AU2002225551B8 - Therapeutic chroman compounds - Google Patents
Therapeutic chroman compounds Download PDFInfo
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- AU2002225551B8 AU2002225551B8 AU2002225551A AU2002225551A AU2002225551B8 AU 2002225551 B8 AU2002225551 B8 AU 2002225551B8 AU 2002225551 A AU2002225551 A AU 2002225551A AU 2002225551 A AU2002225551 A AU 2002225551A AU 2002225551 B8 AU2002225551 B8 AU 2002225551B8
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- piperazin
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- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/22—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
- C07D311/24—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Description
WO 02/055014 PCT/SE02/00070 -1- THERAPEUTIC CHROMAN COMPOUNDS Field of the Invention This invention relates to novel 8-amino derivatives, methods for their preparation, pharmaceutical compositions containing them and their use in therapy.
Background of the Invention Serotonin (5-HT) has been implicated in many psychiatric disorders including but not limited to depression, generalized anxiety, eating disorders, dementia, panic disorder, and sleep disorders. Furthermore serotonin has been implicated in gastrointestinal disorders, cardiovascular regulation, motor disorders, endocrine disorders, vasospasm and sexual dysfunction. Serotonin receptors have been subdivided into at least 14 subtypes, see Barnes and Sharp, Neuropharmacology, 1999, 38, 1083-1152, incorporated herein by reference.
These various subtypes are responsible for serotonin's action in many pathophysicogical conditions. The 5-HT 1 family of receptors has high affinity for serotonin and consists of five related receptors. This family includes the 5-HTIB and 5-HTID receptor subtypes.
Compounds that interact with the 5-HTi family are known to have therapeutic potential in the above mentioned disorders and diseases. In particular, compounds that are 5HT1B and 5HT1D antagonist have been known to be antidepressant and anxiolytic agents. Compounds that are and 5HTID agonists have been used in the treatment of migraine.
Summary ofthe Invention Provided herein is a compound having the formula R6
RR
I 0 R 7
R
2 wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl; 005005043 -2- ;Z2 R 2is represented by (iii), or (iv) below: I NN
N
2 R (CH 2 0 RI R3 R 3 is independently at each position represented by optionally substituted C 1 6 alkyl, optionally substituted C 2 6 alkenyl, optionally substituted C 2 -6alkynyl, optionally substituted
C
3 6 CYCloalkyl or AOH;' n is 2, 3 or 4;- P is a heterocyclic ring; R R 6 is-H or methyl; Y is -CH2NH-A,
-C(=O)CH
2
-CH
2 -C("-O)-piperazine-,
CH
2
NA,
NACH
2 or a 5-membered heterocyclic.
R 7is a monocyclic or bicyclic aromatic ring or a heterocycleoptionally substituted by one or more substituents selected from R'-R 9 and R" wherein R 7 is connected to Y either by a single bond or by a ring fusion; R' is -CH 2
-SO
2
SO
2 NII-, a single bond as tether from R7 to or a five membered heterocyclic connected to R 7 byeither a single bond or by ring fusion; R9 is optionally substituted heterocycle, optionally substituted aryl, optionally substituted piperazinyl-RI 1, optionally substituted morpholinyl-RI 1 or optionally substituted thiomorpholinyl- or R1 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, C(=O)NEIA, C(=O)NA 2 or
OA;+
R" is alkyl, AOH, -SO 2 A, -SO 2
NH
2
-SD
2 NHA, -SO 2
NA
2 -SONHAR', -alkylR 9 C(0O)A, C(=O)NH 2 C&0)N{A, C(=O)NA 2 or or apharmaceutically acceptable salt of said compound.
In a further aspect of the present invention there is provided a compound represented by the formula 005005043 -2A-
SR
6 R1
I
R2 wherein Itn R' is, at each position, independently represented by hydrogen, optionally substituted CN alkyl, optionally substituted cycloalkyl, thiomethoxy, -NHA, -NA 2
-NHC(=O)A,
S 5 aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl;
R
2 is represented by
(CH
2 )n (i)
R
3
R
3 is independently at each position represented by optionally substituted Ci.6alkyl, optionally substituted C2-6alkenyl, optionally substituted C2- 6 alkynyl, optionally substituted C 3 6 cycloalkyl or AOH; n is 2, 3 or 4;
R
6 is -H or methyl; Y is CH 2
NH-,
2
-CH
2 -C(=O)-piperazine-, -CH 2
NA-,
-NACH
2 or a 5-membered heterocycle;
R
7 is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R 8
-R
9 and R'O, wherein R 7 is connected to Y either by a single bond or by a ring fusion; 005005043 2B R' is -Cl-I 2
-SO
2
-SO
2 NH-, a single bond as
O
0tether from R 7 to R 9 5-membered heterocycle connected to R 7 by a ring fusion or a single bond as tether;
SR
9 optionally substituted heterocycle, optionally substituted aryl, optionally substituted
C
5 piperazinyl-R", optionally substituted morpholinyl-R", optionally substituted thiomorpholinyl, or
R
1 0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, j halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, C(=O)NHA, C(=O)NA 2 or OA; cN R" is alkyl, AOH, -SO 2 A, -SO 2
NH
2
-SO
2 NHA, -SO 2
NA
2
-SO
2
NHAR
9
-C(=O)R
9 0 10 -alkylR 9
C(=O)NH
2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA; 0 or a pharmaceutically acceptable salt of said compound. The term "hydrocarbyl" refers to any structure comprising only carbon and hydrogen atoms up to 14 carbon atoms.
WO 02/055014 PCT/SE02/00070 -3- The term "alkyl" used alone or as a suffix or prefix, refers to straight or branched chain hydrocarbyl radicals comprising 1 to about 12 carbon atoms.
The term "alkenyl" refers to straight or branched chain hydrocarbyl radicals having at least one carbon-carbon double bond and comprising at least 2 up to about 12 carbon atoms.
The term "alkynyl" refers to straight or branched chain hydrocarbyl radicals having at least one carbon-carbon triple bond and comprising at least 2 up to about 12 carbon atoms.
The term "cycloalkyl" refers to ring-containing hydrocarbyl radicals comprising at least 3 up to about 12 carbon atoms.
The term "cycloalkenyl" refers to ring-containing hydrocarbyl radicals having at least one carbon-carbon double bond and comprising at least 3 up to about 12 carbon atoms.
The term "cycloalkynyl" refers to ring-containing hydrocarbyl radicals having at least one carbon-carbon triple bond and comprising about 7 up to about 12 carbon atoms.
The term "aromatic" refers to hydrocarbyl radicals having one or more polyunsaturated carbon rings having aromatic character, 4n 2 delocalized electrons) and comprising 6 up to about 14 carbon atoms.
The term "aryl" refers to aromatic radicals including both monocyclic aromatic radicals comprising 6 carbon atoms and polycyclic aromatic radicals comprising up to about 14 carbon atoms.
The term "alkylene" refers to divalent alkyl moieties, wherein said moiety serves to link two structures together.
The term "heterocycle" or "heterocyclic" or "heterocyclic moiety" refers to ringcontaining monovalent and divalent radicals having one or more heteroatoms, independently selected from N, O and S, as part of the ring structure and comprising at least 3 and up to about 20 atoms in the rings preferably 5 and 6 membered rings. Heterocyclic moieties may be saturated or unsaturated, containing one or more double bonds, and heterocyclic moieties may contain more than one ring.
The term "heteroaryl" refers to heterocyclic monovalent and divalent radicals having aromatic character.
Heterocyclic moieties include for example monocyclic moieties such as: aziridine, oxirane, thiirane, azetidine, oxetane, thietane, pyrrolidine, pyrroline, imidazolidine, pyrazolidine, dioxolane, sulfolane 2,3-dihydrofuran, 2,5-dihydrofuran tetrahydrofuran, thiophane, piperidine, 1,2,3,6-tetrahydro-pyridine, piperazine, morpholine, thiomorpholine, pyran, thiopyran, 2,3-dihydropyran, tetrahydropyran, 1,4-dihydropyridine, 1,4-dioxane, 1,3- WO 02/055014 PCT/SE02100070 -4dioxane, dioxane, homopiperidine, 2,3,4,7-tetrahydro-LH-azepine homopiperazine, 1,3dioxepane, 4,7-dihydro-1 ,3-dioxepin, and hexamethylene oxide. In addition heterocyclic moieties include heteroaryl rings such as: pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, thienyl, furyl, pyrrolyl, imidazolyl, thiazolyl, oxazolyl, pyrazolyl, isothiazolyl, isoxazolyl, 1 ,2,3-triazolyl, tetrazolyl, 1 ,2,3-thiadiazolyl, 1 ,2,3-oxadiazolyl, 1,2,4-triazolyl, 1,2,4thiadiazolyl, 1 ,2,4-oxadiazolyl, I ,3,4-triazolyl, 1 ,3,4-thiadiazolyl, and 1,3,4 oxadiazolyl;* Additionally, heterocyclic moieties encompass polycyclic moieties such as: indole, in doline, quinoline, tetrahydroquinoline, isoquinoline, tetrahydroisoquinoline, 1 ,4-benzodioxan, coumarin, dihydrocoumarin, berizofuran, 2,3 -dihydrobenzofuran, 1 ,2-benzisoxazole, bonzothiophene, benzoxazole, benzthiazole, benzimidazole, benztriazole, thioxanthine, earbazole, carboline, acridine, pyrolizidine, and quinolizidine.
