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US20170173016A1 - Heterocyclic compounds and their use for the treatment of neurodegenerative tauopathies - Google Patents

Heterocyclic compounds and their use for the treatment of neurodegenerative tauopathies Download PDF

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US20170173016A1
US20170173016A1 US15/451,475 US201715451475A US2017173016A1 US 20170173016 A1 US20170173016 A1 US 20170173016A1 US 201715451475 A US201715451475 A US 201715451475A US 2017173016 A1 US2017173016 A1 US 2017173016A1
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trifluorophenyl
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Carlo Ballatore
Kurt R. Brunden
Adam T. Hoye
Virginia M.Y. Lee
Amos B. Smith, III
John Q. Trojanowski
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University of Pennsylvania Penn
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    • A—HUMAN NECESSITIES
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    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic 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
    • A61K31/41—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
    • A61K31/4196—1,2,4-Triazoles
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • 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
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic 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
    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • 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
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs

Definitions

  • the invention is directed to compounds and methods for the treatment of neurodegenerative tauopathies such as Alzheimer's disease and frontotemporal lobar degeneration.
  • Neurodegenerative tauopathies including Alzheimer's disease (AD), are characterized by the misfolding and aggregation of the microtubule (MT)-associated protein tau. Normally, tau binds to and stabilizes MTs, thereby maintaining the network of MTs essential for axonal transport in neurons. In AD, tau becomes sequestered into aggregates, known as neurofibrillary tangles (NFTs) and neuropil threads, resulting in reduced MT-binding. This loss of tau function is believed to lead to MT destabilization and consequent axonal transport deficits, which could result in neuronal dysfunction and death.
  • NFTs neurofibrillary tangles
  • MT function may be compromised
  • frontotemporal lobar degeneration multiple sclerosis, Parkinson's disease, amyotrophic laterial sclerosis, schizophrenia, Huntington's disease, multiple sclerosis, and traumatic brain injury (TBI), especially repetitive TBI (rTBI) such as that due to dementia pugilistica and recurrent football concussions and military closed head injuries, which also is known as chronic traumatic encephalopathy (CTE).
  • CTE chronic traumatic encephalopathy
  • Compounds that can cross the blood brain barrier and effectively stabilize MT are needed in order to treat neurodegenerative diseases caused, at least in part, by misfolding and aggregation of the MT-associated protein tau.
  • Triazolopyrimidine compounds of formula I Triazolopyrimidine compounds of formula I, phenylpyrimidine compounds of formula II, pyridopyridazine and pyridotriazine compounds of formula III, and pyridazine compounds of formula IV, as described herein, are described as being useful for the treatment of neurodegenerative diseases.
  • FIG. 1 depicts MT-stabilization assay (acetyl tubulin, “AcTub”) results of embodiments of the invention in HEK/QBI 293 cells.
  • FIG. 2 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51549).
  • FIG. 3 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51552).
  • FIG. 4 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51554).
  • FIG. 5 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51555).
  • FIG. 6 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51556).
  • FIG. 7 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51557).
  • FIG. 8 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51561).
  • FIG. 9 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51562).
  • FIG. 10 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51565).
  • FIG. 11 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51563).
  • FIG. 12 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51564).
  • FIGS. 13A and 13B depicts pharmacokinetic testing of CNDR-51549 (13A) and CNDR-51555 (13B), demonstrating that both compounds have brain exposure.
  • FIG. 14 depicts CNDR-51549 administration at 1 mg/kg daily to wild-type mice. This administration results in an increase in the fraction of brain ⁇ -tubulin that is acetylated (AcTub).
  • microtubule-stabilizing compounds will be useful in treating neurodegenerative diseases, in particular, tauopathies, for example, Alzheimer's disease, frontotemporal lobar degeneration, Pick's disease, progressive supranuclear palsy (PSP), and corticobasal degeneration.
  • tauopathies for example, Alzheimer's disease, frontotemporal lobar degeneration, Pick's disease, progressive supranuclear palsy (PSP), and corticobasal degeneration.
  • the compounds of the invention may be useful for other diseases where tau pathology is a co-morbidity or where microtubule function is compromised, for example, schizophrenia, Parkinson's disease (PD), PD with dementia, Lewy body disease with dementia, and amyotrophic lateral sclerosis.
  • the compounds of the invention can also be used to treat traumatic brain injury (TBI), especially repetitive TBI (rTBI), such as that due to dementia pugilistica and recurrent football concussions and military closed head injuries such as that due to IEDs, which also is known as chronic traumatic encephalopathy (CTE), with features of tauopathy or AD-like pathology. It is speculated that CTE also may emerge from PTSD.
  • TBI traumatic brain injury
  • rTBI repetitive TBI
  • IEDs which also is known as chronic traumatic encephalopathy
  • CTE chronic traumatic encephalopathy
  • These classes of compounds include triazolopyrimidine compounds of formula I and phenylpyrimidine compounds of formula II, as described herein.
  • Other classes of compounds for use in the invention include pyridopyridazine and pyridotriazine compounds of formula III and pyridazine compounds of formula IV, as described herein.
  • Phenylpyrimidine compounds for use in the invention include those of formula I:
  • Stereoisomeric forms of the compounds of formula I for example, enantiomers, diastereomers, and atropisomers, are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula I.
  • Particularly preferred compounds of formula I include those wherein R 1 is Cl. In other embodiments, R 1 is H. In yet others, R 1 is F. In still other embodiments, R 1 is Br.
  • R 3 is H.
  • R 2 is C 1-6 alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl.
  • R 3 is substituted C 1-6 alkyl, wherein the alkyl is substituted with, for example halogen or trihaloalkyl such as trifluoromethyl.
  • R 2 is preferably —CH(CH 3 )CF 3 , and all stereoisomers thereof, or —CH 2 CF 3 .
  • R 2 and R 3 together with the N atom to which they are attached, form a heterocycloC 3-6 alkyl, for example, a piperdinyl, piperazinyl, or morpholinyl.
  • Such heterocycloC 3-6 alkyls can also be optionally substituted with, for example, one or more C 1-6 alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl.
  • R 4 is H, Cl, F, or Br. In some embodiments, R 4 is H. In other embodiments, R 4 is Cl. In yet other embodiments, R 4 is F. In yet other embodiments, R 4 is Br.
  • R 5 is H, Cl, F, or Br. In some embodiments, R 5 is H. In other embodiments, R 5 is Cl. In yet other embodiments, R 5 is F. In yet other embodiments, R 5 is Br.
  • Particularly preferred compounds include those wherein R 4 and R 5 are each F.
  • R 6 is F, Cl, Br, —OC 1-6 alkyl; or —OC 1-6 alkyleneNR 7 R 8 , wherein R 7 and R 8 are each independently H or C 1-6 alkyl. R 7 and R 8 can be the same or different.
  • R 6 is F.
  • R 6 is Cl.
  • R 6 is Br.
  • R 6 is —N 3 .
  • R 6 is —OC 1-6 alkyl, wherein the C 1-6 alkyl is, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl.
  • R 6 is —OC 1-6 alkyleneNR 7 R 8 , wherein R 7 and R 8 are each independently H or C 1-6 alkyl, for example, methyl, ethyl, propyl, and the like.
  • Preferred alkylene moieties include those having 1, 2, 3, 4, 5, or 6 carbon atoms.
  • Particularly preferred compounds are those wherein R 6 is —O—CH 2 CH 2 CH 2 —N(CH 3 ) 2 .
  • R 6 is —O—CH 2 CH 2 CH 2 —NH(CH 3 ).
  • R 4 , R 5 , and R 6 are each F.
  • R 9 is pyridinyl, preferably 2-pyridinyl, pyrazinyl, preferably 2-pyrazinyl, or pyrazolyl, preferably 1-pyrazolyl, any of which can be substituted with one or more of F, Cl, Br, or C 1-6 alkyl, for example, methyl, ethyl, propyl, butyl, and the like.
  • R9 is pyrimidyl, imidazolyl, pyrrolyl, quinolinyl, isoquinolinyl, thienyl, or furyl, any of which can be substituted with one or more of F, Cl, Br, or C 1-6 alkyl, for example, methyl, ethyl, propyl, butyl, and the like.
  • Particularly preferred compounds of formula I include, for example, the compounds set forth in the following Table 1:
  • Triazolopyrimidine compounds for use in the invention include those of formula II:
  • Stereoisomeric forms of the compounds of formula II are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula II.
  • Preferred compounds of formula II include those wherein R 1 is Cl. Other preferred compounds of formula II include those wherein R 1 is H. Other preferred compounds of formula II include those wherein R 1 is F. Other preferred compounds of formula II include those wherein R 1 is Br.
  • Exemplary compound of formula II include those wherein R 2 is C 1-6 alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl. Also preferred are compounds of formula II wherein R 2 is substituted C 1-6 alkyl, wherein the alkyl is substituted with halogen or trihaloalkyl such as trifluoromethyl.
  • R 2 is preferably —CH(CH 3 )(CF 3 ), and all stereoisomers thereof, and —CH 2 (CF 3 ).
  • R 2 and R 3 together with the nitrogen atom to which they are attached, form a heterocycloC 3-6 alkyl, such as, for example, morpholinyl, piperidinyl, and piperazinyl.
  • R 3 is H.
  • R 4 is H. Preferably R 4 is F. In other embodiments, R 4 is Cl. In other embodiments, R 4 is Br.
  • R 5 is H. Preferably R 5 is F. In other embodiments, R 5 is Cl. In other embodiments, R 5 is Br.
  • R 3 , R 4 , and R 5 are each F.
  • R 6 is F
  • R 6 is Cl
  • R 6 is Br
  • R 6 is —N 3
  • R 6 is H
  • R 6 is F when R 3 , R 4 , and R 5 are each F.
  • R 6 is —OC 1-6 alkyl wherein preferred alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and t-butyl.
  • R 6 is —OC 1-6 alkyleneOH wherein the C 1-6 alkylene includes 1, 2, 3, 4, 5, or 6 carbons.
  • the alkylene is —CH 2 CH 2 CH 2 —.
  • R 6 is —OC 1-6 alkylene-halo wherein the C 1-6 alkylene includes 1, 2, 3, 4, 5, or 6 carbons.
  • the alkylene is —CH 2 CH 2 CH 2 — and the halo is preferably F or Cl.
  • R 6 is —OC 1-6 alkyleneNR 7 R 8 , wherein the C 1-6 alkylene wherein the C 1-6 alkylene includes 1, 2, 3, 4, 5, or 6 carbons.
  • the alkylene is —CH 2 CH 2 CH 2 —.
  • —OC 1-6 alkyleneNR 7 R 8 include, for example, —O—CH 2 CH 2 CH 2 —N(CH 3 ) 2 or —O—CH 2 CH 2 CH 2 —NH(CH 3 ). It is particularly preferred that R 6 is —OC 1-6 alkyleneNR 7 R 8 when R 3 , R 4 , and R 5 are each F.
  • R 6 is —OC 1-6 substituted-alkyleneNR 7 R 8 , wherein the C 1-6 alkylene includes 1, 2, 3, 4, 5, or 6 carbons.
  • the alkylene is a C 3 alkylene.
  • Preferred substitutents include halogen, C 1-6 alkyl, and heterocycloalkyl.
  • R 7 and R 8 can be the same or different.
  • R 7 and R 8 are independently H or methyl.
  • Particularly preferred embodiments of —OC 1-6 substituted-alkyleneNR 7 R 8 include, for example, —O—CH 2 CH 2 CH(oxetanyl)-N(CH 3 ) 2 or —O—CH 2 CH 2 CH 2 —NH(CH 3 ). It is particularly preferred that R 6 is —OC 1-6 substituted-alkyleneNR 7 R 8 when R 3 , R 4 , and R 5 are each F.
  • R 7 and R 8 can be the same or different.
  • R 7 and R 8 can each be independently H, C 1-6 alkyl, substituted C 1-6 alkyl, —C(O)C 1-6 alkyl, or aryl; or R 7 and R 8 together form a heterocyclic ring.
  • R 7 and R 8 are independently H or C 1-6 alkyl.
  • R 7 is H and R 8 is C 1-6 alkyl.
  • R 7 is H and R 8 is substituted C 1-6 alkyl.
  • Preferred substituents include trihaloalkyl such as trifluoromethyl.
  • R 7 is H and R 8 is —C(O)C 1-6 alkyl, wherein preferred alkyl groups are methyl, ethyl, propyl, isopropyl, sec-butyl, and tert-butyl.
  • R 7 is H and R 8 is aryl, for example phenyl or naphthyl.
  • R 7 and R 8 together form a heterocyclic ring such as morpholinyl, piperidinyl, and piperazinyl.
  • R 7 and R 8 are independently H or methyl.
  • the C 3-6 cycloalkylene is cyclopropylene or cyclobutylene, preferably, cyclobutylene.
  • R 6 is —OC 3-6 cycloalkyleneNR 7 R 8 when R 3 , R 4 , and R 5 are each F.
  • Preferred compounds of formula II include, for example, those compounds set forth in Table 2 below:
  • Pyridopyridazine and pyridotriazine compounds for use in the invention include those of formula III:
  • Stereoisomeric forms of the compounds of formula III are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula III.
  • Preferred embodiments of compounds of formula III are those wherein X is CH. Other embodiments include those compounds of formula III wherein X is N.
  • R 1 is C 1-6 alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl.
  • R 1 is substituted C 1-6 alkyl.
  • substituents include, for example, halogen or trihalo alkyl such as —CF 3 .
  • Preferred substituted C 1-6 alkyl include —CH(CH 3 )CF 3 , and all stereoisomers thereof, and —CH 2 CF 3 .
  • Particularly preferred compounds of formula III for use in the invention are those wherein R 2 is Cl or F, preferably Cl.
  • R 3 is F. In other embodiments, R 3 is Cl. In yet other embodiments, R 3 is Br.
  • R 4 is F. In other embodiments, R 4 is Cl. In yet other embodiments, R 4 is Br.
  • R 5 is F. In other embodiments, R 5 is Cl. In yet other embodiments, R 5 is Br.
  • R 3 , R 4 , and R 5 are F.
  • each of R 3 , R 4 , and R 5 is F.
  • Preferred compounds of formula III include
  • Pyridazine compounds for use in the invention include those of formula IV:
  • Stereoisomeric forms of the compounds of formula IV are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula IV.
  • Particularly preferred compounds of formula IV for use in the invention are those wherein R 1 is methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl, preferably methyl. Also preferred are those compounds wherein R 2 is Cl. Other preferred compounds of formula IV are those wherein R 2 is F. In other preferred compounds of formula IV, R 2 is Br.
  • Preferred embodiments of the invention include those compounds of formula IV wherein R 3 is phenyl. Particularly preferred are embodiments wherein R 3 is phenyl substituted with halo such as Cl. In other embodiments, R 3 is thienyl, preferably thienyl substituted with halo such as chloro.
  • R 4 is F. In other embodiments, R 4 is Cl. In yet other embodiments, R 4 is Br.
