137 166
    138 196
    139 112
    140 290
    141 144
    142 188
    143 193
    144 236
    145 103
    146 171
    147 151
    148 201
    149 335
    150 218
    151 308
    152  333*
    153 381
    154 325
    155 370
    156 356
    157 350
    158 277
    159 388
    160 347
    161 288
    162 372
    163 250
    164 308
    165 307
    166 318
    167 303
    168 240
    169 246
    170 299
    171 291
    172 284
    173 278
    174 273
    175 384
    176 120
    177  215*
    178 262
    179 249
    180 231
    181 322
    182 249
    183 249
    184 243
    185   234***
    186 255
    187 230
    188 108
    189 350
    190 167
    191 216
    192 167
    193 243
    194 205
    195 249
    196 169
    197 244
    198 187
    199 228
    200 180
    201 225
    202 174
    203 136
    204 165
    205 222
    206 160
    207 297
    208 285
    209 137
    210 134
    211 248
    212 116
    213 144
    214 138
    215 132
    216  88
    217 116
    218  73
    219  71
    220 148
    221  81
    222  41
    223 176
    224 222
    225 138
    226 182
    227 188
    228 140
    229 424
    230 244
    231 239
    232 247
    233  202*
    *@3.3 uM
    **@0.3 uM
    ***@30 uM

Claims (16)

What is claimed is:
1. A compound, or salt thereof, of formula (I):
Figure US20160108025A1-20160421-C00313
wherein
R1 is selected from: CO2H or tetrazole and R2 is selected from: H, halo, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl, or R1 is H and R2 is CO2H or tetrazole;
X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, NR8R9, halo-substituted(C1-C4)alkyl, phenyl or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said phenyl or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl, hydroxy-substituted(C1-C4)alkyl, (C1-C4)alkylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl;
R8 is selected from: H, or (C1-C4)alkyl;
R9 is selected from: H, or (C1-C4)alkyl;
R3 is
Figure US20160108025A1-20160421-C00314
where R3a is selected from: H, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl;
R3b is selected from: H, (C1-C4)alkyl or taken together with R3a forms a 3 to 7 membered saturated cycloalkyl or a 3 to 7 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N;
R3c is selected from: H or CH3;
R3d is selected from: H or CH3;
R4 is selected from:
Figure US20160108025A1-20160421-C00315
wherein the dotted line indicates the point of attachment;
R5 is selected from: H or CH3;
R6 is independently selected from: halo, nitrile, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, nitrile-substituted(C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkoxy, nitrile-substituted(C1-C4)alkoxy, (C1-C4)alkylene, N-acetyl, trifluouroacetyl, (C1-C4)alkylthio, halo-substituted thio, halo-substituted (C1-C4)alkylthio, (C3-C6)cycloalkyl, methylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl, halo-substituted(C1-C4) hydroxyalkyl, a 4 to 6 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N, or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said heterocycle or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkyl, halo, hydroxyl, amino or (C1-C4)alkoxy;
R7 is selected from: H or halo;
n is 1, 2 or 3;
m is 0, 1 or 2;
or R3c and R4 taken together with the amine to which R3c and R4 are attached forms a fully saturated 4 to 7 membered heterocycle, where 1 to 2 of the ring carbons are each independently optionally replaced with a N or O, and said heterocycle is optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, hydroxy(C1-C4)alkyl, cyclopropyl or oxo or a pharmaceutically acceptable salt thereof.