In addition to the polycyclic heterocycles described above, heterocyclic moieties include polycyclic heterocyclic moieties wherein the ring fusion between two or more rings comprises more than one bond common to both rings and more than two atoms common to both rings. Examples of such bridged heterocycles include quinuclidine, diazabicyclo[2.2. 1]heptane and 7-oxabicyelo[2.2. 1]heptane.
The term "halo" or "halogen" refers to fluorine, chlorine, bromine and iodine radicals.
The term,"alkoxy" refers to radicals of the general formula wherein R is selected from a hydrocarbyl radical. Alkoxy moieties include methoxy, ethoxy, propoxy, isopropoxy, butoxy, t-butoxy, isobutoxy, cyclopropylmethoxy, allyloxy, and prop argyloxy..
The term amine or amino refers to radicals of the general formula -NRR', wherein R and R' are independently selected from hydrogen or a hyckocarby radical.
Detailed Description of the Invention In a further aspect of the invention, A, R' and R 3 each independently, as an alkyl, alkenyl, alkynyl and as a cycloalkyl, may optionally be substituted with halogen, nitro, cyano, hydroxy, trifluoromethyl, amino, carboxy, carboxamido, amidino, carbamoyl, mercapto, sulfamoyl, C 1 4 ailkyl, C2-4 alkenyl, C 2 4 alkynyl, C3.6 cycloalkyl, C 3 6 cycloalkenyl, C 14 alkoxy, C1-4 alkanoyl, C 1 4 alkanoyloxy, N-(C 14 alkyl), N(CI- 4 alkyl) 2 C1-4 alkanoylamino, (C 1- alkanoYl) 2 aMino,'N-(C 1 4 alkyl)carbamoyl, N,N-(C 1 4 alkyl)2carbamoyl, (C 1 4
(C
1 4 alkyl)S(O), (CI- 4 allcyl)S(O) 2
(C-
4 alkoxycarbonyl, N-(C, 4 alkyl)sulfamoyl, NN-C 1 4 alkyl)sulfamoyl, C 1 4 alkylsolfonylamino, and heterocyclic.
Examples of optional substituents for aryl and heterocyclic groups, when not otherwise defined, are halogen, nitro, cyano, hydroxy, trifluoromethyl, amino, carboxy, WO 02/055014 PCT/SE02/00070 carboxamido, amidino, carbamoyl, mercapto, sulfamoyl, C 14 alkyl, C 2 4 alkenyl, C 2 4 alkynyl, C3-6 cycloalkyl, C 3 6 cycloalkenyl, C 14 alkoxy, C 1 4 alkanoyl, C 14 alkanoyloxy, N-(C1- 4 alkyl), N(C1- 4 alkyl) 2
C
14 alkanoylamino, (C 1 4 alkanoyl) 2 amino, N-(C 1 4 alkyl)carbamoyl, N,N-(CI-4 alkyl) 2 carbamoyl, (C 1 4
(C
1
I
4 alkyl)S(O), (C 1 4 alkyl)S(0)2, alkoxycarbonyl, N-(C 1 -4 alkyl)sulfamoyl, N,N-C 14 alkyl)sulfamoyl, C 14 alkylsolfonylamino, and heterocyclic.
A, R 1 and R3 each independently as an alkyl, alkenyl or alkynyl may be straight or branched, preferably having 1-6 carbon atoms. A, R' and R3 preferably have 3-6 atoms when each are independently a cyclic alkyl. Other preferable values for A, R' and R3 when each are an alkyl, include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, cyclopentyl, neopentyl and cyclohexyl. Preferable values for R' when R' is a halogen are fluorine, chlorine, and bromine. Other preferable values for R' when R' is at position 6 on the bicyclic ring are methyl, ethyl, ethoxy and methoxy. Preferable values for R when R' is at position 5 on the bicyclic ring are methyl, ethyl and methoxy. When R' is at position on the bicyclic ring, R' is more preferably When R 1 is at position 7- on the bicyclic ring, R' is preferably -H.
R2 is preferably represented by Formula i. Preferably R2 is represented by formula i, wherein n equals 2. Most preferably R2 is represented by N-methyl piperazinyl.
R
3 is preferably represented by hydrogen, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, and tert-butyl. R 3 is most preferably represented by methyl.
R4 is preferably represented by hydrogen, methyl, ethyl, n-propyl, isopropyl and trimethylsilanyl-ethoxymethoxy. R4 is most preferably represented by methyl.
R6 is preferably represented by H.
Y represents a linking group. Y is preferably -C(=O)N(CH 3 when Y is Y may also be -C(=O)-piperazine. When Y represents a five-membered heterocyclic ring, Y may be represented by, for example, pyrrole, thiophene, furan, imidazole, thiazole, oxazole, pyrazole, isothiazole, isoxazole, 1,2,3-triazole, 1,2,3-thiadiazole, 1,2,3oxadiazole, 1,2,4-triazole, 1,2,4-thiadiazole, 1,2,4-oxadiazole, 1,3,4-triazole, 1,3,4-thiadiazole or 1,3,4-oxadiazole.
More preferably, Y is Examples of R7 that represent monocyclic or bicyclic aromatic ring or a heterocycle include, but are not limited to, phenyl; 1- and 2-naphthyl; 3- and 4-pyridyl; 2- and 3thienyl; 2- and 3-furyl; 2- and 3-pyrrolyl; imidazolyl; thiazolyl; oxazolyl;pyrazolyl; isothiazolyl; isoxazolyl; 1,2,3-triazolyl; 1,2,3-thiadiazolyl; 1,2,3-oxadiazolyl; 1,2,4-triazolyl; WO 02/055014 PCT/SE02/00070 -6- 1 ,2,4-thiadiazolyl; 1 ,2,4-oxadiazolyl; 1,3 ,4-triazolyl; 1,3 ,4-thiadiazolyl; 1,3,4 oxadiazolyl; quinolyl; isoquinolyl; indolyl; benzothienyl; benzofuryl; benzimidazolyl; benzthiazolyl; benzoxazolyl; or triazinyl.
R7may also b e represented by the Formula R7may further be represented by the Formula (vi): R'(vi) When the values for R 7 are as set forth above, R 8 may be a single bond as tether,
-CH
2
-SO
2
-SO
2 or a five membered heterocycle connected to R 7 by single bond or by a ring fusion; and R 9 may represent an aryl, heterocyclic or heteroaryl each independently optionally substituted with halogen, nitro, cyano, hydroxy, trifluoromethyl, amino, carboxy, carbamoyl, mercapto, sulfamoyl, C 14 alkyl,
C
24 alkenyl, C2_ alkynyl, C 3 6 cycloalkyl, C 3 6 cycloallcenyl, CI- 4 alkoxy, C14 alkanoyl, C 14 alkanoyloxy, N-(C 1 4 alkyl), N(C 14 alkyl) 2 CI- alkanoylamino, (CI- 4 alkanoyl) 2 amino, N-(C 1 4 a~kyl)carbamoyl, N,N-(Cj- 4 2 carbamoyl, C 1 4 Cr4S(O), (C, 4 alkyl)S(=O) 2
(C
14 alkoxycarbonyl, N-(C 1 -4 alkyl)sulfamoyl, N,N-C 1 .4 alkyl)sulfamnoyl,, C 1 alkylsolfonylamino, or heterocyclic. Preferably R 9 is an optionally substituted-heterocyclic moiety.
More preferably R 9 represents piperazine, thiomorpholine or morpholine each independently optionally substituted on carbon with at least one substituent selected from A.
R
8 may be a five membered heterocycle, incorporating at least one heteroatom selected from N, 0, or S and it may be connected to R 7 by a. ring fusion, preferably when R 7 is phenyl.
When RS is a single bond as tether, R 9 is preferably methoxy, cyano, a five-membered heterocycle optionally substituted with at least one substituent represented by A or R, 1 for example compounds represented by the Formulas (vii), (viii) and (ix): N N R(vii) WO 02/055014 PCT/SE02/00070 -7- N O-R (viii) N S-R (vii) When R 8 is represented by a 5-membered heterocyclic comprising N and further when it is connected to R 7 by a ring fusion, R 9 is preferably attached at the nitrogen atom.
R
9 is most preferably -C(=O)CH 2 CH3.
When R 7 is phenyl or a 6-membered heterocyclic ring, R 9 is attached via the R 8 tether at the 3- or 4-position of the phenyl or a 6-membered heterocyclic ring. Preferably, R 9 is attached via the R 8 tether at the 3- or 4-position of the phenyl or a 6-membered heterocyclic ring. More preferably, R 9 is attached via the R 8 tether at the 4 position of the phenyl or a 6membered heterocyclic ring.