  • R 5 is F. In other embodiments, R 5 is Cl. In yet other embodiments, R 5 is Br.
  • R 6 is F. In other embodiments, R 6 is Cl. In yet other embodiments, R 6 is Br.
  • R 4 , R 5 , and R 6 are F.
  • each of R 4 , R 5 , and R 6 is F.
  • C 1-6 alkyl refers to straight or branched aliphatic groups having from 1 to 6 carbon atoms. Examples include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, isopentyl, hexyl, and the like.
  • C 1-6 alkylene refers to straight or branched aliphatic groups having from 1 to 6 carbon atoms and having two points of attachment, for example, methylene (—CH 2 —), ethylene (—CH 2 —CH 2 —), propylene (—CH 2 —CH 2 —CH 2 —), and the like.
  • substituted C 1-6 alkyl refers to C 1-6 alkyl groups as defined herein, substituted with another moiety that is, for example, F, Cl, Br, CF 3 , or heterocycloalkyl.
  • C 3-6 cycloalkyl refers to a cyclic aliphatic group having from 3 to 6 carbon atoms. Examples include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
  • C 3-6 cycloalkylene refers to a cyclic aliphatic group having from 3 to 6 carbon atoms and having two points of attachment, for example, cyclopropylene, cyclobutylene, cyclopentylene, and cyclohexylene.
  • halo or halogen refers to F, Cl, Br, or I.
  • heterocycloC 3-6 alkyl or “heterocycloalkyl” refers to an aliphatic cyclic moiety that includes from 3-6 carbon atoms, in addition to 1, 2 or 3 heteroatoms that are N, O, or S.
  • stereoisomers refers to all enantiomerically/diastereomerically pure and enantiomerically/diastereomerically enriched compounds of the invention.
  • Atropisomers that is, stereoisomers resulting from hindered rotation about single bonds, are also within the scope of the term, “stereoisomers.”
  • “pharmaceutically acceptable salt” refers to a salt of a compound of the invention that is generally considered safe for pharmaceutical use. Examples include, for example, hydrochloric acid, sulfuric, fumaric, succinic, ascorbic, maleic, methanesulfonic, and isoethonic acid salts.
  • Phenylpyrimidine compounds within the scope of formula I that can be made according to the procedures set forth in Scheme 1 include, for example, those of Table 3.
  • Triazolopyrimidine compounds of formula II that can be prepared according to the procedures set forth in Scheme 2 include, for example, those set forth in Table 4.
  • MT-stabilizing properties of triazolopyrimidines was investigated in a cell-free MT-polymerization assay, as well in a cell-based assay (HEK/QBI 293 cells) that measures changes in acetyl-tubulin (AcTub), a biomarker of stable MTs.
  • HEK/QBI 293 cells HEK/QBI 293 cells
  • AcTub acetyl-tubulin
  • MT structure in HEK/QBI293 cells as determined by AcTub immunofluo-rescence was examined after 4 h of incubation with cevipabulin.
  • Cells that were treated with 100 nM cevipabulin (8) revealed a large increase in highly organized, AcTub-positive MTs relative to control cells, with the intensity of staining exceeding that observed with 100 nM of the known MT-stabilizing agent, epothilone D (epoD).
  • the MT-destabilizing agent, colchicine led to a significant loss of AcTub staining (data not shown).
  • MT-stabilizing properties of additional triazolopyrimidines, phenylpyrimidines, and pyridazines was investigated in a cell-free MT-polymerization assay, as well in the aforementioned cell-based assay (HEK/QBI 293 cells) that measures changes in acetyl-tubulin (AcTub), a biomarker of stable MTs (Laferriere, N.; MacRae, T.; Brown, D. Tubulin synthesis and assembly in differentiating neurons. Biochemistry and Cell Biology 1997, 75, 103-117; Black, M.; Baas, P.; Humphries, S. Dynamics of alpha-tubulin deacetylation in intact neurons.
  • MT-stabilizing compounds For utility in neurodegenerative diseases, MT-stabilizing compounds must cross the blood-brain barrier (BBB) and enter the brain.
  • BBB blood-brain barrier
  • Table 7 a number of examples show concentrations in the brain that exceed 0.5 ⁇ M an hour after administration of a 5 mg/kg dose, with brain-to-plasma concentration ratios of ⁇ 0.3 or higher.
  • the relative brain exposures predicted by the one hour analysis of brain and plasma compound levels were confirmed by more complete pharmacokinetic analyses, as exemplified by the profiles of CNDR-51549 and CNDR-51555 shown in FIG. 13 .
  • MT-stabilizing agents including cevepabulin, which do not cross the BBB
  • multiple phenylpyrimidine and triazolopyrimidine examples were unexpectedly found to be brain-penetrant.
  • CNDR-51549 was found to cause an increase of AcTub levels in the brains of wild-type mice 3 days after receiving a once-daily 1 mg/kg dose, as shown in FIG. 14 .
  • the compounds of formula I can be administered by a variety of methods known to one skilled in the art. Methods of administration include, but are not limited to, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral routes.
  • the compounds may be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and may be administered together with other biologically active agents. Administration can be systemic or local. In addition, it may be desirable to introduce the compounds into the central nervous system by any suitable route, including intraventricular and intrathecal injection.
  • Preparative reverse phase HPLC purification was performed on a Gilson HPLC system equipped with Gilson 333 pumps, a 215 Liquid Handler, 845Z injection module, and UV detector, employing Waters SunFireTM prep C18 OBDTM columns (5 m 19 ⁇ 50 or 19 ⁇ 100 mm). All samples were purified employing a linear gradient from 10% to 90% of acetonitrile in water over 15 minutes and flow rate of 20 mL/min. Unless otherwise stated, all final compounds were found to be >95% as determined by HPLC/MS and NMR.
  • reaction was quenched with NH 4 Cl (sat. aq.) and extracted with ethyl acetate (3 ⁇ ). The combined organic extracts were washed with NaHCO 3 (sat. aq.), brine, dried over Na 2 SO 4 , filtered and concentrated.
  • 2,4,6-Trifluorophenylacetic acid (0.4710 g, 2.48 mmol, 1.00 equiv) was dissolved in CH 2 Cl 2 (4 mL) and two drops of DMF was added.
  • Oxalyl chloride (0.377 g, 0.26 mL, 2.97 mmol, 1.20 equiv) was added dropwise and stirred for 30 minutes at room temperature. The solution was heated to reflux and stirred for 2 h. After cooling to room temperature the crude acid chloride was used directly in the next step without purification.
  • the reaction mixture containing the acid chloride in CH 2 Cl 2 (4 mL) was added dropwise to a solution containing methyl 3-aminopyrazine-2-carboxylate (0.3794 g, 2.48 mmol, 1.00 equiv), pyridine (0.372 g, 0.38 mL, 4.71 mmol, 1.90 equiv), and DMAP (catalytic quantities).
  • the reaction mixture was stirred for 20 h and then diluted with CH 2 Cl 2 (100 mL) and washed with water, 1 N HCl, and brine.
  • the organic layers was dried over Na 2 SO 4 , concentrated under reduced pressure, and purified via silica gel flash chromatography to deliver 0.2362 g (29%) of the title compound as an orange solid.
  • Methyl 3-(2-(2,4,6-trifluorophenyl)acetamido)pyrazine-2-carboxylate (0.2239 g, 0.69 mmol, 1.00 equiv) and anhydrous K 2 CO 3 (0.1903 g, 1.38 mmol, 2.00 equiv) were suspended in DMF (4 mL) and heated to 80° C. for 3 h. After cooling to room temperature the mixture was poured into ice-cold water, acidified to a pH of 3 with 1 N HCl, and extracted with EtOAc (3 ⁇ ).
  • IR v 3411, 3207, 2923, 2853, 1638, 1616 cm ⁇ 1 .
  • the HEK293 cell subclone, QBI293, was maintained in DMEM supplemented with 10% fetal calf or bovine serum, 1% penicillin/streptomycin antibiotic solution and 1% glutamine at 37° C. in 5% CO 2 .
  • Cells were plated into 6-well plates at a density of 800,000 cells/well. Each plate had a well that contained the known microtubule stabilizer, epothilone D or cevipabulin, as a positive control and the remaining wells were used for compound evaluation. Test compounds were added at multiple concentrations to the test wells and incubated for 4 h.
  • ice-cold phosphate-buffered saline PBS
  • 0.2 ml of ice-cold RIPA 0.5% sodium deoxycholate, 0.1% SDS, 1% NP-40, 5 mM EDTA, pH 8.0
  • protease inhibitor mix (1 ⁇ g/ml each of pepstatin, leupeptin, TLCK, TPCK and trypsin inhibitor)
  • 1 mM PMSF and 1 M trichostatin A was added to the wells.
  • the wells were then scraped using a cell scraper and pipetted into 1.5 ml microfuge tubes.
  • the tubes were sonicated with a handheld sonicator at 20 ⁇ on a power setting of 2, followed by centrifugation for 30 min at 15,000 rpm at 4° C. Supernatants were removed and quantified for protein concentration and the acetyl-tubulin levels were determined using an ELISA as described.
  • 384-well plates were coated with 12G10 ⁇ -tubulin antibody (Developmental Studies Hybridoma Bank at the University of Iowa; 10 ⁇ g/ml) in 30 ⁇ l of cold 0.1 M bicarbonate buffer. After overnight incubation at 4° C., the plates were washed with cold PBS, followed by the addition of Block-Ace solution and overnight incubation at 4° C. The blocking solution was removed and 10 ⁇ l of EC buffer (0.02 M sodium phosphate, pH 7.0, 2 mM EDTA, 0.4 M NaCl, 0.2% bovine serum albumin, 0.05% CHAPS, 0.4% BlockAce and 0.05% NaN 3 ) was added to each well.
  • 12G10 ⁇ -tubulin antibody Developmental Studies Hybridoma Bank at the University of Iowa
  • Block-Ace solution overnight incubation at 4° C.
  • the blocking solution was removed and 10 ⁇ l of EC buffer (0.02 M sodium phosphate, pH 7.0, 2 mM ED
  • Cell culture supernatants were diluted in EC buffer to final protein concentrations of 9, 3, 1.5 and 0.5 ⁇ g/30 ⁇ l, and 30 ⁇ l of each were added to wells in duplicate and plates were subsequently sealed. After overnight incubation at 4° C., the plates were aspirated and washed with cold PBS containing 0.05% Tween-20 and 0.05% thimerisol (PBS-Tween buffer), followed by addition of 30 ⁇ l/well of HRP-conjugated acetyl-tubulin antibody (6-11B-1 antibody from Sigma-Aldrich) that was prepared with a Peroxidase Labeling Kit following the manufacturer's instructions that was subsequently diluted 1:1000 in C buffer (0.02 M sodium phosphate, pH 7.0, 2 mM EDTA, 0.4 M NaCl, 1% bovine serum albumin and 0.05% thimerisol).
  • C buffer 0.02 M sodium phosphate, pH 7.0, 2 mM EDTA, 0.4 M NaC
  • the HEK293 cell subclone, QBI293, was plated onto poly-D-lysine-coated glass coverslips at 50,000 cells/ml in DMEM supplemented with 10% fetal calf or bovine serum, 1% penicillin/streptomycin antibiotic solution and 1% glutamine and maintained overnight at 37° C. in 5% CO 2 .
  • DMEM fetal calf or bovine serum
  • penicillin/streptomycin antibiotic solution 1% glutamine
  • glutamine 1% glutamine
  • cells were left untreated or were treated with 100 nM epothilone D, 100 nM CNDR-51533 or 1 ⁇ M colchicine. After an additional 4 h of incubation at 37° C. in 5% CO 2 , cells were washed twice with PBS, and then fixed for 15 min in PBS containing 4% paraformaldehyde.
  • the cells were again washed twice with PBS, and permeabilized with 0.1% Triton X-100 in PBS for 15 min. Following the Triton X-100 treatment, the cells were washed twice in PBS, and treated with PBS containing 3% bovine serum albumin for 1 h. Acetyl-tubulin antibody was subsequently added (1:1000 dilution) and incubated for 1 h. Cells were then washed cells 3 ⁇ 5 min with 0.1% Triton X-100 in PBS, and secondary antibody (goat-anti-mouse labeled with Alexa fluor 488 at 1:1000) was added and allowed to incubate for 1 h.
  • secondary antibody goat-anti-mouse labeled with Alexa fluor 488 at 1:1000
  • Mouse brains were homogenized in 10 mM ammonium acetate, pH 5.7 (1:2; w/v) using a handheld sonic homogenizer.
  • Mouse plasma was obtained from blood that was collected into a 1.5 ml tube containing 0.5M EDTA solution and which was centrifuged for 10 minutes at 4500 g at 4° C. Aliquots (50 ⁇ l) of brain homogenates (50% w/v in 100 mM NH 4 OAC pH 5.75) or plasma were mixed with 0.2 ml of acetonitrile, centrifuged at 15,000 g, and the resulting supernatant was used for subsequent LC-MS/MS analysis.
  • the LC-MS/MS system was comprised of an Aquity UPLC and a TQ MS that was controlled using MassLynx software (Waters Corporation, Milford, Mass., USA). Compounds were detected using multiple reaction monitoring (MRM) of their specific collision-induced ion transitions. Samples were separated on an Aquity BEH C18 column (1.7 m, 2.1 ⁇ 50 mm) at 35° C. Operation was in positive electrospray ionization mode, with mobile phase A of 0.1% (v/v) formic acid, and B of acetonitrile with 0.1% (v/v) formic acid.
  • MRM multiple reaction monitoring
  • Injections of 5 ⁇ l were separated at a flow rate of 0.6 mL/min using a gradient from 5% to 95% B over two minutes, followed by wash and re-equilibration steps.
  • the MS was operated with a desolvation temperature of 450° C. and a source temperature of 150° C. Desolvation and source nitrogen gas flows were 900 L/hr and 50 L/hr, respectively. Source and MS/MS voltages were optimized for each compound using the MassLynx auto tune utility. To account for possible matrix effects on analytes, standard curves were generated for each compound from brain homogenate and plasma samples that had compound added at 24, 240, 2400 and 24000 nM.
  • tissue-derived sample peak areas fell within the linear portion of standard curves that were prepared and analyzed concurrently with the samples.
  • CD1 mice were administered vehicle (DMSO) or CNDR-51549 at multiple doses once per day for 3 days.
  • Whole brain hemispheres were obtained from the mice, which were euthanized using protocols approved by the University of Pennsylvania Institutional Animal Care and Use Committee, and were homogenized and then briefly sonicated with a handheld sonicator in 1:5 (w/v) RIPA-INH buffer.
  • the homogenates were centrifuged at 100,000 ⁇ g for 30 min at 4° C., and the supernatants were collected.
  • the supernatant samples were diluted before protein determination with a BCA assay. These supernatant samples were utilized in the Acetyl-Tubulin ELISA, as described above.

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Abstract

The present invention is directed to triazolopyrimidine, phenylpyrimidine, pyridopyridazine, and pyridotriazine compounds and their use in the treatment of neurodegenerative disorders.