2. A compound, or salt thereof, according to claim 1, wherein
R1 is selected from: CO2H, or tetrazole;
R2 is selected from: H, halo, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl;
X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, NR8R9, halo-substituted(C1-C4)alkyl, phenyl or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said phenyl or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl, hydroxy-substituted(C1-C4)alkyl, (C1-C4)alkylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl;
R8 is selected from: H, or (C1-C4)alkyl;
R9 is selected from: H, or (C1-C4)alkyl;
R3 is
Figure US20160108025A1-20160421-C00316
where R3a is selected from: H, (C1-C4)alkyl or halo-substituted(C1-C4)alkyl;
R3b is selected from: H, (C1-C4)alkyl or taken together with R3a forms a 3 to 7 membered saturated cycloalkyl or a 3 to 7 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N;
R3c is selected from: H or CH3;
R3d is selected from: H or CH3;
R4 is selected from:
Figure US20160108025A1-20160421-C00317
wherein the dotted line indicates the point of attachment;
R5 is selected from: H or CH3;
R6 is independently selected from: halo, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkoxy, nitrile-substituted(C1-C4)alkoxy, (C1-C4)alkylene, N-acetyl, trifluouroacetyl, (C1-C4)alkylthio, halo-substituted thio, halo-substituted (C1-C4)alkylthio, (C3-C6)cycloalkyl, methylamino-substituted(C1-C4)alkyl, dimethylamino-substituted(C1-C4)alkyl, halo-substituted(C1-C4) hydroxyalkyl, a 4 to 6 membered saturated heterocycle containing 1 to 2 heteroatoms selected from O, S or N, or a 5 to 6 membered heteroaryl containing 1 to 3 heteroatoms each independently selected from O, N, or S, where said heterocycle or heteroaryl are optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkyl, halo, hydroxyl, amino or (C1-C4)alkoxy;
R7 is selected from: H or halo;
n is 1, 2 or 3;
m is 0, 1, 2, 3 or 4;
or R3c and R4 taken together with the amine to which R3c and R4 are attached forms a fully saturated 4 to 7 membered heterocycle, where 1 to 2 of the ring carbons are each independently optionally replaced with a N or O, and said heterocycle is optionally substituted with 1 to 2 substituents each independently selected from (C1-C4)alkoxy, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, hydroxy(C1-C4)alkyl, cyclopropyl or oxo or a pharmaceutically acceptable salt thereof.
3. The compound of claim 1, or a salt thereof, wherein the compound is of formula (II):
Figure US20160108025A1-20160421-C00318
4. The compound of claim 1, or a salt thereof, wherein the compound is of formula (III):
Figure US20160108025A1-20160421-C00319
5. The compound of claim 1, or a salt thereof, wherein the compound is of formula (IV):
Figure US20160108025A1-20160421-C00320
6. The compound of claim 1, or a salt thereof, wherein the compound is of formula (V):
Figure US20160108025A1-20160421-C00321
7. The compound of claim 1, or a salt thereof, wherein the compound is of formula (VI):
Figure US20160108025A1-20160421-C00322
wherein,
R2 is selected from: H, CH3 or CF3;
X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl;
R6 is independently selected from: halo, (C1-C4)alkyl, halo-substituted(C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkoxy; or a pharmaceutically acceptable salt thereof
8. The compound of claim 1, or a salt thereof, wherein the compound is of formula (VII):
Figure US20160108025A1-20160421-C00323
9. The compound of claim 1, or a salt thereof, wherein the compound is of formula (VIII):
Figure US20160108025A1-20160421-C00324
10. The compound of claim 1, or a salt thereof, wherein the compound is of formula (IX):
Figure US20160108025A1-20160421-C00325
11. The compound, or salt thereof, of claim 1, wherein X is selected from: H, halo, (C1-C4)alkyl, (C1-C4)alkoxy, halo-substituted(C1-C4)alkyl;
R3b is H; or a pharmaceutically acceptable salt thereof.