R
1 may be represented by alkyl or cycloalkyl each independently optionally substituted with halogen, nitro, cyano, hydroxy, trifluoromethyl, amino, carboxy, carbamoyl, mercapto, sulfamoyl, C-4 alkyl, C 2 4 alkenyl, C 2 4 alkynyl, C 3 -6 cycloalkyl, C 3 -6 cycloalkenyl, C1- 4 alkoxy, C1- 4 alkanoyl, C 14 alkanoyloxy, N-(Cl- 4 alkyl), N(C1- 4 alkyl) 2
C
1 4 alkanoylamino, (C1-4 alkanoyl) 2 amino, N-(C1-4alkyl)carbamoyl, N,N-(C 14 2 carbamoyl, C 14
)S,
C1- 4 (C1 4 alkyl)S(0) 2
(C
14 alkoxycarbonyl, N-(C-4 alkyl)sulfamoyl, N,N-C.4 alkyl)sulfamoyl, C-4 alkylsulfonylamino, or heterocyclic. R 10 is preferably a halogen, preferably chlorine or fluorine, cyano, or -OCH 3 When R' 1 is a halogen it is preferably chlorine or fluorine. When R 7 is a phenyl or 6-membered heteroaromatic ring, R 1 0 is attached at the 3- or 4-position of the phenyl or a 6-membered heterocyclic ring.
Preferably, R' 1 is attached at the 2- or 3-position of the phenyl or a 6-membered heterocyclic ring when R 9 is attached via the R 8 tether at the 4-position of the phenyl or a 6-membered heterocyclic ring. More preferably, R' 1 is attached at the 3-position of the phenyl or a 6membered heterocyclic ring when R 9 is attached via the R 8 tether at the 4-position of the phenyl or a 6-membered heterocyclic ring.
WO 02/055014 PCT/SE02/00070 -8- When R 8 is represented by a single bond as tether, R 9 is preferably represented by an optionally substituted heterocyclic, optionally substituted on carbon with at least one substituent selected from A and further substituted on a heteroatom opposite to the heteroatom attached to the tether, with a substituent represented by R 11 (see Formulas (vii), (viii) and The preferred heterocyclic compounds for R8 are piperazine, morpholine, or thiomorpholine When R 1 represents SO z A it is preferably represented by an alkylsufonyl, more preferably -SO 2
CH
3
-SO
2
CH
2
CH
3
SO
2 -n-C 3 H, SO2-i-C 3
H
7 SO2-n-C 4 Hlo, -SO2-i-C 4 Ho, or-
SO
2 -t-C 4 Hio. When R 11 represent it is preferably represented by an alkylcarbonyl more preferably -C(=O)CH 3
-C(=O)CH
2
CH
3 C(=O)-n-C 4 Hio, 4 Hlo,
C
4
H
10 or -C(=O)C 3
H
7 When R 11 is represented by C(=O)NHA or C(=O)NA 2 it is preferably an alkyl or dialkyl carbamoyl more preferably C(=O)NCH 2
CH
3 C(=O)NH-cycloC 6
H
2 or C(=O)NH-cycloC s Hio,. When R" is represented by C(=O)R 9 it is preferably pyrrolidine, or -C(=O)-morpholine. When is represented by S02NA 2 it is preferably
SO
2
N(CH
3 2 When R" is represented by AOH, it is preferably represented by, CHzCH 2
OH
or -C(=O)CH 2
CH
2 OH. R" may also be represented by -C(=O)OC 4 HIo.
In preferred embodiments, when Y is represented by -C(-O)NH:
R
1 is halogen or methoxy, most preferably fluorine, at the 6 th position of the bicyclic ring, and is preferably hydrogen, methyl, ethyl or methoxy at the 5 t h position of the bicyclic ring, and is hydrogen at the 7 th position on the bicyclic ring;
R
2 is methyl piperazine;
R
6 is hydrogen;
R
7 is phenyl substituted with R8-R9
R
8 is a single bond as tether;
R
9 is a heterocyclic moiety, preferably morpholine or piperazine attached to R 8 by nitrogen and optionally substituted on the other nitrogen (for piperazine) with R' 1 or optionally substituted on the oxygen with R 11 when R 9 is morpholine; R" is AOH or -SO 2 A wherein A is represented by methyl or ethyl.
The compounds provided herein are useful in the form as a free base, but may also be provided in the form of a pharmaceutically acceptable salt, and/or in the form of a pharmaceutically acceptable hydrate. For example pharmaceutically acceptable salts of compounds of Formula I, include those derived from mineral acids such as for example: WO 02/055014 PCT/SE02/00070 -9hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, hydrobromic acid, hydroiodic acid, nitrous acid, and phosphorous acid. Pharmaceutically acceptable salts may also be developed with organic acids including aliphatic mono and dicarboxylates and aromatic acids.
Other pharmaceutically-acceptable salts of compounds of the present invention include for example hydrochloride, sulfate, pyrosulfate, bisulfate, bisulfite, nitrate, and phosphate.
Processes for the manufacture of the compounds of Formula I are provided as further features of the invention. Many of the Compounds described herein can be made by processes known in the chemical arts for the production of structurally analogous compounds.
Accordingly, the compounds of this invention may be prepared by employing procedures known in the literature starting from known compounds or readily prepared intermediates. For example, the core bicyclic, heterocyclic structure may be made by first preparing a chromone, quinolone or quinoline. For compounds of the present invention that have Y as an amide linker, the compounds are preferably made by the general procedure for amide coupling, that is by coupling an anime with an acid hydrochloride. The amines used in the current invention if not commercially available may be made by known techniques. For example as a first step in the process of making compound of Formula I, a nitro compound may be reduced to an amine. The nitro compound may be a nitrophenyl compound. The resulting amines may be .reacted with an acid hydrochloride Provided herein is a process for preparation of a precursor compound or use in practicing aspects of the present invention by reacting a compound of Formula (VIa):
XH
Halogen Via
R
2
R
3 and R 7 are as defined for Formula I unless otherwise specified and X is represented by with for example a compound represented by:: R'O2C -C2R' S, wherein R' is represented by alkyl, preferably lower alkyl C1-C 6 most preferably methyl or ethyl, to form a precursor compound of Formula (VIb): WO 02/055014 PCT/SE02/00070
CO
2
R'
x0 2
R'
R1 X Q 02R' Halogen Vlb R' is preferably fluorine, chlorine, methyl, methoxy, ethoxy or hydrogen. The Halogen is preferably Chlorine or Bromine. The reaction may be carried out in the presence of a catalyst such as tetrabultyammonium fluoride in THF. The reaction may be stirred for example at room temperature and refluxed with heat.
Further provided herein is a process for the preparation of a precursor compound comprising hydrolyzing the esters of compound (VIb) to form intermediate (VIc):
,CO
2
H
*C0 2
H
Ilogen Vic This reaction may be carried our for example by reacting a compound of Formula (VIb) with a base such as sodium hydroxide (aqueous). Also provided here is a process for the preparation of an intermediate by the cyclization of compound (VIc) to form intermediate (VId) WO 02/055014 PCT/SE02/00070 -11- 0
OR"
Halogen 0 VId Intermediate compound (VId) may be formed by refluxing a compound of Formula (Vie) with a strong acid H 2 SO) and further refluxed with heat and an alkyl alcohol for example R"OH wherein R" is CI-C 4 alkyl, preferably ethyl.
In an additional aspect of the invention, a process is provided for the preparation of an intermediate by reacting a compound of Formula (VId) with an amine of R 2 in the presence of a catalyst and a base to form intermediate Formula (VIe): 0 Ri I
<N
R
2 0 Vie In a further embodiment of the invention, a compound of Formula (VId) is reacted with a catalyst selected from the group consisting of nickel and palladium. Preferably the palladium is provided in the presence of a phosphine ligand for example 2,2'-bis(diphenylphosphino)- 1,1 '-binapthyl. The palladium may be provided as tris(dibenzylideneacetone) dipalladium.
The base is preferably selected from the group consisting of potassium carbonate, sodium carbonate, cesium carbonate and triethylamine and mixtures thereof.
Further provided herein is an acid hydrochloride of a compound of Formula (VIe) which is intermediate Formula (VIf): WO 02/055014 PCT/SE02/00070 -12- 0 X OH
R
2 0
HCI
Vlf The intermediate Formula (VIf) may be formed for example by heating a compound of Formula (VIe) in the presence of an acid and water HCL/H 2 0).
In another aspect of the invention provided is intermediate Formula (VIg): 0
R'
R
2 0
HCI
WO 02/055014 PCT/SE02/00070 13 Thus, in another aspect of the invention, a leaving group is added to the carboxylate of a compound of Formula (VIf). L is a leaving group. This intermediate is useful in that the acid is activated to provide an electrophile. L is preferably represented by chlorine in intermediate Formula (VIg) which is prepared by reacting a compound of Formula (VIf) with thionyl chloride (SOC2).
Provided herein is a compound of Formula (VIh): 0 R1 H X R R2 VIh Methods for reacting amines with acid chlorides may be used to prepare compounds of formula I such as a compound of Formula (VIh) For example, a method for the preparation of (VIh) may include reacting a compound of Formula (VIg) with H 2
N-R
7 in the presence of
DIPEA.