Description

    CROSS REFERENCE TO RELATED APPLICATION
  • This application is a divisional of U.S. application Ser. No. 14/429,101, filed Mar. 18, 2015, which is the National Stage Entry of International Application No. PCT/US2013/060562, filed Sep. 19, 2013, which claims the benefit of U.S. Provisional Application No. 61/702,800, filed Sep. 19, 2012, the entireties of which are incorporated herein by reference.
    • GOVERNMENT RIGHTS
  • This invention was made with government support under Contract No. AG034140 awarded by the National Institutes of Health. The government has certain rights in the invention.
    • TECHNICAL FIELD
  • The invention is directed to compounds and methods for the treatment of neurodegenerative tauopathies such as Alzheimer's disease and frontotemporal lobar degeneration.
    • BACKGROUND
  • Neurodegenerative tauopathies, including Alzheimer's disease (AD), are characterized by the misfolding and aggregation of the microtubule (MT)-associated protein tau. Normally, tau binds to and stabilizes MTs, thereby maintaining the network of MTs essential for axonal transport in neurons. In AD, tau becomes sequestered into aggregates, known as neurofibrillary tangles (NFTs) and neuropil threads, resulting in reduced MT-binding. This loss of tau function is believed to lead to MT destabilization and consequent axonal transport deficits, which could result in neuronal dysfunction and death.
  • Other neurodegenerative diseases where MT function may be compromised include frontotemporal lobar degeneration, multiple sclerosis, Parkinson's disease, amyotrophic laterial sclerosis, schizophrenia, Huntington's disease, multiple sclerosis, and traumatic brain injury (TBI), especially repetitive TBI (rTBI) such as that due to dementia pugilistica and recurrent football concussions and military closed head injuries, which also is known as chronic traumatic encephalopathy (CTE).
  • Compounds that can cross the blood brain barrier and effectively stabilize MT are needed in order to treat neurodegenerative diseases caused, at least in part, by misfolding and aggregation of the MT-associated protein tau.
    • SUMMARY
  • Triazolopyrimidine compounds of formula I, phenylpyrimidine compounds of formula II, pyridopyridazine and pyridotriazine compounds of formula III, and pyridazine compounds of formula IV, as described herein, are described as being useful for the treatment of neurodegenerative diseases.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 depicts MT-stabilization assay (acetyl tubulin, “AcTub”) results of embodiments of the invention in HEK/QBI 293 cells.
  • FIG. 2 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51549).
  • FIG. 3 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51552).
  • FIG. 4 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51554).
  • FIG. 5 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51555).
  • FIG. 6 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51556).
  • FIG. 7 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51557).
  • FIG. 8 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51561).
  • FIG. 9 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51562).
  • FIG. 10 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51565).
  • FIG. 11 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51563).
  • FIG. 12 depicts acetyl-tubulin level in QBI cells after 4 hours of treatment with one preferred compound of the invention (CNDR-51564).
  • FIGS. 13A and 13B depicts pharmacokinetic testing of CNDR-51549 (13A) and CNDR-51555 (13B), demonstrating that both compounds have brain exposure.
  • FIG. 14 depicts CNDR-51549 administration at 1 mg/kg daily to wild-type mice. This administration results in an increase in the fraction of brain α-tubulin that is acetylated (AcTub).
    •  DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS
  • It has now been discovered that certain classes of microtubule-stabilizing compounds will be useful in treating neurodegenerative diseases, in particular, tauopathies, for example, Alzheimer's disease, frontotemporal lobar degeneration, Pick's disease, progressive supranuclear palsy (PSP), and corticobasal degeneration. In addition, the compounds of the invention may be useful for other diseases where tau pathology is a co-morbidity or where microtubule function is compromised, for example, schizophrenia, Parkinson's disease (PD), PD with dementia, Lewy body disease with dementia, and amyotrophic lateral sclerosis.
  • The compounds of the invention can also be used to treat traumatic brain injury (TBI), especially repetitive TBI (rTBI), such as that due to dementia pugilistica and recurrent football concussions and military closed head injuries such as that due to IEDs, which also is known as chronic traumatic encephalopathy (CTE), with features of tauopathy or AD-like pathology. It is speculated that CTE also may emerge from PTSD.
  • These classes of compounds include triazolopyrimidine compounds of formula I and phenylpyrimidine compounds of formula II, as described herein. Other classes of compounds for use in the invention include pyridopyridazine and pyridotriazine compounds of formula III and pyridazine compounds of formula IV, as described herein.
  • Certain of the compounds described herein, that is, compounds of formulas I, II, III, and IV, have been previously studied for their anti-fungal and anti-cancer properties. As described herein, the compounds of formulas I, II, III, and IV are also useful in the treatment of neurodegenerative diseases.
  • Phenylpyrimidine compounds for use in the invention include those of formula I:
  • Figure US20170173016A1-20170622-C00001
      • wherein
      • R1 is H, Cl, F, or Br;
      • R2 is C1-6alkyl or substituted C1-6alkyl;
      • R3 is H; or R2 and R3, together with the N atom to which they are attached, form a heterocycloC2-6alkyl;
      • R4 is H, Cl, F, or Br;
      • R5 is H, Cl, F, or Br;
      • R6 is F, Cl, Br, —N3, —OC1-6alkyl; —OC1-6alkyleneNR7R8, wherein R7 and R8 are each independently H or C1-6alkyl; and
      • R9 is pyridinyl, pyrimidyl, pyrazinyl, imidazolyl, pyrrolyl, pyrazolyl, quinolinyl, isoquinolinyl, thienyl, or furyl, each of which may be optionally substituted with one or more of F, Cl, Br, or C1-6alkyl.
  • Stereoisomeric forms of the compounds of formula I, for example, enantiomers, diastereomers, and atropisomers, are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula I.
  • Particularly preferred compounds of formula I include those wherein R1 is Cl. In other embodiments, R1 is H. In yet others, R1 is F. In still other embodiments, R1 is Br.
  • Preferably, in compounds of formula I, R3 is H. In such embodiments, R2 is C1-6alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl. Also in embodiments wherein R3 is H, R2 is substituted C1-6alkyl, wherein the alkyl is substituted with, for example halogen or trihaloalkyl such as trifluoromethyl. R2 is preferably —CH(CH3)CF3, and all stereoisomers thereof, or —CH2CF3.
  • In alternative embodiments, R2 and R3, together with the N atom to which they are attached, form a heterocycloC3-6alkyl, for example, a piperdinyl, piperazinyl, or morpholinyl. Such heterocycloC3-6alkyls can also be optionally substituted with, for example, one or more C1-6alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl.
  • In the invention, R4 is H, Cl, F, or Br. In some embodiments, R4 is H. In other embodiments, R4 is Cl. In yet other embodiments, R4 is F. In yet other embodiments, R4 is Br.
  • In the invention, R5 is H, Cl, F, or Br. In some embodiments, R5 is H. In other embodiments, R5 is Cl. In yet other embodiments, R5 is F. In yet other embodiments, R5 is Br.
  • Particularly preferred compounds include those wherein R4 and R5 are each F.
  • In the invention, R6 is F, Cl, Br, —OC1-6alkyl; or —OC1-6alkyleneNR7R8, wherein R7 and R8 are each independently H or C1-6alkyl. R7 and R8 can be the same or different. In some preferred embodiments, R6 is F. In some preferred embodiments, R6 is Cl. In some preferred embodiments, R6 is Br. In some embodiments, R6 is —N3. In other embodiments, R6 is —OC1-6alkyl, wherein the C1-6alkyl is, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl. In yet other embodiments, R6 is —OC1-6alkyleneNR7R8, wherein R7 and R8 are each independently H or C1-6alkyl, for example, methyl, ethyl, propyl, and the like. Preferred alkylene moieties include those having 1, 2, 3, 4, 5, or 6 carbon atoms. Particularly preferred compounds are those wherein R6 is —O—CH2CH2CH2—N(CH3)2. In other embodiments, R6 is —O—CH2CH2CH2—NH(CH3).
  • In other preferred compounds of formula I, R4, R5, and R6 are each F.
  • In preferred embodiments, R9 is pyridinyl, preferably 2-pyridinyl, pyrazinyl, preferably 2-pyrazinyl, or pyrazolyl, preferably 1-pyrazolyl, any of which can be substituted with one or more of F, Cl, Br, or C1-6alkyl, for example, methyl, ethyl, propyl, butyl, and the like. In other embodiments, R9 is pyrimidyl, imidazolyl, pyrrolyl, quinolinyl, isoquinolinyl, thienyl, or furyl, any of which can be substituted with one or more of F, Cl, Br, or C1-6alkyl, for example, methyl, ethyl, propyl, butyl, and the like.
  • Particularly preferred compounds of formula I, include, for example, the compounds set forth in the following Table 1:
  • TABLE 1
    Figure US20170173016A1-20170622-C00002
    X R1 R2 R3 R4 R5 R6
    N Cl —CH(CH3)CF3 (S) H F F F
    N Cl —CH(CH3)CF3 (R) H F F F
    N Cl —CH(CH3)CF3 (S,R) H F F F
    N Cl H H F F F
    CH Cl —CH(CH3)CF3 (S) H F F F
    CH Cl —CH(CH3)CF3 (R) H F F F
    CH Cl —CH(CH3)CF3 (S,R) H F F F
    CH Cl H H F F F
    N Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2N(CH3)2
    N Cl —CH(CH3)CF3 (R) H F F —OCH2CH2CH2N(CH3)2
    N Cl —CH(CH3)CF3 (S,R) H F F —OCH2CH2CH2N(CH3)2
    CH Cl H H F F —OCH2CH2CH2N(CH3)2
    CH Cl H H F F —OtBu
    CH Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2N(CH3)2
    CH Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2NH(CH3)
  • Other preferred compounds of formula I include:
  • Figure US20170173016A1-20170622-C00003
  • Triazolopyrimidine compounds for use in the invention include those of formula II:
  • Figure US20170173016A1-20170622-C00004
      • wherein
      • R1 is H, Cl, F, or Br;
      • R2 is C1-6alkyl, or substituted C1-6alkyl;
      • R3 is H; or R2 and R3, together with the N atom to which they are attached, form a heterocycloC3-6alkyl;
      • R4 is H, Cl, F, or Br;
      • R5 is H, Cl, F, or Br;
      • R6 is F, Cl, Br, —N3, —OC1-6alkyl; —OC1-6alkyleneOH; —OC1-6alkylene-halo; —OC1-6alkyleneNR7R8; —OC1-6substituted-alkyleneNR7R8; or
        • —OC3-6cycloalkyleneNR7R8, wherein R7 and R8 are each independently H, C1-6alkyl, substituted C1-6alkyl, —C(O)C1-6alkyl, or aryl; or R7 and R8 together form a heterocyclic ring.
  • Some embodiments of the invention include compounds of formula II wherein
      • R1 is H, Cl, F, or Br;
      • R2 is C1-6alkyl, or substituted C1-6alkyl;
      • R3 is H; or R2 and R3, together with the N atom to which they are attached, form a heterocycloC3-6alkyl;
      • R4 is H, Cl, F, or Br;
      • R5 is H, Cl, F, or Br;
      • R6 is F, Cl, Br, —OC1-6alkyl; —OC1-6alkyleneNR7R8, or —OC3-6cycloalkyleneNR7R8,
        • wherein R7 and R8 are each independently H or C1-6alkyl.
  • Stereoisomeric forms of the compounds of formula II, for example, enantiomers, diastereomers, and atropisomers, are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula II.
  • Preferred compounds of formula II include those wherein R1 is Cl. Other preferred compounds of formula II include those wherein R1 is H. Other preferred compounds of formula II include those wherein R1 is F. Other preferred compounds of formula II include those wherein R1 is Br.
  • Exemplary compound of formula II include those wherein R2 is C1-6alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl. Also preferred are compounds of formula II wherein R2 is substituted C1-6alkyl, wherein the alkyl is substituted with halogen or trihaloalkyl such as trifluoromethyl. For example, R2 is preferably —CH(CH3)(CF3), and all stereoisomers thereof, and —CH2(CF3).
  • In some embodiments, R2 and R3, together with the nitrogen atom to which they are attached, form a heterocycloC3-6alkyl, such as, for example, morpholinyl, piperidinyl, and piperazinyl.
  • In preferred embodiments of compounds of formula II of the invention R3 is H.
  • In some embodiments, R4 is H. Preferably R4 is F. In other embodiments, R4 is Cl. In other embodiments, R4 is Br.
  • In some embodiments, R5 is H. Preferably R5 is F. In other embodiments, R5 is Cl. In other embodiments, R5 is Br.
  • In particularly preferred embodiments of the invention, R3, R4, and R5 are each F.
  • Also preferred are compounds of formula II wherein R6 is F. Other preferred compounds of formula II are those wherein R6 is Cl. Other preferred compounds of formula II are those wherein R6 is Br. IN other embodiments, R6 is —N3. Other preferred compounds of formula II are those wherein R6 is H. It is particularly preferred that R6 is F when R3, R4, and R5 are each F.
  • In some embodiments, R6 is —OC1-6alkyl wherein preferred alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and t-butyl.
  • In yet other embodiment, R6 is —OC1-6alkyleneOH wherein the C1-6alkylene includes 1, 2, 3, 4, 5, or 6 carbons. Preferably, the alkylene is —CH2CH2CH2—.
  • In yet other embodiment, R6 is —OC1-6alkylene-halo wherein the C1-6alkylene includes 1, 2, 3, 4, 5, or 6 carbons. Preferably, the alkylene is —CH2CH2CH2— and the halo is preferably F or Cl.
  • In other preferred embodiments, R6 is —OC1-6alkyleneNR7R8, wherein the C1-6alkylene wherein the C1-6alkylene includes 1, 2, 3, 4, 5, or 6 carbons. Preferably, the alkylene is —CH2CH2CH2—.
  • Particularly preferred embodiments of —OC1-6alkyleneNR7R8 include, for example, —O—CH2CH2CH2—N(CH3)2 or —O—CH2CH2CH2—NH(CH3). It is particularly preferred that R6 is —OC1-6alkyleneNR7R8 when R3, R4, and R5 are each F.
  • In other embodiments, R6 is —OC1-6substituted-alkyleneNR7R8, wherein the C1-6alkylene includes 1, 2, 3, 4, 5, or 6 carbons. Preferably, the alkylene is a C3alkylene. Preferred substitutents include halogen, C1-6alkyl, and heterocycloalkyl. R7 and R8 can be the same or different. Preferably, R7 and R8 are independently H or methyl. Particularly preferred embodiments of —OC1-6substituted-alkyleneNR7R8 include, for example, —O—CH2CH2CH(oxetanyl)-N(CH3)2 or —O—CH2CH2CH2—NH(CH3). It is particularly preferred that R6 is —OC1-6substituted-alkyleneNR7R8 when R3, R4, and R5 are each F.