12. The compound of claim 1, or a salt thereof, wherein the compound is selected from:
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-5-fluoro-4-methoxyaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-ethoxy-5-fluoroaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-dibromo-4-(difluoromethoxy)aniline;
3,5-dichloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxyaniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-((trifluoromethyl)thio)aniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(trifluoromethoxy)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(prop-1-en-2-yl)-4-(trifluoromethoxy)aniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
4-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethoxy)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
3,4,5-trichloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(difluoromethoxy)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4,5-trichloroaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-4-(trifluoromethoxy)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-((trifluoromethyl)thio)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(methylthio)-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(methylthio)aniline;
2-(4-(((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
1-(4-(((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)phenyl)-2,2,2-trifluoroethanone;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-chloroaniline;
3-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4,5-difluoroaniline;
3-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-bromo-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-propylaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-(trifluoromethoxy)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(2,2,2-trifluoroethoxy)aniline;
5-(6-((2-(3,4,5-trichlorophenyl)hydrazinyl)methyl)benzofuran-2-yl)-2H-tetrazole;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-bromo-3-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3,5-dichloro-4-ethoxyaniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-fluoro-4-(trifluoromethoxy)aniline;
N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
3-bromo-N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(2,2,2-trifluoroethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromoaniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
N-((2-(1H-tetrazol-5-yl)-3-(trifluoromethyl)benzofuran-6-yl)methyl)-3-chloro-4-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4,5-trimethoxyaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-chloro-3-propylaniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-5-methyl-4-propylaniline;
3-chloro-N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-((trifluoromethyl)thio)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-4-propylaniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-fluoro-3-(trifluoromethoxy)aniline;
N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3,4,5-trichloroaniline;
N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-((trifluoromethyl)thio)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-chloro-5-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethoxy)aniline;
N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-(trifluoromethoxy)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-ethyl-3-(trifluoromethyl)aniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-fluoro-4-propylaniline;
N-((2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-methyl-4-propylaniline;
N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-4-propyl-3-(trifluoromethyl)aniline;
N-((3-methyl-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-2,2-difluorobenzo[d][1,3]dioxol-5-amine;
N-(1-(2-(1H-tetrazol-5-yl)benzofuran-5-yl)ethyl)-3-chloro-4-propylaniline;
6-(((3,4,5-tribromophenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((2,2-difluorobenzo[d][1,3]dioxol-5-yl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-(trifluoromethyl)-4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-(trifluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-(methylthio)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-(methylthio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-bromo-4-morpholinophenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-(pentafluorothio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-ethyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3,4-bis(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-methyl-4-(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-(2,2,2-trifluoroacetyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3,4-bis(trifluoromethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-bromo-4,5-difluorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-3-(trifluoromethyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-(2,2,2-trifluoroethoxy)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-morpholinophenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-fluoro-5-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)-3-(trifluoromethyl)benzofuran-2-carboxylic acid;
6-(((5-(trifluoromethyl)pyridin-2-yl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-((trifluoromethyl)thio)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((2-methylbenzo[d]thiazol-5-yl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-methoxyphenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3,5-bis(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-methoxy-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((2,6-dichloropyridin-4-yl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((3-chloro-4-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((4-propyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((3,4-dichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((4-ethyl-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((3-propyl-4-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-(((4-chloro-3-propylphenyl)amino)methyl)benzofuran-2-carboxylic acid;
N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-propyl-3-(trifluoromethyl)aniline;
3,4-dichloro-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)aniline;
N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
3-bromo-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
4-(difluoromethoxy)-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-(trifluoromethyl)aniline;
4-bromo-N-((6-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
3-bromo-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
4-bromo-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
3-chloro-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethyl)aniline;
3,4-dichloro-N-((6-chloro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)aniline;
3-bromo-N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