Alternatively, compounds of Formula (VIh) may also be prepared by reacting a compound of Formula (VIf) with H 2
N-R
7 in the presence for example 1hydroxybenzotriazole (HOBT), O-(1H-Benzotriazol-l-yl)-N,N,N'N'-pentamethyleneuronium tetrafluorborate (TBTU), and (dimethylamino)pyridine, preferably in that order.
Compounds of Formulas (VIe), (VIf), and (VIg), and (VIh) may also comprise a pharmaceutically acceptable salt of said compounds.
The compounds and processes above may also be used to prepare the chroman derivatives of Formula via the saturation of the double bond (4H-chromene) in the bicyclic 005005043 -14- 0 compound. Depending on the reduction conditions, the 4-oxo derivative may or may not be C obtained.
SFurther provided is a compound of Formula (VIfl): i) R 2
O
C HCI Vlfl wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkenyl;
R
2 is represented by
N
(CH
2 )n N (i)
R
3
R
3 is independently at each position represented by optionally substituted Ci-6alkyl, optionally substituted C 2 6 alkenyl, optionally substituted C2-6alkynyl, optionally substituted C 3 6 cycloalkyl or AOH; n is 2, 3 or 4; and X is represented by O; or a pharmaceutically acceptable salt thereof.
The compound of Formula (VIfl) may be formed for example by heating a compound of Formula (VIe) 005005043
O
R
2
O
Vie wherein R1 is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkenyl;
R
2 is represented by
S/(
(N
N (i)
R
3
R
3 is independently at each position represented by optionally substituted C 1 6 alkyl, optionally substituted C 2 .6alkenyl, optionally substituted C 2 -6alkynyl, optionally substituted C 3 6 cycloalkyl or AOH; n is 2, 3 or4; and in R is CI-C 4 alkyl; in the presence of an acid and water to form a mixture wherein the mixture is hydrogenated using a catalyst. In a more particular embodiment, a palladium catalyst is used.
In another embodiment, provided herein is a compound of Formula (VIgl) 005005043 16- R1 (N
R
1
SR
2
O
HCI
SVIgl c wherein R is, at each position, independently represented by hydrogen, optionally
O
N substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl; L represents a leaving group;
R
2 is represented by
N
(CH
2 )n N (i)
R
3
R
3 is independently at each position represented by optionally substituted Ci.
6 alkyl, optionally substituted C 2 6 alkenyl, optionally substituted C2-6alkynyl, optionally substituted C3- 6 cycloalkyl or AOH; n is 2,3 or 4; and X is represented by O; or a pharmaceutically acceptable salt thereof.
005005043 17- The compound Formula (VIgl) may be formed for example by replacing the hydroxyl group of the carboxylate moiety of Formula (VIfl) with a leaving group.
In another embodiment, provided herein is a compound of Formula (VIh X R7 In 0R 2
O
VIh1 wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl;
R
2 is represented by
N
(CH
2 )n N (i)
R
3 R is independently at each position represented by optionally substituted CI.
6 alkyl, optionally substituted C 2 _6alkenyl, optionally substituted C2-6alkynyl, optionally substituted C3_6cycloalkyl or AOH; n is 2, 3 or 4; R is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R -R 9 and R 0 005005043 17A- O R is -CH 2
-SO
2
-SO
2 NH-, a five membered heterocycle connected to R 7 by a ring fusion or single bond as tether; ;Z 9
R
9 is morpholine optionally substituted with at least one substituent selected from A, thiomorpholino, piperazine-R", optionally substituted aryl, optionally substituted heterocyclyl, or -C(=O)CA;
IR'
0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, 1" cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, -C(=O)NHA, C- -C(=O)NA 2 or OA; SR" is alkyl, AOH, -SO 2 A, -SO 2
NH
2
-SO
2 NHA, -SO 2
NA
2
-SO
2
NHAR
9
-C(=O)R
9 -alkylR 9
C(=O)NH
2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA.
and X is represented by O; or a pharmaceutically acceptable salt thereof.
The compound Formula (VIhl) may be formed for example by reacting a compound of formula (VIfl) with H 2 NR wherein R 7 is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R 8
R
9 and R 1 0
R
8 is -CH 2 -SO2-, -SO 2 NH-, a five membered heterocycle connected to R 7 by a ring fusion or single bond as tether;
R
9 is morpholine optionally substituted with at least one substituent selected from A, thiomorpholine, piperazine-R", optionally substituted aryl, optionally substituted heterocyclic, or -C(=O)CA;
R
1 0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, -C(=O)NHA,
-C(=O)NA
2 or OA; R" is alkyl, AOH, -S0 2 A, -SO 2
NH
2
-SO
2 NHA, -SO 2
NA
2 -S02NHAR 9
-C(=O)R
9 -alkylR 9
C(=O)NH
2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA.
In another embodiment, the compound Formula (Vlhl) may be formed for example by reacting a compound of Formula (Vlgl) with H 2
NR
7 wherein R 7 is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R-R 9 and R 1 0
R
8 is -CH 2 -S02-, -SO 2 NH-, a five membered heterocycle connected to R 7 by a ring fusion or single bond as tether; 005102365 -17B-
R
9 is morpholine optionally substituted with at least one substituent selected from A, thiomorpholine, piperazine-R", optionally substituted aryl, optionally substituted heterocyclic, or -C(=O)CA;
R'
1 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, -C(=O)NHA,
-C(=O)NA
2 or OA; R" is alkyl, AOH, -SO 2 A, -SO 2
NH
2
-SO
2 NHA, -SO 2
NA
2
-SO
2
NHAR
9
-C(=O)R
9 -alkylR 9
C(=O)NH
2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA.
In another embodiment, provided herein is a compound of the Formula or a pharmaceutically acceptable salt thereof, and/or a tautomer thereof, and/or a hydrate thereof, and/or a solvate thereof, and/or a steroisomer thereof.
In another embodiment, provided herein is a compound of the Formula or a pharmaceutically acceptable salt thereof, and/or a tautomer thereof, and/or a hydrate thereof, and/or a solvate thereof, and/or a steroisomer thereof.
A method for preparing the acid hydrochlorides useful in synthesis of a chromone is set forth in Scheme 1 below.
004592832 18 THIS IS A BLANK PAGE THE NEXT PAGE OF THE SPECIFICATION IS PAGE 19 WO 02/055014 PCT/SE02/00070 19 iN N 00 2 R'00R OH BrR
(R
1 q Hal~~ogen O RH. OH 3
C
2 1- 5 0 5 j02R'
R',-OCH
3 F, OH 3 Cl, OtH.Vib Via NaOH 002 RC 1 1. H 2 S0 4
R
1 gen2. EtCH, refiux 0ge Vid H N VIC
C(CH
2 )n (Or precursor amines for (ii) or (iii)' N- structural variations of R 2 X R3 Pd catalyst phosphine iigand #cesium carbonate 0 a0 R1+
HCI/H
2 0 0OEt 0OH N"CH2. 0.
N
(CHH2)n N C' HO N l Vie Vif Scheme 1: Preparation of chromone-2-carboxylic acids as intermediates in the synthesis of compounds -of the present invention.
Alternatively, the chromone-2-carboxylic acid may be converted to the acid chloride and reacted immediately with an appropriate amine, as depicted in Scheme 2, below: WO 02/055014 WO 02/55014PCT/SE02/00070 SOC1 2
TBTUHB
DMF, DJPEA Scheme 2. Amide synthesis via acid chloride intermediate.
Additional functional group manipulations include, but are not limited to, 0dealkylation and N-dealkylation (Scheme 3).
WO 02/055014 WO 02/55014PCT/SE02/00070 -21- 0
H
3
H
0 I H BBr 3 at CN)o> N> Example 31 0 Ur1 3 Example 86 I -chloroethyl chioroformate 64% Example Scheme 3: Functional group manipulation with compounds of the present invention includes, but is not limited to, N- and 0- dealkylation Quinoline and quinolone compounds of the present invention are prepared and derivatized via synthetic routes similar to those employed for synthesis of the chromone-2carboxamides described above and in Schemes 1-3. These synthetic routes to quinoline and WO 02/055014 PCT/SE02/00070 -22quinolone compounds of the present invention are depicted in Scheme 4, infra.