  • R7 and R8 can be the same or different. R7 and R8 can each be independently H, C1-6alkyl, substituted C1-6alkyl, —C(O)C1-6alkyl, or aryl; or R7 and R8 together form a heterocyclic ring. Preferably, R7 and R8 are independently H or C1-6alkyl. In other embodiments R7 is H and R8 is C1-6alkyl. In other embodiments R7 is H and R8 is substituted C1-6alkyl. Preferred substituents include trihaloalkyl such as trifluoromethyl. In other embodiments R7 is H and R8 is —C(O)C1-6alkyl, wherein preferred alkyl groups are methyl, ethyl, propyl, isopropyl, sec-butyl, and tert-butyl. In yet other embodiments, R7 is H and R8 is aryl, for example phenyl or naphthyl. Alternatively R7 and R8 together form a heterocyclic ring such as morpholinyl, piperidinyl, and piperazinyl. Preferably, R7 and R8 are independently H or methyl.
  • In certain embodiments wherein R6 is —OC3-6cycloalkyleneNR7R8, the C3-6cycloalkylene is cyclopropylene or cyclobutylene, preferably, cyclobutylene.
  • It is particularly preferred that R6 is —OC3-6cycloalkyleneNR7R8 when R3, R4, and R5 are each F.
  • Preferred compounds of formula II include, for example, those compounds set forth in Table 2 below:
  • TABLE 2
    Figure US20170173016A1-20170622-C00005
    R1 R2 R3 R4 R5 R6
    Cl H H F F F
    Cl —CH(CH3)CF3 (S) H F F F
    Cl —CH(CH3)CF3 (R) H F F F
    Cl —CH(CH3)CF3 (S,R) H F F F
    Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2NHCH3
    Cl —CH(CH3)CF3 (R) H F F —OCH2CH2CH2NHCH3
    Cl —CH(CH3)CF3 (S,R) H F F —OCH2CH2CH2NHCH3
    Cl H H F F —OCH2CH2CH2NHCH3
    Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2N(CH3)2
    Cl —CH(CH3)CF3 (R) H F F —OCH2CH2CH2N(CH3)2
    Cl —CH(CH3)CF3 (S,R) H F F —OCH2CH2CH2N(CH3)2
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00006
    Cl —CH(CH3)CF3 (R) H F F
    Figure US20170173016A1-20170622-C00007
    Cl —CH(CH3)CF3 (S,R) H F F
    Figure US20170173016A1-20170622-C00008
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00009
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00010
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00011
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00012
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00013
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00014
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00015
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00016
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00017
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00018
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00019
    Cl —CH(CH3)CF3 (S) H F F
    Figure US20170173016A1-20170622-C00020
  • Pyridopyridazine and pyridotriazine compounds for use in the invention include those of formula III:
  • Figure US20170173016A1-20170622-C00021
      • wherein
      • X is CH or N;
      • R1 is C1-6alkyl or substituted C1-6alkyl;
      • R2 is F, Cl, or Br;
      • R3 is F, Cl, or Br;
      • R4 is F, Cl, or Br; and
      • R5 is F, Cl, or Br.
  • Stereoisomeric forms of the compounds of formula III, for example, enantiomers, diastereomers, and atropisomers, are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula III.
  • Preferred embodiments of compounds of formula III are those wherein X is CH. Other embodiments include those compounds of formula III wherein X is N.
  • Preferably, R1 is C1-6alkyl, for example, methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl. In other embodiments, R1 is substituted C1-6alkyl. Exemplary substituents include, for example, halogen or trihalo alkyl such as —CF3. Preferred substituted C1-6alkyl include —CH(CH3)CF3, and all stereoisomers thereof, and —CH2CF3.
  • Particularly preferred compounds of formula III for use in the invention are those wherein R2 is Cl or F, preferably Cl.
  • In some embodiments, R3 is F. In other embodiments, R3 is Cl. In yet other embodiments, R3 is Br.
  • In some embodiments, R4 is F. In other embodiments, R4 is Cl. In yet other embodiments, R4 is Br.
  • In some embodiments, R5 is F. In other embodiments, R5 is Cl. In yet other embodiments, R5 is Br.
  • Also preferred are compounds of formula III wherein at least one of R3, R4, and R5 is F. In alternative embodiments, each of R3, R4, and R5 is F.
  • Preferred compounds of formula III include
  • Figure US20170173016A1-20170622-C00022
  • Pyridazine compounds for use in the invention include those of formula IV:
  • Figure US20170173016A1-20170622-C00023
      • wherein
      • R1 is C1-6alkyl;
      • R2 is F, Cl, or Br;
      • R3 is phenyl, pyridinyl, pyrimidyl, pyrazinyl, imidazolyl, pyrrolyl, pyrazolyl, quinolunyl, isoquinolinyl, thienyl, or furyl, each of which may be optionally substituted with one or more of F, Cl, or Br;
      • R4 is F, Cl, or Br;
      • R5 is F, Cl, or Br; and
      • R6 is F, Cl, or Br.
  • Stereoisomeric forms of the compounds of formula IV, for example, enantiomers, diastereomers, and atropisomers, are also within the scope of the invention, as are pharmaceutically acceptable salts of any compound or stereoisomer of formula IV.
  • Particularly preferred compounds of formula IV for use in the invention are those wherein R1 is methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, and tert-butyl, preferably methyl. Also preferred are those compounds wherein R2 is Cl. Other preferred compounds of formula IV are those wherein R2 is F. In other preferred compounds of formula IV, R2 is Br.
  • Preferred embodiments of the invention include those compounds of formula IV wherein R3 is phenyl. Particularly preferred are embodiments wherein R3 is phenyl substituted with halo such as Cl. In other embodiments, R3 is thienyl, preferably thienyl substituted with halo such as chloro.
  • In some embodiments, R4 is F. In other embodiments, R4 is Cl. In yet other embodiments, R4 is Br.
  • In some embodiments, R5 is F. In other embodiments, R5 is Cl. In yet other embodiments, R5 is Br.
  • In some embodiments, R6 is F. In other embodiments, R6 is Cl. In yet other embodiments, R6 is Br.
  • Other preferred compounds of formula IV include those wherein at least one of R4, R5, and R6 is F. In yet other embodiments, each of R4, R5, and R6 is F.
  • Preferred compounds of formula IV are
  • Figure US20170173016A1-20170622-C00024
  • As used herein, “C1-6alkyl” refers to straight or branched aliphatic groups having from 1 to 6 carbon atoms. Examples include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, isopentyl, hexyl, and the like. “C1-6alkylene” refers to straight or branched aliphatic groups having from 1 to 6 carbon atoms and having two points of attachment, for example, methylene (—CH2—), ethylene (—CH2—CH2—), propylene (—CH2—CH2—CH2—), and the like.
  • As used herein, “substituted C1-6alkyl” refers to C1-6alkyl groups as defined herein, substituted with another moiety that is, for example, F, Cl, Br, CF3, or heterocycloalkyl.
  • As used herein “C3-6cycloalkyl” refers to a cyclic aliphatic group having from 3 to 6 carbon atoms. Examples include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. “C3-6cycloalkylene” refers to a cyclic aliphatic group having from 3 to 6 carbon atoms and having two points of attachment, for example, cyclopropylene, cyclobutylene, cyclopentylene, and cyclohexylene.
  • As used herein, “halo” or “halogen” refers to F, Cl, Br, or I.
  • As used herein “heterocycloC3-6alkyl” or “heterocycloalkyl” refers to an aliphatic cyclic moiety that includes from 3-6 carbon atoms, in addition to 1, 2 or 3 heteroatoms that are N, O, or S.
  • As used herein, “stereoisomers” refers to all enantiomerically/diastereomerically pure and enantiomerically/diastereomerically enriched compounds of the invention. Atropisomers, that is, stereoisomers resulting from hindered rotation about single bonds, are also within the scope of the term, “stereoisomers.”
  • As used herein, “pharmaceutically acceptable salt” refers to a salt of a compound of the invention that is generally considered safe for pharmaceutical use. Examples include, for example, hydrochloric acid, sulfuric, fumaric, succinic, ascorbic, maleic, methanesulfonic, and isoethonic acid salts.
  • Compounds for use within the scope of the invention can be prepared according to methods known in the art. For example, certain phenylpyrimidine compounds within the scope of formula I can be prepared according to the sequence set forth in Scheme 1. Those skilled in the art can readily access the enantiomers using a comparable sequence of reactions.
  • Figure US20170173016A1-20170622-C00025
  • Phenylpyrimidine compounds within the scope of formula I that can be made according to the procedures set forth in Scheme 1 include, for example, those of Table 3.
  • TABLE 3
    Figure US20170173016A1-20170622-C00026
    CNDR# X R Y
    51549 N CH3 (S) F
    N CH3 (R) F
    N CH3 (S,R) F
    51550 N H F
    51552 CH CH3 (S) F
    CH CH3 (R) F
    CH CH3 (S,R) F
    51553 CH H F
    51554 N CH3 (S)
    Figure US20170173016A1-20170622-C00027
    N CH3 (R)
    Figure US20170173016A1-20170622-C00028
    N CH3 (S,R)
    Figure US20170173016A1-20170622-C00029
    51557 CH H
    Figure US20170173016A1-20170622-C00030
    51560 CH H OtBu
    51561 CH CH3 (S)
    Figure US20170173016A1-20170622-C00031
    51562 CH CH3 (S)
    Figure US20170173016A1-20170622-C00032
  • Certain triazolopyrimidine compounds within the scope of formula II can be prepared according to the sequence set forth in Scheme 2. Those skilled in the art can readily access the enantiomers using a comparable sequence of reactions.
  • Figure US20170173016A1-20170622-C00033
  • Triazolopyrimidine compounds of formula II that can be prepared according to the procedures set forth in Scheme 2 include, for example, those set forth in Table 4.
  • TABLE 4
    Figure US20170173016A1-20170622-C00034
    CNDR# R Y
    51539 (7) H F
    51551 CH3 (S) F
    CH3 (R) F
    CH3 (S,R) F
    51533 Cevipabulin (8) CH3 (S)
    Figure US20170173016A1-20170622-C00035
    CH3 (R)
    Figure US20170173016A1-20170622-C00036
    CH3 (S,R)
    Figure US20170173016A1-20170622-C00037
    51534 (9) H
    Figure US20170173016A1-20170622-C00038
    51555 CH3 (S)
    Figure US20170173016A1-20170622-C00039
    CH3 (R)
    Figure US20170173016A1-20170622-C00040
    CH3 (S,R)
    Figure US20170173016A1-20170622-C00041
    51556 CH3 (S)
    Figure US20170173016A1-20170622-C00042
    CH3 (R)
    Figure US20170173016A1-20170622-C00043
    CH3 (S,R)
    Figure US20170173016A1-20170622-C00044
    51569 CH3 (S)
    Figure US20170173016A1-20170622-C00045
    51567 CH3 (S)
    Figure US20170173016A1-20170622-C00046
    51570 CH3 (S)
    Figure US20170173016A1-20170622-C00047
    51572 CH3 (S)
    Figure US20170173016A1-20170622-C00048
    51588 CH3 (S)
    Figure US20170173016A1-20170622-C00049
    51591 CH3 (S)
    Figure US20170173016A1-20170622-C00050
    51589 CH3 (S)
    Figure US20170173016A1-20170622-C00051
    51593 CH3 (S)
    Figure US20170173016A1-20170622-C00052
    51595 CH3 (S)
    Figure US20170173016A1-20170622-C00053
    51596 CH3 (S)
    Figure US20170173016A1-20170622-C00054
    51598 CH3 (S)
    Figure US20170173016A1-20170622-C00055
    51599 CH3 (S)
    Figure US20170173016A1-20170622-C00056
  • Compounds of formula III can be prepared, for example, according to the sequence depicted in Scheme 3.
  • Figure US20170173016A1-20170622-C00057
  • Certain preferred compounds of formula IV can be prepared according to the sequences depicted in Schemes 4A and 4B.
  • Figure US20170173016A1-20170622-C00058
    Figure US20170173016A1-20170622-C00059
  • Figure US20170173016A1-20170622-C00060
  • The MT-stabilizing properties of triazolopyrimidines was investigated in a cell-free MT-polymerization assay, as well in a cell-based assay (HEK/QBI 293 cells) that measures changes in acetyl-tubulin (AcTub), a biomarker of stable MTs. (Laferriere, N.; MacRae, T.; Brown, D. Tubulin synthesis and assembly in differentiating neurons. Biochemistry and Cell Biology 1997, 75, 103-117; Black, M.; Baas, P.; Humphries, S. Dynamics of alpha-tubulin deacetylation in intact neurons. J Neurosci 1989, 9, 358). The results from the cell-free studies (data not shown) are in complete agreement with a published report (Beyer, C. F.; Zhang, N.; Hernandez, R.; Vitale, D.; Lucas, J.; Nguyen, T.; Discafani, C.; Ayral-Kaloustian, S.; Gibbons, J. J. TTI-237: a novel microtubule-active compound with in vivo antitumor activity. Cancer Res 2008, 68, 2292-300) and confirmed that the triazolopyri-midines exhibit MT-stabilizing activity similar to that of paclitaxel. The results of the cell-based studies, summarized in FIG. 1, revealed that triazolopyrimidines 7, 8, and 9 (see Table 4) produce a dose-dependent elevation in AcTub. Furthermore, these compounds caused significant increases of detyrosinated α-tubulin (GluTub), another marker of stable MTs (data not shown). Notably, both 8 and 9 were found to be significantly more effective than epoD at 100 nM (FIG. 1).
  • To confirm these results and to ensure that triazolopyrimidine treatment results in an increased organization of the MT-network, rather than disorganized tubulin aggregates, MT structure in HEK/QBI293 cells as determined by AcTub immunofluo-rescence was examined after 4 h of incubation with cevipabulin. Cells that were treated with 100 nM cevipabulin (8) revealed a large increase in highly organized, AcTub-positive MTs relative to control cells, with the intensity of staining exceeding that observed with 100 nM of the known MT-stabilizing agent, epothilone D (epoD). In contrast, the MT-destabilizing agent, colchicine, led to a significant loss of AcTub staining (data not shown).
  • TABLE 5
    Activity of some triazolopyrimidine embodiments of the invention in a cell-based
    assay in which MT stabilization was determined by measuring the relative increase of acetyl-
    tubulin (AcTub) levels after compound treatment.
    Fold-Increase in
    AcTub (dose of
    Structure Compound # maximal effect)
    Figure US20170173016A1-20170622-C00061
         		51588 3.2 (10 μM)
    Figure US20170173016A1-20170622-C00062
         		51589 10.2 (1 μM)
    Figure US20170173016A1-20170622-C00063
         		51593 1.9 (10 μM)
    Figure US20170173016A1-20170622-C00064
         		51591 3.7 (10 μM)
    Figure US20170173016A1-20170622-C00065
         		51555 21.5 (1 μM)
    Figure US20170173016A1-20170622-C00066
         		51556 10.2 (1 μM)
    Figure US20170173016A1-20170622-C00067
         		51533 4.7 (0.1 μM)
    Figure US20170173016A1-20170622-C00068
         		51567 10.1 (1 μM)
    Figure US20170173016A1-20170622-C00069
         		51534 7.2 (1 μM)
  • TABLE 6
    Activity of some phenylpyrimidine and pyridazine embodiments of the invention in a
    cell-based assay in which MT stabilization was determined by measuring the relative increase of
    acetyl-tubulin (AcTub) levels after compound treatment.