4-(difluoromethoxy)-N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-(trifluoromethyl)aniline
N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
4-bromo-N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
N-((4-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
4-(difluoromethoxy)-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-(trifluoromethyl)aniline;
N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
3-bromo-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-5-yl)methyl)-4-(trifluoromethoxy)aniline;
4-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
4-bromo-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
4-(difluoromethoxy)-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
N-((5-methoxy-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
2-(4-(((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2-difluoroethoxy)-3-(trifluoromethyl)aniline;
N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,4-bis(trifluoromethyl)aniline;
4-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
3-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropylaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-5-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline;
4-ethoxy-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
4-(2,2-difluoroethoxy)-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
4-(difluoromethoxy)-N-((5-methoxy-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
4-(difluoromethoxy)-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
N-((5-methyl-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-ethoxyaniline;
N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropoxy-3-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-methoxyaniline;
N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
4-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-(trifluoromethyl)aniline;
3-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
N-((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
6-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-5-(trifluoromethyl)pyridin-3-amine;
3-bromo-4-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
3-bromo-4-ethyl-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-chloroaniline;
3-bromo-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)-3-(trifluoromethyl)aniline;
3,5-dibromo-4-(difluoromethoxy)-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
3-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)aniline;
7-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2-methylbenzofuran-5-amine;
4-bromo-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3,5-bis(trifluoromethyl)aniline;
3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-propylaniline;
N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)-3-(trifluoromethyl)aniline;
3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
3-bromo-N-((7-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethoxy)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-7-chloro-2-methylbenzofuran-5-amine;
N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-5-(trifluoromethyl)aniline;
3-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
2-(difluoromethoxy)-5-(((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)benzonitrile;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(difluoromethoxy)aniline;
5-(((5-bromo-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(difluoromethoxy)benzonitrile;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-5-(trifluoromethyl)aniline;
5-(((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(difluoromethoxy)benzonitrile;
3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(trifluoromethyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-6-chloro-5-(trifluoromethyl)pyridin-3-amine;
3-chloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-(2,2,2-trifluoroethoxy)aniline;
N-((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxy-3-(trifluoromethyl)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-isopropyl-3-(trifluoromethyl)aniline;
3,4-dichloro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl benzo[d]isothiazol-5-amine;
2-(4-(((7-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-2-(trifluoromethyl)phenoxy)acetonitrile;
3-chloro-4-ethoxy-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-5-(trifluoromethoxy)aniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-methyl-5-(trifluoromethyl)aniline;
4-chloro-3-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
3-chloro-4-fluoro-N-((5-fluoro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-isobutoxyaniline;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-ethoxyaniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2-fluoro-4-(trifluoromethoxy)aniline;
N-((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-2,2,4,4-tetrafluoro-4H-benzo[d][1,3]dioxin-6-amine;
3-chloro-N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-5-methyl-4-propylaniline;
N-((5-chloro-2-(1H-tetrazol-5-yl)benzofuran-6-yl)methyl)-4-fluoro-3-(2,2,2-trifluoroethyl)aniline;
N, N-bis((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-isobutoxyaniline;
7-(((2-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)amino)-4-(trifluoromethyl)-2H-chromen-2-one;
5-chloro-6-(((4-(difluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-chloro-6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
6-(((3-chloro-4-(2,2,2-trifluoroethoxy)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
6-(((3-chloro-4-(trifluoromethoxy)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
6-(((3-bromo-4-(trifluoromethoxy)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
6-(((3-chloro-4-((trifluoromethyl)thio)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
6-(((4-bromo-3,5-bis(trifluoromethyl)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
6-(((4-(difluoromethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)-5-fluorobenzofuran-2-carboxylic acid;
5-fluoro-6-(((4-(2,2,2-trifluoroethoxy)-3-(trifluoromethyl)phenyl)amino)methyl)benzofuran-2-carboxylic acid;
5-fluoro-6-(((3,4,5-trichlorophenyl)amino)methyl)benzofuran-2-carboxylic acid; and
N-((3-(2H-tetrazol-5-yl)benzofuran-6-yl)methyl)-3-bromo-4-(trifluoromethoxy)aniline.
13. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1, or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable carriers.
14. A combination comprising a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof and one or more therapeutically active co-agents.
15. A method to treat, prevent or ameliorate a hERG related condition, comprising administering to a subject in need thereof an effective amount of a compound, or salt thereof, of claim 1.
16. The method of claim 15, wherein the hERG related condition is selected from LQT syndrome, GOF syndrome, Na syndrome, Jervell syndrome and Lange-Nielsen syndrome.
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