R
Br R1=OCH 3 or F MeO 0 MeO' 0 methanol reflux 0 N H OMe Br H 0 1230o0 NaH' N OMe 2-(trimethylsilyl)ethoxy_ N methyl chloride Br j 0 amine, PdI 0
N
Br H 0 R1 0 amnineN OMe1 e
OH~
NLiOH N OMe -amine, Pd R 0 THF/McOH/H 2 0 R 2 0 amine
TBTU
HOBt IOeci I-Z 1 Nk N R NHrq~ CI oxalyl chloride N Br 0 1) amine
CI
N R R N NHAr amine N A, Br 0 amine, Pd .NHIAr
R
N1- N NHAr R 2 0 amine
TBTU
HOBt -NHAr .NHAr 6 amnine, Pd Hi 2-(trimethylsilyl)ethoxy- 0 methyl chloride WO 02/055014 PCT/SE02/00070 23 It will be appreciated by those skilled in the art that certain compounds of the present invention contain for example asymmetrically substituted carbon and/or sulfur atoms, and accordingly may exist in and be isolated in, optically-active and racemic forms. It will be appreciated by those skilled in the art.that certain compounds of the present invention contain for example asymmetrically substituted carbon and/or sulfur atoms, and accordingly may exist in and be isolated in, optically-active and racemic forms. Some compounds may exhibit polymorphism, thus it is to be understood that the present invention encompasses racemic, optically-active, polymorphic or stereoisomeric forms, or mixtures thereof, which forms possess properties useful in the treatment of the disorders set forth below. Preparation of optically active forms is well known in the art how (for example by resolution of racemic forms by recrystallization techniques, synthesis from optically-active starting materials, chiral synthesis, or by chromatographic separation using a chiral stationary phase) and how to determine efficacy for the treatment of the disorder described above.
Compounds of Formula I have been found to be 5-HT1B and 5HT1D agonists. The compounds of Formula I, and their pharmaceutically acceptable salts, may also be used in a method for the treatment of migraine.' The treatment of this disorder comprises administering to a warm-blooded animal, preferably a mammal, more preferably a human, in need of such treatment, an effective amount of a compound of Formula I or a pharmaceutically acceptable salt of said compound.
Further provided is the use of a compound of Formula I in the preparation of a medicament for the treatment of a disorder such as migraine in a warm-blooded animal, preferably a mammal, more preferably a human, suffering from such disorder.
The invention further provides a pharmaceutical composition suitable for the treatment of the above describe disorders comprising administering to a warm-blooded animal having such disorder an effective amount of a pharmaceutical composition of a compound of Formula I, or a pharmaceutically acceptable salt.
The invention also provides a pharmaceutical composition comprising a compound of Formula I, as defined herein, or a pharmaceutically acceptable salt, in combination with a pharmaceutically acceptable carrier. Preferred compounds of Formula I, for use in the compositions of the invention are as described above.
All compounds described herein demonstrate binding affinities (observed Ki values), in an assay described below, of less than about 10M. Further, compounds of the present WO 02/055014 PCT/SE02/00070 24 invention not only demonstrate 5HTIB antagonist activity by reversing 5HTIe agonist-induced hypothermia in the guinea pig, these compounds are considered to be orally active, and hence, they are the preferred compounds. Examples 1, 10, 11, 31, 32, 34, 44, 55, 56, 57, 71 and 72, infra, demontrate 5HT1B antagonist activity in a dosage range of 0.006-5.5 mg/kg. In addition, compounds described herein demonstrate activity in the learned helplessness assay for antidepressant/antianxiety activity. Examples 31, 44, 71 and 72, infra, demonstrate activity in the learned helplessness assay. In addition, compounds were tested for maximal intrinsic activity and were found to have measured IA's of negative 50% to positive 150% in the GTPyS assay described below, thus demonstrating a range of response from agonism (low percentages) to antagonism (high percentages).
The compounds described herein may be provided or delivered in a form suitable for oral use, for example in a tablet, lozenge, hard and soft capsule, aqueous solution, oily solution, emulsion, and suspension. The compounds may be also be provided for topical administration, for example, as a cream, ointment, gel, spray, or aqueous solutions, oily solutions, emulsions or suspensions. The compounds described herein may also be provided in a form suitable for nasal administration for example, as a nasal spray, nasal drops, or dry powder. The compositions may also be administered to the vagina or rectum in the form of a suppository. The compounds described herein may also be administered parentally, for example by intravenous, intravesicular, subcutaneous, or intramuscular injection or infusion.
The compounds may be administered by insufflation (for example as a finely divided powder). The compounds may also be administered transdermally or sublingually.
The compounds of the invention may accordingly be obtained by conventional.
procedures using conventional pharmaceutical excipients, well known in the art. Thus, compositions intended for oral use may contain, for example, one or more coloring, sweetening, flavoring and/or preservative agents.
The amount of active ingredient that is combined with one or more excipients to produce a single dosage form will necessarily vary depending upon the host treated and the particular route of administration. The size of the dose for therapeutic or prophylactic purposes of a compound of the Formula I, will naturally vary according to the nature and severity of the conditions, the age and sex of the animal or patient and the route of administration, according to well known principles of medicine. Various assays and in vivo tests are known for determining the utility of the compounds in the disorders noted above and specifically as agonists and antagonists of 5HTIB and 5HT1D WO 02/055014 PCT/SE02/00070 The utility of the compounds for example to treat depression may be shown via a learned helplessness test in guinea pigs, which is used extensively as correlative to antidepressant activity in humans. The learned helplessness test may be carried out as follows: Seventy male Hartley guinea pigs, each weighing about 350-425 gm are fed ad lib, and are housed under a 12-hour light/dark cycle. The procedure consists of two phases: The induction phase and the avoidance training phase. In the induction phase, subjects are placed into standard shuttle cages (20 L X 16 W X 21 centimeters H) which are fitted with a grid floor.
Electrical stimulation (1.25 mA, 10 sec duration) is delivered to the floor of the cage every during 1 hour daily sessions. Subjects have no opportunity to escape or to avoid shocks. Induction is conducted for 2 consecutive days.
In avoidance training, testing is also conducted in the shuttle cages, except that the subjects are not returned to the same chamber in which induction had occurred. Additionally, all cages are fitted with a partition with an arch in the center of the cage, through which animals can pass between the left and right halves of the cage. The procedure employed is a standard shuttle avoidance procedure in which a compound, conditioned stimulus (a presentation of a tone and turning on of a lamp on the side of the cage that the guinea pig was occupying) serves to indicate presentation of electrical current to the floor of the cage. Shock is presented for a 5 sec period, 5 sec after initiation of the conditioned stimulus. Entry into the opposite side of the shuttle cage via the arched partition prior to shock onset results in the end of the trial (avoidance response). If shock is delivered, entry into the opposite side of the cage results in termination of the shock and CS (escape). Reversal of learned helplessness in the induction subjects correlates to antidepressant activity of the test compound.
Avoidance training, 45-min in duration, is conducted on 2 consecutive days, beginning 48 hr after the final induction session. Seventy subjects are assigned to 1 of 6 groups of 11-12 animals. The groups are as follows: 1) No induction group. The subjects are placed into the shuttle cages but are not given inescapable shock, the animals are subsequently- trained in the avoidance procedure and the vehicle is administered; 2) Induction vehicle control group; 3) Imipramine 17.8 mg/kg; 4) 0.3 mg/kg compounds; 1 mg/kg compounds; and 6) 5 mg/kg compounds.
WO 02/055014 PCT/SE02/00070 -26- Groups 2-6 are given induction and avoidance training sessions. Injections are administered immediately following induction sessions and 1 hour prior to avoidance training sessions. A second injection is administered 7-8 hours following the first injection, for a total of 9 injections administered over 5 days. No injections are administered following the final avoidance training session.
Compounds of the present invention may be administered in a volume of 1mL/kg bwt.
Imipramine is dissolved in DI water. The compounds are dissolved in DI water, to which was added a few drops of lactic acid (pH The vehicle control is DI water prepared with lactic acid to the same pH as the-treated groups.
The primary dependent variable is escape failure during avoidance training. 2-way analysis of variance (ANOVA) is used to assess overall treatment effect, with Dunn's post hoc analysis used to compare the vehicle-treated group with the drug-treated groups. The noinduction group is used to gauge whether learned helplessness is established, by comparison to the vehicle treated group.
Other assays that may be used to measure for example affinity of compounds of the present invention for 5HTIB and 5HTID receptors are described in J. Med. Chem 41:1218- 1235, 1228 (1998) and J. Med. Chem 42:4981-5001, (1999) and incorporated by reference herein. These assays may be used with some modifications: Frozen membrane preparations of a stably transfected chinese hamster ovary (CHO) cell line expressing 5-HT1B receptors and 5-HT1D receptors are thawed rapidly, briefly vortexed, and diluted in assay buffer (AB) containing 50 mM Tris-HC1, 4 mM MgClz, 4mM CaCl 2 1 mM EDTA, and adjusted to pH 7.4 with NaOH. Final protein concentrations are 0.185 mg/ml for 5-HTIB, and 0.4 mg/ml for HTID membranes. Test compounds are evaluated in competition assays using 3 H]-GR125743 (Amersham). The ligand concentration in both assays was 0.27nM. Kd for 3 H]-GR125743 may vary from 0.15 nM to 0.25 nM. The 5-HTIB and 5-HTID assays are performed simultaneously on one 96-well assay plate, one drug/compound per plate. Ten serial dilutions (1 uM to 4 pM, final concentration) of compound are prepared in DMSO from 10 mM stock solutions. Incubation mixtures are prepared in quadruplicate in 96-deep well assay plates (Matrix 1 ml). Final assay volumes per well are 10 pl compound/nonspecific; 100 pl membranes; 100 gl [3H]-GR125743; and 790 gl AB. Specific binding is defined by using uM Methiothepine. The assay plates are shaken for 5 min., and then incubated for an additional 55 min. Then the assay plates are filtered through Beckman GF/B filters (soaked 2 hrs. in PEI) using a Packard Filtermate 196. Filters are washed 2x with 1 ml ice-cold wash WO 02/055014 PCT/SE02/00070 -27buffer (5 mM Tris-HCI pH7.4 with NaOH). After the filters are dried, 35 pl of is added to each well. The plates are then counted on a Packard TopCount to determine CPM's per well. Ki values are determined for each test compound utilizing the graphic and analytical software package, GraphPad Prism. Compounds are then ranked in order of potency, and selectivity for 5-HTsB over 5-HT1D receptors.