    Fold-Increase in
    AcTub (dose of
    Structure Compound # maximal effect)
    Figure US20170173016A1-20170622-C00070
         		51565 4.6 (10 μM)
    Figure US20170173016A1-20170622-C00071
         		51566 2.5 (10 μM)
    Figure US20170173016A1-20170622-C00072
         		51554 4.9 (0.1 μM)
    Figure US20170173016A1-20170622-C00073
         		51557 3.2 (0.1 μM)
    Figure US20170173016A1-20170622-C00074
         		51561 6.1 (0.1 μM)
    Figure US20170173016A1-20170622-C00075
         		51562 6.2 (0.1 μM)
    Figure US20170173016A1-20170622-C00076
         		51549 3.0 (1 μM)
    Figure US20170173016A1-20170622-C00077
         		51552 3.7 (1 μM)
  • TABLE 7
    Brain and plasma levels of some triazolopyrimidine and
    phenylpyrimidine embodiments of the invention 1 hour after
    a 5 mg/kg intraperitoneal injection of compound.
    Compound Brain nM (SD) Plasma nM (SD) Brain/Plasma
    51549 2870 (112) 4946 (151) 0.58
    51552 1479 (112) 4323 (862) 0.34
    51555 1349 (208) 4934 (545) 0.27
    51561 701 (41) 2120 (160) 0.33
  • The MT-stabilizing properties of additional triazolopyrimidines, phenylpyrimidines, and pyridazines was investigated in a cell-free MT-polymerization assay, as well in the aforementioned cell-based assay (HEK/QBI 293 cells) that measures changes in acetyl-tubulin (AcTub), a biomarker of stable MTs (Laferriere, N.; MacRae, T.; Brown, D. Tubulin synthesis and assembly in differentiating neurons. Biochemistry and Cell Biology 1997, 75, 103-117; Black, M.; Baas, P.; Humphries, S. Dynamics of alpha-tubulin deacetylation in intact neurons. J Neurosci 1989, 9, 358). The testing of triazolopyrimidines (Table 5) and phenylpyrimidines (Table 6) in the cell-based studies revealed that a number of examples from each series produce an increase of AcTub relative to vehicle-treated cells, with the magnitude of the increase and the concentration of maximal effect varying among the various examples.
  • For utility in neurodegenerative diseases, MT-stabilizing compounds must cross the blood-brain barrier (BBB) and enter the brain. As summarized in Table 7, a number of examples show concentrations in the brain that exceed 0.5 μM an hour after administration of a 5 mg/kg dose, with brain-to-plasma concentration ratios of ˜0.3 or higher. The relative brain exposures predicted by the one hour analysis of brain and plasma compound levels were confirmed by more complete pharmacokinetic analyses, as exemplified by the profiles of CNDR-51549 and CNDR-51555 shown in FIG. 13. Thus, unlike many previously described MT-stabilizing agents, including cevepabulin, which do not cross the BBB, multiple phenylpyrimidine and triazolopyrimidine examples were unexpectedly found to be brain-penetrant. Moreover, CNDR-51549 was found to cause an increase of AcTub levels in the brains of wild-type mice 3 days after receiving a once-daily 1 mg/kg dose, as shown in FIG. 14. This is reminiscent of what has been demonstrated for other brain-penetrant MT-stabilizing agents (see Brunden K R, Yao Y, Potuzak J S, Ibarz Ferrer N, Ballatore C, James M J, Hogan A L, Trojanowski J Q, Amos Smith A B, III and Lee V M-Y. The Characterization of Microtubule-Stabilizing Drugs as Possible Therapeutic Agents for Alzheimer's Disease and Related Tauopathies. Pharmacol. Res., 2011, 63:341-351), indicating that this and other examples described herein are appropriate for the treatment of neurodegenerative disease.
  • The compounds of formula I can be administered by a variety of methods known to one skilled in the art. Methods of administration include, but are not limited to, intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral routes. The compounds may be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and may be administered together with other biologically active agents. Administration can be systemic or local. In addition, it may be desirable to introduce the compounds into the central nervous system by any suitable route, including intraventricular and intrathecal injection.
  • The practice of the invention can be further understood by reference to the following examples, which are provided by way of illustration and are not intended to be limiting of the invention.
  • Materials and Methods.
  • All solvents were reagent grade. All reagents were purchased from Aldrich or Acros and used as received. Thin layer chromatography (TLC) was performed with 0.25 mm E. Merck pre-coated silica gel plates. Flash chromatography was performed with silica gel 60 (particle size 0.040-0.062 mm) supplied by Silicycle and Sorbent Technologies. Spots were detected by viewing under a UV light. Yields refer to chromatographically and spectroscopically pure compounds. Infrared spectra were recorded on a Jasco Model FT/IR-480 Plus spectrometer. Proton (1H) and carbon (13C) NMR spectra were recorded on a Bruker AMX-500 spectrometer. Chemical shifts were reported relative to solvents. High-resolution mass spectra were measured at the University of Pennsylvania Mass Spectrometry Service on a Waters LCT Premier XE LC/MS system. Analytical reversed-phased (Sunfire™ C18; 4.6×50 mm, 5 mL) high-performance liquid chromatography (HPLC) was performed with a Water binary gradient module 2525 equipped with Waters 2996 PDA and Water micromass ZQ. All samples were analyzed employing a linear gradient from 10% to 90% of acetonitrile in water over 8 minutes and flow rate of 1 mL/min. Preparative reverse phase HPLC purification was performed on a Gilson HPLC system equipped with Gilson 333 pumps, a 215 Liquid Handler, 845Z injection module, and UV detector, employing Waters SunFire™ prep C18 OBD™ columns (5 m 19×50 or 19×100 mm). All samples were purified employing a linear gradient from 10% to 90% of acetonitrile in water over 15 minutes and flow rate of 20 mL/min. Unless otherwise stated, all final compounds were found to be >95% as determined by HPLC/MS and NMR.
  • Figure US20170173016A1-20170622-C00078
    • 5,7-Dichloro-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine
  • Following a reported procedure, (Zhang et al., J. Med. Chem., 2007, 50, 319-327) a slurry of 2-(2,4,6-trifluorophenyl)malonate (1.19 g, 4.10 mmol) and aminotriazole (362 mg, 4.31 mmol) in tributylamine (1.03 μL) was heated to 170° C. for 2 h. The resulting homogeneous brown mixture was cooled to 130° C. and toluene (4 mL) was added before cooling to 50° C. A solution of NaOH (360 μL, 50% aqueous) was added and the precipitated solids were collected by vacuum filtration, washed with cold toluene, and dried to afford the bis-sodium salt of 6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine-5,7-diol as a beige powder (1.24 g, 3.80 mmol, 93% yield).
  • A mixture of bis-sodium 6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine-5,7-diolate (300 mg, 0.9 mmol) and phosphorus oxychloride (1.5 mL, 16 mmol) was heated to 130° C. for 6 h. The reaction mixture was cooled to room temperature and was carefully quenched with H2O (2 mL). This aqueous mixture was extracted with EtOAc (3×5 mL) and the combined organic layers were dried (MgSO4), filtered, and concentrated to an orange oil that was used without further purification (143 mg, 0.448 mmol, 50% yield): 1H NMR (500 MHz, CDCl3) δ 8.62 (s, 1H), 6.94-6.89 (m, 2H); MS (ESI+) 319.00 [M+H+].
    • General Procedure A:
  • According to a reported procedure, (Zhang et al., J. Med. Chem., 2007, 50, 319-327) to 5,7-dichloro-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine (1.0 equiv) in DMF (0.1 M) at room temperature was added i-Pr2NEt (3.0 equiv) and the appropriate amine (3.0 equiv). The orange solution was stirred for 1-6 h and diluted with H2O. The aqueous phase was extracted with 3×10 mL EtOAc, and the combined organic layers were dried (MgSO4), filtered, and concentrated. The acid-sensitive products were purified by reverse-phase HPLC.
  • Figure US20170173016A1-20170622-C00079
    • 5-Chloro-N-(2,2,2-trifluoroethyl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazlo[1,5-a]pyrimidin-7-amine
  • Following General Procedure A using 2,2,2-trifluoroethylamine hydrochloride, reverse-phase HPLC purification afforded the title compound as a colorless solid (14.0 mg, 0.036 mmol, 41% yield): 1H NMR (500 MHz, CDCl3) δ 8.41 (s, 1H), 6.94-6.89 (m, 2H), 6.20 (bs, 1H), 4.20 (dq, J=7.7, 8.1 Hz, 2H). HRMS (ESI+) calculated for C13H7N5F6Cl [M+H+] 382.0294. found 382.0299.
  • Figure US20170173016A1-20170622-C00080
    • (S)-5-Chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
  • Following General Procedure A using (2S)-1,1,1-trifluoro-2-propylamine, reverse-phase HPLC purification afforded the title compound as a colorless solid (42.0 mg, 0.106 mmol, 25% yield): 1H NMR (500 MHz, CDCl3) δ 8.41 (s, 1H), 6.95-6.89 (m, 2H), 5.88 (d, J=9.2 Hz, 1H), 4.69 (bn, 1H), 1.43 (d, J=6.8 Hz, 3H) ppm; MS (ESI+) 396.04 [M+H+].
    • General Procedure B:
  • According to a reported procedure, (Zhang et al., J. Med. Chem., 2007, 50, 319-327; Zhang et al., Bioorg. Med. Chem., 2009, 111-118) to a suspension of NaH (4.0 equiv) in a 2:1 mixture of DMSO and THF (0.35 M) was added the aminoalcohol (4.0 equiv), and the mixture was heated to 60° C. for 1 h. The resulting yellow turbid solution was treated with a solution of trifluoroarene (1.0 equiv) in a 1:1 mixture DMSO and THF (0.5 M). The reaction mixture was stirred at 60° C. for 3 h and monitored by LCMS. If the starting material remained after 3 h, additional NaH (4.0 equiv) and aminoalcohol (4.0 equiv) were added, sequentially, and the reaction mixture was heated for 12 h. Following complete consumption of the starting material, the reaction mixture was cooled to room temperature and diluted with H2O and EtOAc. The organic layer was washed with H2O and brine, and the combined aqueous layers were extracted with EtOAc (×3). The combined organic layers were dried (MgSO4), filtered, and concentrated. The crude products were purified by reverse-phase HPLC.
  • Figure US20170173016A1-20170622-C00081
    • 5-Chloro-6-(2,6-difluoro-4-(3-(methylamino)propoxy)phenyl)-N-(2,2,2-trifluoroethyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
  • Following General Procedure B using 3-(methylamino)-1-propanol and 5-chloro-N-(2,2,2-trifluoroethyl)-6-(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound as a colorless solid (6.1 mg, 0.014 mmol, 13% yield): MS (ESI+) 450.69 [M+H+].
  • Figure US20170173016A1-20170622-C00082
    • (S)-5-Chloro-6-(2,6-difluoro-4-(3-(methylamino)propoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
  • Following General Procedure B using 3-(methylamino)-1-propanol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification of the crude product (105 mg) afforded the title compound as a colorless solid (43.1 mg, 0.093 mmol, 35% yield): 1H NMR (500 MHz, DMSO-d6) δ 8.29 (s, 2H), 6.81 (dd, J=2.8, 9.4 Hz, 2H), 5.84-5.78 (m, 1H), 4.14 (t, J=5.4 Hz, 2H), 3.02 (t, J=6.8 Hz, 2H), 2.56 (bs, 3H), 2.06 (bm, 2H), 1.28 (d, J=6.7 Hz, 3H) ppm; HRMS (ESI+) calculated for C18H19N6OF5Cl [M+H+] 465.1229. found 465.1230.
  • Figure US20170173016A1-20170622-C00083
    • (S)-5-Chloro-6-(4-(3-(dimethylamino)propoxy)-2,6-difluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
  • Following General Procedure B using 3-dimethylamino-1-propanol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound as a colorless, hygroscopic solid (9.2 mg, 0.019 mmol, 38% yield): 1H NMR (500 MHz, DMSO-d6) δ 8.51 (bs, 1H), 8.18 (s, 1H), 6.89 (dd, J=4.0, 9.9 Hz, 2H), 5.89-5.83 (m, 1H), 4.10 (t, J=6.3 Hz, 2H), 2.55 (t, J=7.6 Hz, 2H), 2.29 (s, 6H), 1.93 (p, J=6.8 Hz, 2H), 1.37 (d, J=6.8 Hz, 3H) ppm; HRMS (ESI+) calculated for C19H21N6OF5Cl [M+H+] 479.1386. found 479.1384.
  • Figure US20170173016A1-20170622-C00084
    • (S)-5-Chloro-6-(2,6-difluoro-4-(3-(methylamino)cyclobutoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
  • Following General Procedure B using 3-(methylamino)-1-cyclobutanol (2.5:1 cis/trans isomers) and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound as a light yellow, hygroscopic solid (8.9 mg, 0.019 mmol, 33% yield) as a 2.5:1 mixture of cis/trans isomers: 1H NMR (500 MHz, DMSO-d6) major isomer δ 8.35 (bs, 1H), 8.23 (s, 1H), 6.74 (dd, J=4.2, 9.7 Hz, 2H), 5.85-5.79 (m, 1H), 4.59 (pent, J=7.0 Hz, 1H), 3.16 (pent, J=7.7 Hz, 1H), 2.89-2.84 (m, 2H), 2.39 (s, 3H), 2.11-2.06 (m, 2H), 1.30 (d, J=6.7 Hz, 3H); minor isomer (distinctive signals) δ 6.69-6.71 (m, 2H), 4.96-4.93 (m, 1H), 3.62-3.59 (m, 1H), 2.40 (s, 3H); HRMS (ESI+) calculated for C19H19N6OF5Cl [M+H+] 477.1229. found 477.1221.
  • Figure US20170173016A1-20170622-C00085
    • 4,6-Dichloro-2-(pyrazin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine
  • A mixture of diethyl 2-(2,4,6-trifluorophenyl)malonate (250 mg, 0.861 mmol), 2-pyrazinecarboxamidine hydrochloride (144 mg, 0.904 mmol, 1.05 equiv), and tributylamine (221 μL [172 mg], 1.08 equiv) was stirred under nitrogen atmosphere at 180° C. for 1 h in a sealed tube. The mixture was cooled to room temperature and treated with 1.0 N hydrochloric acid. The precipitates were collected by filtration, washed with water and dried to give 2-pyrazin-2-yl-5-(2,4,6-trifluorophenyl)pyrimidine-4,6-diol as a dark tan solid (163 mg), which was used directly in the next step.
  • A mixture of 2-pyrazin-2-yl-5-(2,4,6-trifluorophenyl)pyrimidine-4,6-diol (163 mg) in phosphorous oxychloride (2.03 mL, 21.9 mmol, 43 equiv) and 2,6-lutidine (404 μL, 3.51 mmol, 6.9 equiv) was heated at 110° C. for 16 h in a sealed tube. The excess phosphorous oxychloride was removed in vacuo, and the resulting residue was dissolved in ethyl acetate. The organic layer was washed with water and saturated sodium chloride, dried over sodium sulfate, and concentrated. The residue was purified by silica gel chromatography over silica gel, eluting with a gradient of 20% ethyl acetate in hexanes to 33% ethyl acetate in hexanes. Concentration provided 104 mg of the title compound as a light yellow solid (32% over two steps). 1H-NMR (500 MHz; CDCl3): δ 9.73 (s, 1H), 8.84 (s, 1H), 8.77 (s, 1H), 6.88-6.84 (m, 2H) ppm.
  • Figure US20170173016A1-20170622-C00086
    • 4,6-Dichloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine
  • Prepared as 4,6-Dichloro-2-(pyrazin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine from picolinimidamide hydrochloride and 2-(2,4,6-trifluorophenyl)malonate. Yield: 58% over two steps.
  • 1H-NMR (500 MHz; CDCl3): δ 9.16 (d, J=5.4 Hz, 1H), 9.00-8.98 (m, 1H), 8.78 (td, J=7.9, 1.2 Hz, 1H), 8.36 (t, J=6.7 Hz, 1H), 6.88 (dd, J=8.4, 7.5 Hz, 2H) ppm.
  • Figure US20170173016A1-20170622-C00087
    • (S)-6-chloro-2-(pyrazin-2-yl)-5-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51549)
  • A mixture of 4,6-Dichloro-2-(pyrazin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine (71 mg, 0.199 mmol), (S)-2,2,2-trifluoro-1-methylethylamine (68 μL, [78 mg] 0.696 mmol, 3.5 equiv), and in N,N-dimethylformamide (1.73 mL, 22.5 mmol) was stirred at 90° C. in a sealed tube for 18 h. The reaction mixture was partitioned between ethyl acetate and saturated sodium chloride. The organic layer was washed with saturated sodium chloride (3×), dried over sodium sulfate, and concentrated. The residue was purified by silica gel chromatography, using gradients of ethyl acetate in hexanes. Concentration provided the desired compound as a white solid. Yield: 18% 1H-NMR (500 MHz; DMSO-d6): δ 9.57 (d, J=1.4 Hz, 1H), 8.85-8.83 (m, 2H), 7.70 (d, J=8.8 Hz, 1H), 7.48-7.42 (m, 2H), 5.52 (tt, J=13.6, 6.7 Hz, 1H), 1.35 (d, J=7.1 Hz, 3H) ppm. HRMS ESI+: calculated for C17H11ClF6N5 434.0607. found 434.0616.
  • Figure US20170173016A1-20170622-C00088
    • 6-Chloro-2-(pyrazin-2-yl)-N-(2,2,2-trifluoroethyl)-5-(2,4,6-trifluorophenyl)pyrimidin-4-amine (CNDR-51550)
  • Prepared as CNDR-51549 from 4,6-Dichloro-2-(pyrazin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine and 2,2,2-trifluoroethylamine. Yield: 31%. 1H-NMR (500 MHz; CDCl3): δ 9.65 (d, J=1.4 Hz, 1H), 8.79 (dd, J=2.4, 1.5 Hz, 1H), 8.72 (d, J=2.4 Hz, 1H), 6.89-6.85 (m, 2H), 5.21-5.18 (m, 1H), 4.37 (qd, J=8.7, 6.6 Hz, 2H) ppm. HRMS [ESI]+: calculated for C1-6H9ClF6N5 420.0451. found: 420.0459.
  • Figure US20170173016A1-20170622-C00089
    • (S)-6-chloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51552)
  • Prepared as CNDR-51549 from 4,6-Dichloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine and (S)-2,2,2-trifluoro-1-methylethylamine.
  • 1H-NMR (500 MHz; CDCl3): δ 8.86 (d, J=4.6 Hz, 1H), 8.43 (d, J=7.9 Hz, 1H), 7.90-7.87 (m, 1H), 7.44 (dd, J=7.2, 5.0 Hz, 1H), 6.92-6.86 (m, 2H), 5.41-5.35 (m, 1H), 4.60 (d, J=9.3 Hz, 1H), 1.41 (d, J=7.0 Hz, 3H) ppm.
  • HRMS [ESI]−: calculated for C18H10ClF6N4 431.0498. found: 431.0508.
  • Figure US20170173016A1-20170622-C00090
    • 6-Chloro-2-(pyridin-2-yl)-N-(2,2,2-trifluoroethyl)-5-(2,4,6-trifluorophenyl)pyrimidin-4-amine (CNDR-51553)
  • Prepared as CNDR-51549 from 4,6-Dichloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)pyrimidine and (S)-2,2,2-trifluoroethylamine. Yield 12%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.83 (d, J=4.0 Hz, 1H), 8.43 (d, J=7.9 Hz, 1H), 7.88 (t, J=7.3 Hz, 1H), 7.44 (t, J=5.8 Hz, 1H), 6.84-6.81 (m, 2H), 5.04 (t, J=6.0 Hz, 1H), 4.38 (dd, J=15.4, 8.0 Hz, 2H) ppm.
  • HRMS [ESI]+: calculated for C17H10ClF6N4 419.0498. found: 419.0496.
  • Figure US20170173016A1-20170622-C00091
    • (S)-6-Chloro-5-(4-(3-(dimethylamino)propoxy)-2,6-difluorophenyl)-2-(pyrazin-2-yl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51554)
  • To a solution of CNDR-51549 (27 mg, 0.062 mmol) and 3-(dimethylamino)propan-1-ol (38 μL, 0.321 mmol) in dimethylsulfoxide (322 mL) was added sodium hydride (60% in mineral oil, 13 mg, 0.321 mmol) at room temperature. The reaction mixture was stirred at 60° C. for 2 h, cooled to room temperature, dissolved in additional DMSO, filtered, and purified by preparative reverse phase HPLC. Concentration provided the title compound as a white solid. Yield: 8%.
  • 1H-NMR (500 MHz; DMSO-d6): δ 9.58 (d, J=1.2 Hz, 1H), 8.86-8.84 (m, 2H), 7.70 (d, J=8.8 Hz, 1H), 6.95 (t, J=10.0 Hz, 2H), 5.53 (dd, J=15.3, 7.6 Hz, 1H), 4.12 (t, J=6.2 Hz, 2H), 2.38 (t, J=7.1 Hz, 2H), 2.17 (s, 6H), 1.90 (quintet, J=6.7 Hz, 2H), 1.36 (d, J=7.1 Hz, 3H) ppm.
  • HRMS [ESI]+: calculated for C22H23ClF5N6O 517.1542. found: 517.1536.
  • Figure US20170173016A1-20170622-C00092
    • 6-Chloro-5-(4-(3-(dimethylamino)propoxy)-2,6-difluorophenyl)-2-(pyridin-2-yl)-N-(2,2,2-trifluoroethyl)pyrimidin-4-amine (CNDR-51557)
  • Prepared as CNDR-51554 from (S)-6-chloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51552) and 3-(dimethylamino)propan-1-ol.
  • 1H-NMR (500 MHz; MeOD): δ 8.72 (dd, J=4.7, 0.7 Hz, 1H), 8.54-8.52 (m, 1H), 8.03 (td, J=7.8, 1.7 Hz, 1H), 7.58 (ddd, J=7.5, 4.9, 1.0 Hz, 1H), 6.79 (d, J=9.3 Hz, 2H), 4.38 (q, J=9.1 Hz, 2H), 4.14 (t, J=6.0 Hz, 2H), 2.73 (t, J=7.6 Hz, 2H), 2.45 (s, 6H), 2.07 (dd, J=13.9, 7.3 Hz, 2H) ppm.
  • Figure US20170173016A1-20170622-C00093
    • 5-(4-(tert-butoxy)-2,6-difluorophenyl)-6-chloro-2-(pyridin-2-yl)-N-(2,2,2-trifluoroethyl)pyrimidin-4-amine (CNDR-51560)
  • To a solution of 6-Chloro-2-(pyridin-2-yl)-N-(2,2,2-trifluoroethyl)-5-(2,4,6-trifluorophenyl)-pyrimidin-4-amine (14 mg, 0.0334 mmol) in THF (198 μl), potassium tert-butoxide (1M THF solution, 66.9 μl) was added at room temperature. The reaction mixture was stirred for 1 h at room temperature and then partitioned between water and DCM. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. Purification by silica gel preparative TLC using 20% ethyl acetate in hexanes as eluent, furnished the desired product.
  • 1H-NMR (500 MHz; CDCl3): δ 8.91 (s, 1H), 8.51-8.50 (m, 1H), 7.95-7.94 (m, 1H), 7.50-7.48 (m, 1H), 6.72 (d, J=9.1 Hz, 2H), 4.99 (s, 1H), 4.45 (dt, J=2.0, 1.3 Hz, 2H), 1.49 (s, 9H) ppm.
  • HRMS [ESI]+: calculated for C21H19ClF5N4O 473.1168. found: 473.1156.
  • Figure US20170173016A1-20170622-C00094
    • 4-Chloro-N-methoxy-N-methylbenzamide
  • Commercially available 4-chlorobenzoic acid (3.4913 g, 22.3 mmol, 1.00 equiv) was suspended in CH2Cl2 (30 mL) and cooled to 0° C. at which time Me(OMe)NH.HCl (2.39 g, 24.5 mmol, 1.10 equiv), N-methymorpholine (2.48 g, 2.70 mL, 24.5 mmol, 1.10 equiv), and N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (4.70 g, 24.5 mmol, 1.10 equiv) were added sequentially. After stirring for 12 h the reaction was quenched with NH4Cl (sat. aq.) and the layers were separated. The aqueous layer was back extracted with CH2Cl2 (3×). The combined organic layers were washed with H2O, brine, dried over Na2SO4, filtered and concentrated. The crude residue was purified via Silica gel flash chromatography (1:1 EtOAc/Hex) to give 3.929 g (88%) of the title compound as a clear oil. The spectral data was identical to that reported in the literatureIV: 1H NMR (500 MHz, CDCl3) δ 7.68-7.54 (m, 2H), 7.40-7.29 (m, 2H), 3.49 (s, 3H), 3.31 (s, 3H) ppm.
  • Figure US20170173016A1-20170622-C00095
    • 1-(4-chlorophenyl)Propan-1-one
  • 4-Chloro-N-methoxy-N-methylbenzamide (0.5352 g, 2.68 mmol, 1.00 equiv) was dissolved in Et2O (10 mL) and cooled to 0° C. Ethylmagnesium bromide (1.80 mL, 5.36 mmol, 2.00 equiv, 3M solution in Et2O) was added dropwise. After stirring for 3 h the reaction was quenched with NH4Cl (sat. aq.) and the layers were separated. The aqueous layer was back extracted with Et2O (3×). The combined organic layers were washed with H2O, brine, dried over Na2SO4, filtered and concentrated. Purification by silica gel column chromatography using a 1:1 mixture of ethyl acetate in hexanes as eluant furnished the title compound (0.349 g) as a clear oil. Yield: 77%. The spectral data was identical to that reported in the literatureV: 1H NMR (500 MHz, CDCl3): δ 7.94-7.89 (m, 2H), 7.49-7.38 (m, 2H), 2.97 (q, J=7.2 Hz, 2H), 1.22 (t, J=7.2 Hz, 3H) ppm.
  • Figure US20170173016A1-20170622-C00096
    • 2-Bromo-1-(4-chlorophenyl)propan-1-one
  • 1-(4-chlorophenyl)Propan-1-one (0.2264 g, 1.34 mmol, 1.00 equiv) was dissolved in acetic acid (4 mL) and 1 drop of HBr (48%) was added. Bromine (0.225 g, 0.08 mL, 1.05 equiv) was added dropwise. After 1 h the reaction was carefully quenched with NaHCO3 (sat. aq.) and extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The crude residue was purified via silica gel flash chromatography (25% EtOAc/Hex) to give 0.2897 g (87%) of the title compound as an orange oil. The spectral data was identical to that reported in the literatureVI: 1H NMR (500 MHz, CDCl3): δ 7.99-7.94 (m, 2H), 7.49-7.40 (m, 2H), 5.25 (q, J=6.6 Hz, 1H), 1.91 (s, 3H) ppm.
  • Figure US20170173016A1-20170622-C00097
    • 4-(4-chlorophenyl)-5-Hydroxy-5-methyl-3-(2,4,6-trifluorophenyl)furan-2(5H)-one
  • 2-Bromo-1-(4-chlorophenyl)propan-1-one (0.1783 g, 0.61 mmol, 1.00 equiv) and 2,4,6-trifluorophenylacetic acid (0.245 g, 1.29 mmol, 1.10 equiv) were dissolved in CH3CN (2 mL). Triethylamine (0.130 g, 0.18 mL, 1.29 mmol, 1.10 equiv) was added dropwise and allowed to stir for 12 h. DBU (0.445 g, 0.44 mL, 2.93 mmol, 2.50 equiv) was added dropwise and the resulting dark mixture was allowed to stir for 1 h. Air was then bubbled through the mixture for 5 h. The reaction was quenched with NH4Cl (sat. aq.) and extracted with ethyl acetate (3×). The combined organic extracts were washed with NaHCO3 (sat. aq.), brine, dried over Na2SO4, filtered and concentrated. The crude residue was purified via silica gel flash chromatography (20% EtOAc/Hex) to give 0.199 g (48%) of the title compound as a clear oil: 1H NMR (500 MHz, CDCl3) δ 7.50-7.45 (m, 2H), 7.34-7.27 (m, 2H), 6.80 (tt, J=9.0, 2.1 Hz, 1H), 6.58 (tt, J=9.0, 2.1 Hz, 1H), 5.24 (s, 1H), 1.73 (s, 3H) ppm.
  • Figure US20170173016A1-20170622-C00098
    • 5-(4-chlorophenyl)-6-Methyl-4-(2,4,6-trifluorophenyl)pyridazin-3(2H)-one
  • 4-(4-chlorophenyl)-5-Hydroxy-5-methyl-3-(2,4,6-trifluorophenyl)furan-2(5H)-one (0.141 g, 0.4 mmol, 1.00 equiv) was dissolved in 1-butanol (2.5 mL). Hydrazine hydrate (0.04 g, 0.03 mL, 0.68 mmol, 1.70 equiv) was added dropwise and heated to 120° C. for 24 h. Upon cooling the reaction mixture was placed in the refrigerator overnight. The precipitated solid was collected and washed with hexanes to give the title compound as a white solid: 1H NMR (500 MHz, CDCl3) δ 11.40 (bs, 1H), 7.34-7.28 (m, 2H), 7.07-7.00 (m, 2H), 6.57 (dd, J=8.7, 7.2 Hz, 2H), 2.11 (s, 3H) ppm; 13C NMR (126 MHz, CDCl3) δ 159.86, 147.46, 144.87, 135.21, 133.26, 129.08, 129.00, 100.69 (d, J=25.2 Hz), 20.91 ppm.