A method that may be used to determine a compound's affinity for 5-HTIB and 5HT1D receptors is a guinea pig cortical test. This assay is described in detail by Roberts, et al, Br. J.
Pharmacol., 1996, 117, 384-388, which is incorporated by reference herein. The test is carried out as follows: Guinea pigs are decapitated and the cortici is dissected out, weighed and homogenized in 50 mM Tris-HC1, pH 7.7 with an Ultra-Turrax followed by centrifugation for 10 min at 48000 x g and 5 0 C. The pellet is resuspended and recentrifuged.
The final pellet is suspended in 0.32 M sucrose buffer to a concentration of 0.5g original wet weight per mL and stored frozen at -70 0 C. The radioligand binding assay is carried out as follows: 3 H]GR125743 saturation studies are tested in duplicate with 3-4 mg w.w. per tube in 5 mL buffer (50 mM Tris, 4 mM CaC12, 4 mM MgC12 and 1 mM EDTA at pH and a concentration range of 0.012 2 nM (10-12 concentrations) for the radioligand. Non-specific binding is determined in the presence of 10 mM methiothepin. In competition experiments 4- 8 mg w.w. per tube and a radioligand concentration of 0.2 nM are used with 10 -12 concentrations of the competing drug. The assays are run for 2-4 hours at 30 0 C and terminated by rapid filtration through Whatman GF/B filters (pretreated with 0.1% polyethyleneimine) using a Brandel cell harvester. Bovine serum albumin is added to the washing buffer to reduce non-specific binding. Data from the experiments may be analyzed using the iterative non-linear curve-fitting program LIGAND. The Kd values obtained from the saturation studies are used in the calculation of the Ki values by the LIGAND program. The Kd value of 3 H]GR125743 may result in a measurement of 46 4 pM and the Bmax in a measurement of 4.9 0.2 pmol/g w.w.
A GTPyS binding assay may used to determine whether a compound is a 5HTIB or 5HT1D agonist or antagonist. One assay available measures agonist stimulated GTP binding for example as set forth by Lazareno, S. (1999) Methods in Molecular Biology 106: 231-245.
Membrane preparations of a stably transfected CHO cell line expressing human receptors are purchased for example from Unisyn, Hopkinton, MA. Frozen membranes are thawed, briefly sonicated, and diluted to 167gg/ml protein in assay buffer containing 20 mM HEPES, 100 mM NaC1, ImM MgCL 2 and 1M GDP, pH adjusted to 7.4 with NaOH.
WO 02/055014 PCT/SE02/00070 -28- Diluted membranes are briefly homogenized with a Polytron and allowed to equilibrate at room temperature for at least 15 minutes before use. Serial dilutions (10 [LM to 1 pM, final concentration) of test compounds are prepared in buffer with and without 100 nM 5-HT (final concentration) from 10 mM DMSO stock solutions. Incubation mixtures are prepared in quadruplicate in 96-well, deep-well plates and consisted of 180 ptL of membranes (30 pLg protein) and 40 gL of compound with or without 5-HT. After an incubation period of minutes at room temperature, 20 giL of 3 SS]GTPyS (NEN; 100 pM final concentration) is added to begin the assay. Mixtures are shaken for 2 minutes and incubated at room temperature for an additional 28 minutes. The reaction is stopped by rapid filtration through Beckman GF/B glass fiber filters using a 96-well Packard cell harvester. Filters are washed four times with 1 mL ice-cold water. The filter plates are nominally dried and 30 gL of scintillation cocktail (MicroScint 40, Packard) is added to each well. CPMs for each well is determined using a TopCount Scintillation Counter (Packard). Maximum stimulation of 3 S]GTPyS binding is defined in the presence of 100nM 5-HT. Basal 35 S]GTPyS binding is defined in buffer alone. IC50 values are defined as the concentration of compound at which of the 100nM 5-HT response [was] obtained. Maximal intrinsic activity (IA) of a compound is defined as the percent maximal 5-HT-induced stimulation by 10 pM compound in the absence of 5-HT. As an inter-assay standard, a concentration response curve of (1 pM to IpM final) in the absence of compounds was included in each assay and an EC 5 0 was determined.
Preferred compounds of the present invention include, but are not limited to, the following compositions listed in Table 1 on the following pages.
WO 02/055014 PCT/SE02/00070 -29 Table 1: Compounds.
tire I Name 8-(4-methyl- 1-piperazinyl)-N-[4-(4morpholinyl)phenyl]-4-oxo-4Hchromene-2-carboxamide 2-{l1-[4-(2-Methoxy-phenyl)piperazin- 1-yl] -methanoyl methyl-piperazin-1 -yl)-chromen-4one 1-[4-(1-Acetyl-2,3-dihydro-1Hindol-6-yl)-piperazin- 1-yl]methanoyl}-8-(4-methyl-piperazin- I -yl)-chromen-4-one 2-Chloro-5-(4-{ 1-[8-(4-methylpiperazin- 1-yl)-4-oxo-4H-chromen- 2-yl]-methanoyl -piperazin- Il-yl)b~nzonitrile 2- {11-[4-(4-Methoxy-phenyl)piperazin- 1 -yl]-methanoyl metliyl-piperazin-1 -yl)-chromen-4one 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 411-cbromene-2-carboxylic acid furan-2-yl-l1H-pyrazol-3-yl)-amide WO 02/055014 WO 02/55014PCT/SE02/00070 8-(4-Methyl-piperazin- 1-yl)-4-oxo- 4H-chromene-2-carboxylic acid (4imidazol- 1-yl-phenyl)-amide 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4L-cromene-2-carboxylic acid (4- [1 ,2,3]thiadiazol-5-yl-plienyl)amide 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4H-chromene-2-carboxylic acid 4- [1 ,2,3]thiadiazol-5-yl-benzylamide 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4H-chromene-2-carboxylic acid [4- (4-acetyl-piperazin- 1 -yl)-phenyl]amide' 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4H-chromene-2-carboxylic acid (4-niethanesulfonyl-piperazin- l-yl)phenylil-amide 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4H-ch~romene-2-carboxylic acid (2methoxy-4-morpholin-4-yl-phenyl)amide WO 02/055014 WO 02/55014PCT/SE02/00070 -31- -Structure* Namfe o0-4Mty-ieazn y)4oo 4H-chromene-2-carboxylic acid (3- N CI chloro-4-morpholin-4-yl-phenyl)o amnide 0 :0 N o 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4H-chromene-2-carboxylic acid (4thiomorpliolin-4-yl-phenyl)-amide
N
o 8-(4-Methyl-piperazin- 1 -yl)-4-oxool N 0,(2,5-diethoxy-4-motpholin-4-ylo phenyl)-amide 0 0
N
0 8-(4-Methyl-piparazin- I -yl)-4-oxo- 4H-chromene-2-carboxylic acid (4- N Cyanomethyl-pheniyl)-amide *0 :A 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 411-cbromene-2-carboxylic acid N 0 0N 0 8-(4-Methyl-piperazin- 1 -yl).4-oxo- 4H-chromene-2-carboxylic acid [4- N (1 -morpholin-4-yl-methanoyl)- 0 0 phenyl]-amide WO 02/055014 WO 02/55014PCT/SE02/00070 -32- Structure Namo 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4E-chromene-2-carboxylic acid [4- N (2,6-dimethyl-morpholin-4-yl)- Iphenyl]-amide 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-.