  • Figure US20170173016A1-20170622-C00099
    • 3-chloro-5-(4-chlorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine
  • 5-(4-chlorophenyl)-6-Methyl-4-(2,4,6-trifluorophenyl)pyridazin-3(2H)-one (0.0295 g, 0.084 mmol, 1.00 equiv) was dissolved in POCl3 (1 mL) and heated 110° C. for 1 h. After cooling, the mixture was concentrated under reduced pressure. The crude material was taken up in EtOAc and washed with H2O, brine, dried over Na2SO4, and concentrated under reduced pressure. The crude residue was purified via silica gel flash chromatography (40% EtOAc/Hex) to give 0.0311 g (64%) of the title compound as a pale yellow oil: 1H NMR (500 MHz, CDCl3) δ 7.36-7.28 (m, 2H), 7.06-6.96 (m, 2H), 6.68-6.56 (m, 2H), 2.53 (s, 3H) ppm; 13C NMR (126 MHz, CDCl3) δ 158.60, 155.55, 142.73, 135.49, 132.70, 129.26, 129.05, 128.15, 100.91 (d, J=26.2 Hz), 21.35 ppm.
  • Figure US20170173016A1-20170622-C00100
    • Methyl 3-(2-(2,4,6-trifluorophenyl)acetamido)pyrazine-2-carboxylate
  • 2,4,6-Trifluorophenylacetic acid (0.4710 g, 2.48 mmol, 1.00 equiv) was dissolved in CH2Cl2 (4 mL) and two drops of DMF was added. Oxalyl chloride (0.377 g, 0.26 mL, 2.97 mmol, 1.20 equiv) was added dropwise and stirred for 30 minutes at room temperature. The solution was heated to reflux and stirred for 2 h. After cooling to room temperature the crude acid chloride was used directly in the next step without purification. The reaction mixture containing the acid chloride in CH2Cl2 (4 mL) was added dropwise to a solution containing methyl 3-aminopyrazine-2-carboxylate (0.3794 g, 2.48 mmol, 1.00 equiv), pyridine (0.372 g, 0.38 mL, 4.71 mmol, 1.90 equiv), and DMAP (catalytic quantities). The reaction mixture was stirred for 20 h and then diluted with CH2Cl2 (100 mL) and washed with water, 1 N HCl, and brine. The organic layers was dried over Na2SO4, concentrated under reduced pressure, and purified via silica gel flash chromatography to deliver 0.2362 g (29%) of the title compound as an orange solid. The spectral data was identical to that reported in the literature. 1H NMR (500 MHz, CDCl3) δ 10.82 (s, 1H), 8.59 (d, J=2.3 Hz, 1H), 8.41 (d, J=2.3 Hz, 1H), 6.73 (dd, J=8.7, 7.3 Hz, 2H), 4.03 (s, 5H) ppm.
  • Figure US20170173016A1-20170622-C00101
    • 8-Hydroxy-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazin-6(5H)-one
  • Methyl 3-(2-(2,4,6-trifluorophenyl)acetamido)pyrazine-2-carboxylate (0.2239 g, 0.69 mmol, 1.00 equiv) and anhydrous K2CO3 (0.1903 g, 1.38 mmol, 2.00 equiv) were suspended in DMF (4 mL) and heated to 80° C. for 3 h. After cooling to room temperature the mixture was poured into ice-cold water, acidified to a pH of 3 with 1 N HCl, and extracted with EtOAc (3×). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give 0.1783 g (88%) of the title compound as a yellow powder. The spectral data was identical to that reported in the literature.VII 1H NMR (500 MHz, DMSO-d6) δ 10.80 (s, 1H), 8.70 (d, J=2.3 Hz, 1H), 8.56 (d, J=2.3 Hz, 1H), 7.22 (m, 2H) ppm.
  • Figure US20170173016A1-20170622-C00102
    • 6,8-Dichloro-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazine
  • 8-Hydroxy-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazin-6(5H)-one (0.1783 g, 0.61 mmol, 1.00 equiv) and DMF (0.089 g, 0.095 mL, 1.22 mmol, 2.00 equiv) were dissolved in DCE (5 mL) and heated to 80° C. POCl3 (0.373 g, 0.23 mL, 2.43 mmol, 4.00 equiv) was added dropwise at this temperature. After the addition, the reaction was stirred for 3 h allowing the temperature to cool to room temperature. 50 mL of NaHCO3 (sat. aq.) was added and the solution was stirred for 30 min. The reaction mixture was then extracted with EtOAc (3×) and the combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The spectral data was identical to that reported in the literature.VII 1H NMR (500 MHz, CDCl3) δ 9.17 (d, J=2.1 Hz, 1H), 9.11 (d, J=2.1 Hz, 1H), 6.86 (dd, J=8.6, 7.6 Hz, 2H) ppm.
  • Figure US20170173016A1-20170622-C00103
    • 6-Chloro-N-isopropyl-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazin-8-amine and 8-chloro-N-isopropyl-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazin-6-amine
  • 6,8-Dichloro-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazine (0.1616 g, 0.49 mmol, 1.00 equiv) and DMAP (0.022 g, 0.09 mmol, 0.19 equiv) were dissolved in DMF (2 mL). Anhydrous potassium carbonate (0.346 g, 2.51 mmol, 1.55 equiv) and isopropylamine (0.148 g, 0.21 mL, 2.51 mmol, 1.55 equiv) were added consecutively and the mixture was allowed to stir for 24 h at room temperature. The reaction was poured into ice water and extracted with EtOAc (3×). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. Purification by silica gel preparative thin layer chromatography using a 1:1 mixture of ethyl acetate in hexanes as eluent furnished the title compound and 8-chloro-N-isopropyl-7-(2,4,6-trifluorophenyl)pyrido[2,3-b]pyrazin-6-amine. The spectral data of both compounds were identical to that reported in the literature.VII C-8 alkylated pyridopyrazine: 1H NMR (500 MHz, CDCl3) δ 8.99 (d, J=1.9 Hz, 1H), 8.66 (d, J=1.8 Hz, 1H), 6.93 (bs, 1H), 6.83 (dd, J=8.6, 7.6 Hz, 2H), 3.36 (m, 1H), 1.11 (d, J=6.3 Hz, 6H) ppm. C-6 alkylated pyridopyrazine: 1H NMR (500 MHz, CDCl3) δ 8.84 (d, J=2.0 Hz, 1H), 8.63 (d, J=2.0 Hz, 1H), 6.93 (dd, J=8.6, 6.9 Hz, 2H), 4.72-4.60 (m, 1H), 4.54 (s, 1H), 1.24 (d, J=6.5 Hz, 6H) ppm.
  • Figure US20170173016A1-20170622-C00104
    • (S)-5-Chloro-6-(2,6-difluoro-4-(3-(pyrrolidin-1-yl)propoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51569)
  • Following General Procedure B using 3-(pyrrolidin-1-yl)propan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound as formic acid salt. Yield: 35%.
  • 1H-NMR (500 MHz; CDCl3): δ 12.42 (s, 1H), 8.36 (s, 1H), 6.60 (d, J=9.1 Hz, 2H), 5.92 (d, J=10.2 Hz, 1H), 4.97 (broad s, 1H), 4.13 (t, J=5.5 Hz, 2H), 3.89 (m, 2H), 3.80-3.78 (m, 2H), 3.34 (m, 2H), 2.86 (m, 2H), 2.33 (m, 2H), 2.16 (m, 2H), 1.39 (d, J=6.8 Hz, 3H) ppm. HRMS (ESI+) calculated for C21H23ClF5N6O [M+H+]: 505.1542. found 505.1524.
  • Figure US20170173016A1-20170622-C00105
    • (S)-3-(4-(5-chloro-7-((1,1,1-trifluoropropan-2-yl)amino)-[1,2,4]Triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy)propan-1-ol (CNDR-51567)
  • Following General Procedure B using propane-1,3-diol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 60%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.40 (s, 1H), 6.70-6.67 (m, 2H), 5.91 (d, J=8.7 Hz, 1H), 4.77 (broad s, 1H), 4.21 (t, J=6.1 Hz, 2H), 3.91 (t, J=5.9 Hz, 2H), 2.18-2.09 (m, 2H), 1.70 (s, 1H), 1.42 (d, J=6.8 Hz, 3H) ppm. HRMS (ESI+) calculated for C17H1-6ClF5N5O2 [M+H+]: 452.0913. found 452.0902.
  • Figure US20170173016A1-20170622-C00106
    • (S)-6-(4-(3-aminopropoxy)-2,6-difluorophenyl)-5-Chloro-N-(1,1,1-trifuopropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51570)
  • Following General Procedure B using 3-aminopropan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound as formic acid salt. Yield: 22%.
  • 1H-NMR (500 MHz; DMSO-d6): δ 8.30 (s, 1H), 8.09 (d, J=0.3 Hz, 1H), 6.76-6.74 (m, 2H), 5.78 (broad s, 1H), 4.13 (t, J=5.9 Hz, 2H), 3.36 (broad s, 2H), 2.98 (t, J=7.2 Hz, 2H), 2.03 (t, J=6.6 Hz, 2H), 1.21 (d, J=6.5 Hz, 3H) ppm. HRMS (ESI+) calculated for C17H17ClF5N6 [M+H+]: 451.1073. found 451.1076.
  • Figure US20170173016A1-20170622-C00107
    • (S)-6-(4-(2-(3-aminooxetan-3-yl)ethoxy)-2,6-Difluorophenyl)-5-chloro-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51572)
  • Following General Procedure B using 2-(1-aminocyclobutyl)ethan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound as trifluoroacetic acid salt. Yield: 44%. HRMS (ESI+) calculated for C19H19ClF5N6O2 [M+H+] 493.1178. found 493.1177.
  • Figure US20170173016A1-20170622-C00108
    • (S)-5-Chloro-6-(2,6-difluoro-4-(3-fluoropropoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51588)
  • Following General Procedure B using 3-chloropropan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 66%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.39 (s, 1H), 6.69-6.65 (m, 2H), 5.89 (d, J=9.2 Hz, 1H), 4.76 (m, 1H), 4.73 (t, J=5.6 Hz, 1H), 4.63 (t, J=5.6 Hz, 1H), 4.18 (t, J=6.1 Hz, 2H), 2.29-2.20 (m, 2H), 1.41 (d, J=6.8 Hz, 3H) ppm. HRMS (ESI+) calculated for C17H15N5OF6Cl [M+H+]: 454.0864. found 454.0858.
  • Figure US20170173016A1-20170622-C00109
    • (S)-5-Chloro-6-(4-(3-chloropropoxy)-2,6-difluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51591)
  • Following General Procedure B using 3-fluoropropan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 86%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.41 (s, 1H), 6.68 (m, 2H), 5.89 (d, J=9.8 Hz, 1H), 4.79 (broad s, 1H), 4.21 (t, J=5.8 Hz, 2H), 3.79 (t, J=6.2 Hz, 2H), 2.32 (m, 2H), 1.43 (d, J=6.8 Hz, 3H) ppm. HRMS (ESI+) calculated for C17H15N5OF5Cl2 [M+H+]: 470.0568. found 470.0578.
  • Figure US20170173016A1-20170622-C00110
    • (S)—N-(3-(4-(5-chloro-7-((1,1,1-trifluoropropan-2-yl)amino)-[1,2,4]Triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy)propyl)acetamide (CNDR-51589)
  • Following General Procedure B using N-(3-hydroxypropyl)acetamide and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 90%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.37 (s, 1H), 6.64 (d, J=8.9 Hz, 2H), 6.11 (s, 1H), 5.98 (d, J=10.6 Hz, 1H), 4.85 (s, 1H), 4.10 (t, J=6.1 Hz, 2H), 3.48 (q, J=6.3 Hz, 2H), 2.08 (t, J=6.4 Hz, 2H), 2.01 (s, 3H), 1.42 (d, J=6.8 Hz, 3H) ppm. HRMS (ESI+) calculated for C19H19ClF5N6O2 [M+H+]: 493.1178. found 493.1180.
  • Figure US20170173016A1-20170622-C00111
    • (S)—N-(3-(4-(5-chloro-7-((1,1,1-trifluoropropan-2-yl)amino)-[1,2,4]Triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy)propyl)-N-methylacetamide (CNDR-51593)
  • Following General Procedure B using N-(3-hydroxypropyl)-N-methylacetamide and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 62%.
  • IR: v 3411, 3207, 2923, 2853, 1638, 1616 cm−1.
  • HRMS (ESI+) calculated for C20H21ClF5N6O2 [M+H+]: 507.1335. found 507.1335.
  • Figure US20170173016A1-20170622-C00112
    • (S)—N-(3-(4-(5-chloro-7-((1,1,1-trifluoropropan-2-yl)amino)-[1,2,4]Triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy)propyl)pivalamide (CNDR-51595)
  • Following General Procedure B using N-(3-hydroxypropyl)pivalamide and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 38%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.39 (s, 1H), 6.64 (m, 2H), 5.96 (m, 2H), 4.77 (broad s, 1H), 4.10 (t, J=5.9 Hz, 2H), 3.49 (q, J=6.3 Hz, 2H), 2.07 (m, 2H), 1.41 (d, J=6.8 Hz, 3H), 1.22 (s, 9H) ppm. HRMS (ESI+) calculated for C22H25N6O2F5Cl [M+H+]: 535.1642. found 535.1641.
  • Figure US20170173016A1-20170622-C00113
    • (S)-5-Chloro-6-(2,6-difluoro-4-(3-morpholinopropoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51596)
  • Following General Procedure B using 3-morpholinopropan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 68%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.39 (s, 1H), 6.67-6.63 (m, 2H), 5.95 (d, J=10.5 Hz, 1H), 4.81 (broad s, 1H), 4.11 (t, J=6.1 Hz, 2H), 3.82 (t, J=4.7 Hz, 4H), 2.75 (m, 6H), 2.13 (m, 2H), 1.41 (d, J=6.8 Hz, 3H) ppm. IR: v 3425, 2958, 2861, 2817, 1640, 1615, 1578 cm−1. HRMS (ESI+) calculated for C21H23N6O2F5Cl [M+H+]: 521.1486. found 521.1488.
  • Figure US20170173016A1-20170622-C00114
    • (S)-5-Chloro-6-(2,6-difluoro-4-(3-(phenylamino)propoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51598)
  • Following General Procedure B using 3-(phenylamino)propan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 53%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.40 (s, 1H), 7.20 (m, 2H), 6.73 (m, 1H), 6.67 (m, 4H), 5.89 (d, J=10.1 Hz, 1H), 4.77 (broad s, 1H), 4.16 (t, J=5.9 Hz, 2H), 3.40 (t, J=6.6 Hz, 2H), 2.17 (quintet, J=6.2 Hz, 2H), 1.41 (d, J=6.8 Hz, 3H) ppm. IR: v 3338, 3209, 3113, 3055, 2950, 1614, 1575 cm−1. HRMS (ESI+) calculated for C23H21N6OF5Cl [M+H+]: 527.1380. found 527.1385.
  • Figure US20170173016A1-20170622-C00115
    • (S)-5-chloro-6-(2,6-difluoro-4-(3-((2,2,2-trifluoroethyl)amino)propoxy)phenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine (CNDR-51599)
  • Following General Procedure B using 3-((2,2,2-trifluoroethyl)amino)propan-1-ol and (S)-5-chloro-6-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, reverse-phase HPLC purification afforded the title compound. Yield: 89%.
  • 1H-NMR (500 MHz; CDCl3): δ 8.40 (s, 1H), 6.69-6.65 (m, 2H), 5.92 (d, J=10.3 Hz, 1H), 4.77 (broad s, 1H), 4.15 (t, J=6.1 Hz, 2H), 3.25 (q, J=9.4 Hz, 2H), 2.99 (t, J=6.7 Hz, 2H), 2.04 (quintet, J=6.4 Hz, 2H), 1.42 (d, J=6.8 Hz, 3H). HRMS (ESI+) calculated for C19H18ClF8N6O [M+H+]: 533.1103. found 533.1199.
  • Figure US20170173016A1-20170622-C00116
    • (S)-6-Chloro-5-(4-(3-(dimethylamino)propoxy)-2,6-difluorophenyl)-2-(pyridin-2-yl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51561)
  • Prepared as CNDR-51554 from (S)-6-chloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51552) and 3-(dimethylamino)propan-1-ol.
  • Yield: 7%.
  • HRMS [ESI]+: calculated for C23H24ClF5N5O: 516.1590. found: 516.1592.
  • Figure US20170173016A1-20170622-C00117
    • (S)-6-Chloro-5-(2,6-difluoro-4-(3-(methylamino)propoxy)phenyl)-2-(pyridin-2-yl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51562)
  • Prepared as CNDR-51554 from (S)-6-chloro-2-(pyridin-2-yl)-5-(2,4,6-trifluorophenyl)-N-(1,1,1-trifluoropropan-2-yl)pyrimidin-4-amine (CNDR-51552) and 3-(methylamino)propan-1-ol. Yield: 10%
  • 1H-NMR (500 MHz; MeOD): δ 8.84 (m, 2H), 8.51-8.48 (m, 1H), 7.98 (t, J=6.5 Hz, 1H), 6.83 (m, 2H), 5.66 (m, 1H), 4.21 (t, J=5.7 Hz, 2H), 3.25 (t, J=7.4 Hz, 2H), 2.77 (s, 3H), 2.23 (m, 2H), 1.42 (d, J=7.0 Hz, 3H).
  • Figure US20170173016A1-20170622-C00118
    • 3-Chloro-5-(5-chlorothiophen-2-yl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine (CNDR-51566)
  • The title compound was prepared as described in Lamberth et al., Bioorg. Med. Chem. 2012, 20, 2803. The spectral data were identical to that reported in the literature.
  • 1H-NMR (500 MHz; CDCl3): δ 6.83 (d, J=3.8 Hz, 1H), 6.73-6.70 (m, 3H), 2.71 (s, 3H) ppm.
  • MS (ESI+) 374.97 [M+H+].
    • Microtubule Stabilization Assay
  • The HEK293 cell subclone, QBI293, was maintained in DMEM supplemented with 10% fetal calf or bovine serum, 1% penicillin/streptomycin antibiotic solution and 1% glutamine at 37° C. in 5% CO2. Cells were plated into 6-well plates at a density of 800,000 cells/well. Each plate had a well that contained the known microtubule stabilizer, epothilone D or cevipabulin, as a positive control and the remaining wells were used for compound evaluation. Test compounds were added at multiple concentrations to the test wells and incubated for 4 h. Subsequently, the media was removed and the cells were washed with 1 ml of ice-cold phosphate-buffered saline (PBS). After removal of PBS, 0.2 ml of ice-cold RIPA (0.5% sodium deoxycholate, 0.1% SDS, 1% NP-40, 5 mM EDTA, pH 8.0) containing protease inhibitor mix (1 μg/ml each of pepstatin, leupeptin, TLCK, TPCK and trypsin inhibitor), 1 mM PMSF and 1 M trichostatin A was added to the wells. The wells were then scraped using a cell scraper and pipetted into 1.5 ml microfuge tubes. The tubes were sonicated with a handheld sonicator at 20× on a power setting of 2, followed by centrifugation for 30 min at 15,000 rpm at 4° C. Supernatants were removed and quantified for protein concentration and the acetyl-tubulin levels were determined using an ELISA as described.
    • Acetyl-Tubulin ELISA
  • 384-well plates were coated with 12G10 α-tubulin antibody (Developmental Studies Hybridoma Bank at the University of Iowa; 10 μg/ml) in 30 μl of cold 0.1 M bicarbonate buffer. After overnight incubation at 4° C., the plates were washed with cold PBS, followed by the addition of Block-Ace solution and overnight incubation at 4° C. The blocking solution was removed and 10 μl of EC buffer (0.02 M sodium phosphate, pH 7.0, 2 mM EDTA, 0.4 M NaCl, 0.2% bovine serum albumin, 0.05% CHAPS, 0.4% BlockAce and 0.05% NaN3) was added to each well. Cell culture supernatants were diluted in EC buffer to final protein concentrations of 9, 3, 1.5 and 0.5 μg/30 μl, and 30 μl of each were added to wells in duplicate and plates were subsequently sealed. After overnight incubation at 4° C., the plates were aspirated and washed with cold PBS containing 0.05% Tween-20 and 0.05% thimerisol (PBS-Tween buffer), followed by addition of 30 μl/well of HRP-conjugated acetyl-tubulin antibody (6-11B-1 antibody from Sigma-Aldrich) that was prepared with a Peroxidase Labeling Kit following the manufacturer's instructions that was subsequently diluted 1:1000 in C buffer (0.02 M sodium phosphate, pH 7.0, 2 mM EDTA, 0.4 M NaCl, 1% bovine serum albumin and 0.05% thimerisol). The plates were incubated at room temperature for 4 h on a platform rocker, followed by washing with cold PBS-Tween buffer. Peroxidase substrate solution (30 μl) was added and the reaction was quenched after 5-10 min by addition of 30 μl of 10% phosphoric acid. Plates were read on a SpectraMax M5 plate reader at 450 nm. Because an acetyl-tubulin standard is not available, all data were normalized to a control treatment condition (e.g., no compound addition).
  • Results for preferred compounds of the invention are depicted in FIGS. 1-12 and Tables 5 and 6.
    • Acetyl Tubulin Immunofluorescence
  • The HEK293 cell subclone, QBI293, was plated onto poly-D-lysine-coated glass coverslips at 50,000 cells/ml in DMEM supplemented with 10% fetal calf or bovine serum, 1% penicillin/streptomycin antibiotic solution and 1% glutamine and maintained overnight at 37° C. in 5% CO2. The next day, cells were left untreated or were treated with 100 nM epothilone D, 100 nM CNDR-51533 or 1 μM colchicine. After an additional 4 h of incubation at 37° C. in 5% CO2, cells were washed twice with PBS, and then fixed for 15 min in PBS containing 4% paraformaldehyde. The cells were again washed twice with PBS, and permeabilized with 0.1% Triton X-100 in PBS for 15 min. Following the Triton X-100 treatment, the cells were washed twice in PBS, and treated with PBS containing 3% bovine serum albumin for 1 h. Acetyl-tubulin antibody was subsequently added (1:1000 dilution) and incubated for 1 h. Cells were then washed cells 3×5 min with 0.1% Triton X-100 in PBS, and secondary antibody (goat-anti-mouse labeled with Alexa fluor 488 at 1:1000) was added and allowed to incubate for 1 h. Upon completion of the antibody incubation, cells were washed 2×5 min with 0.1% Triton X-100 in PBS, followed by 15 min incubation with PBS containing DAPI (1:12000). Finally, the cells were washed once with PBS, followed by H2O, and the cover slips were mounted onto slides with Fluoromount G. Images were acquired on a microscope equipped for fluorescence detection. Each treatment was tested on three separate coverslips.
    • Determination of Plasma and Brain Compound Concentrations
  • Mouse brains were homogenized in 10 mM ammonium acetate, pH 5.7 (1:2; w/v) using a handheld sonic homogenizer. Mouse plasma was obtained from blood that was collected into a 1.5 ml tube containing 0.5M EDTA solution and which was centrifuged for 10 minutes at 4500 g at 4° C. Aliquots (50 μl) of brain homogenates (50% w/v in 100 mM NH4OAC pH 5.75) or plasma were mixed with 0.2 ml of acetonitrile, centrifuged at 15,000 g, and the resulting supernatant was used for subsequent LC-MS/MS analysis. The LC-MS/MS system was comprised of an Aquity UPLC and a TQ MS that was controlled using MassLynx software (Waters Corporation, Milford, Mass., USA). Compounds were detected using multiple reaction monitoring (MRM) of their specific collision-induced ion transitions. Samples were separated on an Aquity BEH C18 column (1.7 m, 2.1×50 mm) at 35° C. Operation was in positive electrospray ionization mode, with mobile phase A of 0.1% (v/v) formic acid, and B of acetonitrile with 0.1% (v/v) formic acid. Injections of 5 μl were separated at a flow rate of 0.6 mL/min using a gradient from 5% to 95% B over two minutes, followed by wash and re-equilibration steps. The MS was operated with a desolvation temperature of 450° C. and a source temperature of 150° C. Desolvation and source nitrogen gas flows were 900 L/hr and 50 L/hr, respectively. Source and MS/MS voltages were optimized for each compound using the MassLynx auto tune utility. To account for possible matrix effects on analytes, standard curves were generated for each compound from brain homogenate and plasma samples that had compound added at 24, 240, 2400 and 24000 nM. The standard curve samples were extracted and analyzed in an identical fashion as the corresponding tissue-derived samples, and peak areas were plotted against concentration and a linear regression curve was used to obtain estimated concentrations of the tissue-derived samples using the peak areas. In all cases, the tissue-derived sample peak areas fell within the linear portion of standard curves that were prepared and analyzed concurrently with the samples.
    • Determination of Brain Acetyl-Tubulin Levels
  • CD1 mice were administered vehicle (DMSO) or CNDR-51549 at multiple doses once per day for 3 days. Whole brain hemispheres were obtained from the mice, which were euthanized using protocols approved by the University of Pennsylvania Institutional Animal Care and Use Committee, and were homogenized and then briefly sonicated with a handheld sonicator in 1:5 (w/v) RIPA-INH buffer. The homogenates were centrifuged at 100,000×g for 30 min at 4° C., and the supernatants were collected. The supernatant samples were diluted before protein determination with a BCA assay. These supernatant samples were utilized in the Acetyl-Tubulin ELISA, as described above.
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Claims (24)

What is claimed:
1. A method of treating a neurodegenerative disease in a patient comprising administering to the patient a therapeutically effective amount of a compound of formula I:
Figure US20170173016A1-20170622-C00119
wherein
R1 is H, Cl, F, or Br;
R2 is C1-6alkyl or substituted C1-6alkyl;
R3 is H; or R2 and R3, together with the N atom to which they are attached, form a heterocycloC3-6alkyl;
R4 is H, Cl, F, or Br;
R5 is H, Cl, F, or Br;
R6 is F, Cl, Br, —N3, —OC1-6alkyl; —OC1-6alkyleneNR7R8, wherein R7 and R8 are each independently H or C1-6alkyl; and
R9 is pyridinyl, pyrimidyl, pyrazinyl, imidazolyl, pyrrolyl, pyrazolyl, quinolinyl, isoquinolinyl, thienyl, or furyl, each of which may be optionally substituted with one or more of F, Cl, Br, or C1-6alkyl;
or a stereochemical isomer thereof;
or a pharmaceutically acceptable salt thereof.
2. The method of claim 1, wherein R1 is Cl.
3. The method of claim 1, wherein R2 is C1-6alkyl.
4. The method of claim 3, wherein R2 is methyl, ethyl, propyl, or isopropyl.
5. The method of claim 1, wherein R2 is substituted C1-6alkyl.
6. The method of claim 5, wherein R2 is —CH(CH3)CF3
7. The method of claim 5, wherein R2 is —CH2CF3.
8. The method of claim 1, wherein R3 is H.
9. The method of claim 1, wherein R4 is F.
10. The method of claim 1, wherein R5 is F.
11. The method of claim 1, wherein R4 and R5 are each F.
12. The method of claim 1, wherein R6 is F.
13. The method of claim 1, wherein R6 is —OtBu.
14. The method of claim 1, wherein R6 is —OC1-6alkyleneNR7R8 and R7 and R8 are each C1-6alkyl.
15. The method of claim 14, wherein R6 is —O—CH2CH2CH2—N(CH3)2.
16. The method of claim 1, wherein R6 is —OC1-6alkyleneNR7R8; R7 is H; and R8 is C1-6alkyl.
17. The method of claim 16, wherein R6 is —O—CH2CH2CH2—NH(CH3).
18. The method of claim 1, wherein R9 is 2-pyridinyl, 2-pyrimidyl, 2-pyrazinyl, or 1-pyrazolyl.
19. The method of claim 1, wherein the compound of formula I is
Figure US20170173016A1-20170622-C00120
 X R1 R2 R3 R4 R5 R6 N Cl —CH(CH3)CF3 (S) H F F F N Cl —CH(CH3)CF3 (R) H F F F N Cl —CH(CH3)CF3 (S,R) H F F F N Cl H H F F F CH Cl —CH(CH3)CF3 (S) H F F F CH Cl —CH(CH3)CF3 (R) H F F F CH Cl —CH(CH3)CF3 (S,R) H F F F CH Cl H H F F F N Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2N(CH3)2 N Cl —CH(CH3)CF3 (R) H F F —OCH2CH2CH2N(CH3)2 N Cl —CH(CH3)CF3 (S,R) H F F —OCH2CH2CH2N(CH3)2 CH Cl H H F F —OCH2CH2CH2N(CH3)2 CH Cl H H F F —OtBu CH Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2N(CH3)2 CH Cl —CH(CH3)CF3 (S) H F F —OCH2CH2CH2NH(CH3)
20. The method of claim 1, wherein the compound of formula I is
Figure US20170173016A1-20170622-C00121
21. The method of claim 1, wherein the neurodegenerative disease is characterized by a tauopathy or compromised microtubule function in the brain of the patient.
22. The method of claim 1, wherein the neurodegenerative disease is Alzheimer's disease, frontotemporal lobar degeneration, Pick's disease, progressive supranuclear palsy (PSP), corticobasal degeneration, Parkinson's disease (PD), PD with dementia, Lewy body disease with dementia, or amyotrophic lateral sclerosis.
23. The method of claim 1, wherein the neurodegenerative disease is traumatic brain injury, in particular, repetitive traumatic brain injury and chronic traumatic encephalopathy, or post traumatic stress disorder.
24. The method of claim 1, wherein the neurodegenerative disease is schizophrenia.
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