4H-chromene-2-carboxylic acid [4- (4-fluoro-phenoxy)-phenyl]-amide 8-(4-Methyl-piperazin- 1l-yl)-2-(6morpholin-4-yl-benzooxazol-2-yl)chromen-4-one 8-(4-Methyl-piperazin- 1-yl)-4-oxo- OH 4H-chromene.-2-carboxylic acid (2- N hydroxy-4-morpholin-4-yl-phenyl)- -Irl~l .amide 8-(4-Methyl-piperazin- I -yl)-4-oxo- 4H-chromene-2-carboxylic acid NI ethoxy-benzothiazol-2-yl)-amide 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- 4H-chromene-2-carboxylic acid (4bromno-phenyl)-amide WO 02/055014 WO 02/55014PCT/SE02/00070 -33 Example SrtreNO,-= 0 8-(4-Methylpiperazin- 1-yl)-4-oxo- I I 4H-chromene-2-carboxylic acid N methyl-(4-morpholin-4-yl- N phenyl)arnide
N)
26 08 -(4-Methyl-pip erazin- 1 -yI)-4-oxo r o 4H-chromene-2-carboxylic acid (3- N N" morpholin-4-yl-phenyl)-amide N 0 27 0 8- (4-Methyl-piperazin- 1-yl)-4-oxo- I '-...4f1-chromene-2-carboxylic acid (3- N CN cyano-4-morpholin-4-yl-phenyl)q amnide N 0
N
28 0 8-(4-Methyl-piperazin- 1-yl)-4-oxo- 4f--chromene-2-carboxylic acid (3- N F fluoro-4-morpholin-4-yl-phenyl)o amide N) 0 29 0 {l1-[8-(4-Methy1-piperazin- 1yI)-4-oxo-4H-chromnen-2-yl]- N, methanoyl}-amino)-phenyll- 0 'Npiperazine- 1-carboxylic acid tert- N 0 C) 0N butyl ester 0 8-(4-Methyl-piperazin- 1 -yl)-4-oxo- I 4H-chromene-2-carboxylic acid (4- N piperazin- 1 -yl-phenyl)-amide (ND 0 0 N>
NH
WO 02/055014 WO 02/55014PCT/SE02/00070 -34 6-Methoxy-8-(4-methyl-piperazin- I.-yl)-4-oxo-4H-chromene-2carboxylic acid (4-morpholin-4-ylphenyl)-amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-41-chromene-2carboxylic acid methanesulfonyl-piperazin-1 -yl)phenyll-amide 6-Methoxy-8-(4-Methyl-piperazin- I -yl)-4-oxo-4H-chromene-2carboxylic acid (3-chloro-4morpholin-4-yl-phenyl)-amnide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-41{-chromene-2carboxylic acid (3-fluoro-4morpholin-4-yl-phenyl)-amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid (2-methoxy-4morpholin-4-yl-phenyl)-amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid (4-thiomorpholin-4yI-phenyl)-amide WO 02/055014 WO 02/55014PCT/SE02/00070 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-cbromene-2carboxylic acid [4.-(2,6-dimethylmorpholin-4-yl)-phenyl]-amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid (3-morpholin-4-ylphenyl)-amide 6-Methoxy-8-(4-methyl-piperazin.
1 -yl)-4-oxo-4 'H-cliromene-2.
carboxylic acid {4-[4-(2-hydroxyethyl)-piperazin- 1-yl]-phenyl} amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid [4-(1-morpholin-4yl-methanoyl)-'phenyl]-amide 6-Methoxy-8-(4-methyl--piperazin- I -yl)-4-oxo-4H-chromene-2carboxylic acid (3-cyano-4morpholin-4-y1-phenyl)-amide 4.{4-({l1-[6-Methoxy-8-(4-methylpiperazin- 1-yl)-4-oxo-4H-chromen- 2-yl]-methanoyl}-amino)-phenyl]piperazine-l1-carboxylic acid tertbutyl ester WO 02/055014 WO 02/55014PCT/SE02/00070 -36 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid (4-piperazin- l -ylphenyl)-amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid [4-(4-propionylpiperazin- 1 -yl)-phenyl]-amide 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid [4-(4-ethane sulfonyl-piperazin- 1 -yl)-phenyl]amide 6-Methoxy-8-(4.-methyl-piperazin- 1 -yl)-4-oxo-4H-cbromene-2carboxylic acid [4-(4-dimnethyl sulfamoyl-piperazin- 1 -yl)-phenyl]amide {l1-[6-Methoxy-8-(4-inethylpiperazin- 1 -yl)-4-oxo-4H-chromen- 2-yl]-methanoyl} -amino)-phenyl] piperazine- 1 -carboxylic acid dimethylamide {l1-[6-Methoxy-8-(4-methylpiperazin- 1-yl)-4-oxo-4H-cbromen- 2-yl]-methanoyl} -amino)--phenyl] piperazine-l1-carboxylic acid ethylamide WO 02/055014 WO 02/55014PCT/SE02/00070 -37 Examole Structure Name 49 0 I-[6-Methoxy-8-(4-methyl- I 0 piperazin- 1-yl)-4-oxo-4H-chromen- N N. 2-yl]-methanoyl }-amino)-phenyl]- N 0o piperazine- 1-c arboxylic acid C) 0N-" cyclohexylarnide
NC)-I
0 4-[4-({11-[6-Methoxy-8-(4-methylpiperazin- 1-yl)-4-oxo-4H-cbromen- N 2-yl]-methanoyl}-amino)-phenyl]- 0 N.piperazine- 1-carboxylic acid 0N- cyclopentylamide 0 51 0 6-Methoxy-8-(4-methyl-piperazin- N. 1 -yl)-4-oxo-4H-cbromene-2- 1 1 N Iacarboxylic acid 14-[4-(l -pyrrolidino 1 -yl-methanoyl)-piperazin-1 -yl]-
CN
0 0 -~Nphenvl-amide 52 0 6-Methoxy-8-(4-methyl-piperazin- A 1 -yl)-4-oxo-4H-chromene-2- I N. carboxylic acid {4-[4-(propane-2- 0 o sulfonyl)-piperazin-1 -yl]-phenyl (N N amide 53 0 6-Methoxy-8-(4-methyl-piperazin- N.0 1 -yl)-4-oxo-4H-chromene-2- N carboxylic acid {4-[4-(2-inethylo N prop anoyl) -p iperazin- 1 yl] -phenyl) 0 N amide 1 .0 54 0 6-Methoxy-8-(4-methyl-piperazin- 0 1 -yl)-4-oxo-411-chromene-2- N N. carboxylic acid 1-morpholin- 0 4-yl-methanoyl)-piperazin- l-yl]- N 0 Nphenyl}-amide 0 WO 02/055014 WO 02/55014PCT/SE02/00070 -38- 6-Fluoro-g-(4-methyl-piperazin- 1yl)-4-oxo-4H-chromene-2carboxylic acid (4-morpholin-4-ylphenyl)-amide 6-Fluoro-8-(4-methyl-piperazin- 1yl)-4-oxo-411-chromene-2carboxylic acid methanesulfonlyl-piperazin- Il-yl)phenyl]-amide 6-Fluoro-8-(4-niethyl-piperazin-1 yl)-4-oxo-4H-chromene-2carboxylic acid [4-(4-acetylpiperazin- 1 -yl)-phenyl]-amide 6-Fluoro-8-(4-mnethyl-piperazin- 1 yl)-4.-oxo-4H-chromene-2carboxylic acid (3-chloro-4morpholin-4-yl-phenyl)-amide 6-Fluoro-8-(4-methyl-piperazin- 1 yl)-4-oxo-4H-cbromene-2carboxylic acid (3-fluoro-4morpholin-4-yl-phenyl)-amide 6-Fluoro-8-(4-methyl-piperazin- 1 yl)-4-oxo-4H-eromene-2carboxylic acid (3-cyano-4morpholin-4-yl-phenyl)-amfide i WO 02/055014 WO 02/55014PCT/SE02/00070 -39
I
rNamfe 6-Fluoro-8-(4-methyl-piperazin- 1 yl)-4-oxo-4H-chromene-2carboxylic acid [4-(1-morpholin-4yl-mnethanoyl)-phenyl]-amide 6-Methyl-8-(4-methyl-piperazin- 1yl)-4-oxo-4H-cbromcne-2carboxylic acid (4-morpholin-4-ylphenyl)-amide 6-Methyl-8-(4-methyl-piperazin- 1 yl)-4-oxo-41{-chromene-2carboxylic acid -morpholin-4yl-methanoyl)-phenyl]-amide 6-Methy1-8-(4-methy-piperazin- 1yl)-4-oxo-411-chromene-2carboxylic acid (3-fluoro-4morpholin-4-yl-phenyl)-amide 6-Cloro-8-(4-methyl-piperazin- 1yl)-4-oxo-4ET-chromene-2carboxylic acid (4-morpholin-4-ylphenyl)-amide 5-Methyl-g-(4-methyl-piperazin- 1yl)-4-oxo-4H-chromene-2carboxylic acid (4-morpholin-4-ylphenyl)-amide WO 02/055014 WO 02/55014PCT/SE02/00070 Example Structure Narne 67 05-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2- N carboxylic acid (4-morpholin-4-yl- Q phenyl)-amide (ND 0 0 N N carboxylic acid f{4-[4-(3-hydroxy- 0 propanoyl)-piperazin- 1 -yl]-phenyl} 0N N)O amnide 69 0 -[6-Fluoro-8-(4-methyl- F NNpiperazin- 1 -yl)-4-oxo-4H-chromen- 2-yl]-methanoyl }-amino)-phenyl]- 1% 1 piperazine- 1 -carboxylic acid tert- 0N butyl ester 0 1-[6-Fluoro-8-(4-methlyl- F 1ieazn -yl)-4-oxo-4H- NN chromene-2-carboxylic acid (4- 0 k i piperazin-1I -yl-phenyl)-amide N*
NH
71 0 6-Fluoro-8-(4-methyl-piperazin-1 F yl)-4-oxo-4H-chromene-2- IN N carboxylic acid [4-(4-ethane q O N% sulfonyl-piperazin- 1 -yl)-phenyl] N 0-a amide N 0 0 72 06-Fluoro-8-(4-metliyl-piperazin-1 F yl)-4-oxo-411-chromene-2- N carboxylic acid [4-(4-propionyl- O N piperazin-l -yl)-phenyl]-amide CN) 0N 1 0 WO 02/055014 WO 02/55014PCT/SE02/00070 -41 N,-ine 6-Fluoro-S-(4-methyl-piperazin- 1 yl)-4-oxo-4H-chromene-2carboxylic acid {4-[4-(3-hydroxypropanoyl)-piperazin- 1-yl]-plienyl} amide 4-Methyl-piperazin- 1 -y1)-z1oxo-411-chromen-2-yl]-4morpholin-4-yl-benzamide 8-(4-Methyl-piperazin- Il-yl)chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (+)-8-(4-Methyl-piperazin- l-yl)chroman-2-carbDXylic acid (4morpholin-4-yl-phenyl)-amide (-)-8-(4-Methyl-piperazin- l-yl)cbroman-2-carboxylic acid (4rnotpholin-4-yl-phenyl)-arnide racemic-8-.(4-methyl-piperazin-1 yl)-4-oxo-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)amide WO 02/055014 WO 02/55014PCT/SE02/00070 -42 Structure Name 8-(4-Methyl-piperazin- I -yl)-4-oxochroman-2.-carboxylic acid (4morpholin-4-yl-phenyl)-amide (faster running isomer) 8-(4-Methyl-piperazin- 1 -yl)-4-oxochroman-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide (slower running isomer).
4-[4-Q 1 -[6-Fluoro- 8-(4-methylpiperazin- 1-yl)-4-oxo-4H-chromen- 2-yl]-methanoyl}-amino)-phenyl]piperazine- 1-carboxylic acid ethylamide 6-Methoxy-8-(4-methyl- [1 ,4]diazepan-1 -yl)-4-oxo-4Hchromene-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide 6-Ethoxy-8-(4-methyl-piperazin- 1 yl)-4-oxo-4H-chromene-2carboxylic acid (4-morpholin-4-ylphenyl)-amide 6-Ethoxy-8-(4-methyl-piperazin- 1 yl)-4-oxo-4H-chromene-2carboxylic acid [4-(4-propionylpiperazin- 1 -yl)-phenyl] -amide WO 02/055014 WO 02/55014PCT/SE02/00070 -43 Name 6-Methoxy-4-oxo-8-piperazin- 1 -yl- 4H-chromene-2-carboxylic acid (4morpholin-4-yl-plienyl)-amnide 6-Hydroxy-8-.(4-mcthyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid (4-morpholin-4-ylphenyl)-amide 6-Methoxy-8-(4-methyl- [1,41 diazepan- 1 -yl)-4-oxo- 1,4dihydro-quinoline-2-carboxylic acid (4-moipholin-4-yl-phenyl)-amide 6-Methoxy-8-(4-methyl-piperazin- H 1 -yl)-4-oxo- 1,4-dihydro-quinoline- N 2-carboxylic acid (4-morpholin-4yl-phenyl)-amide 6-Methoxy-8-(4-methyl-'piperazin- 1 -yl)-4-oxo- 1,4-dihydro-quinoline- 2-carboxylic acid [4-(4-propionylpiperazin- 1-yl)-phenyl]-amide 6-Fluoro-8-(4-methyl-piperazin- 1yl)-4-oxo- 1,4-dihyclro-quinoline-2carboxylic acid (4-morpholin-4-ylphenyl)-amide WO 02/055014 WO 02/55014PCT/SE02/00070 -44 6-Fluoro-8-(4-methyl-piperazin- I1yl)-4-oxo-1 ,4-dihydro-quinoline-2l Na carboxylic acid [4-(4-propionylci 'Npiperazin-1 -yl)-phenyl]-amide
N
0 0 8-[(2-Dimethylamino-ethyl)methyl-amino] -6-methoxy-4-oxo- N 1 ,4-dihydro-quinoline-2-carboxylic N acid (4-morpholin-4-yl-phenyl)- N amide o 8-[(3-Dimethylamino-propyl)- H methyl-amino]-6-methoxy-4-oxo- -CN ,4-dihydro-quinoline-2-carboxylic N acid (4-morpholin-4-yl-phenyl)- I0 o 8-((3R)-(+)-3-DimethylaminO7 H pyrrolidin -1-yl)-6-methoxy-4-oxo- I 1 ,4-dihydro-quinoline-2-carboxylic N N acid (4-morpholin-4-yl-phenyl)-
H
0 N) amide 0 8-((3S)-(-)-3-Dimetliylarnino- H pyrrolidin -1 -yl)-6-methoxy-4-oxo- N .1 ,4-dihydro-quinoline-2-carboxylic N N acid (4-mnorpholin-4-yl-phenyl)- H 0 amide o 6-Methoxy-8- [methyl-( 1-methyl- H pyrrolidin-3-yl)-amino]-4-oxo- 1,4- I N dihydro-quinoline-2-carboxylic acid H. Nn (4-morpholin-4-yl-phenyl)-amide WO 02/055014 WO 02/55014PCT/SE02/00070 Name 8-[Ethyl-(1 -ethyl-pyrrolidin-3-yl)amino]-6-methoxy-4-oxo- 1,4dihydro-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide N 4-dimethylamino-6-methoxy-8-(4- H methyl-piperazin-1 -yl)-quinoline-2- H carboxylic acid (4-morpholin-4-yl- I N phenyl)-amide N I6-methoxy-4-methylarnino-8-(4methyl-piperazin-1 -yl)-quinoline-2- H carboxylic acid (4-morpholin-4-yl- N phenyl)-amide I6-fluoro-4-methoxy-8-(4-methylpiperazin- 1-yl)-quinoline-2carboxylic acid (z-morpholin-4-ylphenyl)-amide 6-Fluoro-4-oxo-8-piperazin- 1-yl- 4H-chromene-2-carboxylic acid (4morpholin-4-yl-plienyl)-amide Also provided herein'are the pharmaceutically acceptable salts of the compounds set forth in Table 1.
WO 02/055014 PCT/SE02/00070 -46- The following reference examples illustrate the making of intermediates in the synthesis of the compounds of the present invention, and are not intend to limit the invention in any manner.
Reference Example 1 Preparation of Reference Example 1: 8-(4-Methyl-piperazin-l-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride.
Reference Example la: (E,Z)-2-(2-Bromo-phenoxy)-but-2-enedioic acid diethyl ester.
Diethyl acetylenedicarboxylate (20 ml, 0.162 mol) was added to 2-bromophenol (28 g, 0.162 mol), in anhydrous 2-propanol (60 ml) followed by the addition of a catalytic amount of tetrabutylammonium fluoride (0.5 ml, 1.0 M in THF). The solution was stirred at room temperature four hours and was then heated to reflux for one hour. The mixture was cooled to room temperature, then concentrated under vacuum to an oil (51 g 91%).
Reference Example Ib: (E,Z)-2-(2-Bromo-phenoxy)-but-2-enedioic acid.
(E,Z)-2-(2-Bromo-phenoxy)-but-2-enedioic acid diethyl ester (51 g, 148 mmol) as prepared in Reference Example la was suspended in ethanol (95 ml) and a solution of sodium hydroxide 12.9 g, 0.323 mol) in water (95 ml) was added. The solution was refluxed for 1 h to give a clear orange solution. The mixture was cooled to room temperature and acidified with 6 M HC1 (50 ml). The mixture was then concentrated under vacuum and the residue azeotroped (4x) with ethanol. The solid was filtered, washed with water and dried to give (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acid as a light orange solid (24.3 g, 88 yield). This crude product was used without further purification.
Reference Example le: Ethyl-8-Bromo-4-oxo-4H-chromene-2-carboxylate.
Sulfuric acid (95mL) was added to crude (E,Z)-2-(2-Bromo-phenoxy)-but-2-enedioic acid as prepared in Reference Example lb. After heating the mixture with a heat gun for min an orange milky solution was obtained. This solution was slowly added to refluxing absolute ethanol (500 mL). After the addition, the reaction was refluxed for 30 min.then allowed to cool. Crystals started to form after 20 min and the reaction was put in the refrigerator overnight. The solid was filtered, washed with cold ethanol/ water 9:1 and dried to give ethyl 8-bromo-4-oxo-4H-chromene-2-carboxylate as an off-white solid (11.7 g, 24 yield, mp 124-126 OC).
WO 02/055014 PCT/SE02/00070 -47- Reference Example ld: Ethyl-8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromenec-2carboxylic acid.
Ethyl 8-bromo-4-oxo-4H-chromene-2-carboxylate as prepared in Reference Example Ic (Davies, Stephen et al., J. Chem. Soc. Perkin Trans I p 2597, 1987) (3.0 g, 10.1 mmol) was azeotroped with anhydrous toluene then the white solid was dissolved in 100 mL anhydrous toluene and transferred to the reaction vessel. The.mixture was subjected to vacuum argon (x2) and the following were added in order (positive argon pressure): N-methylpiperazine (1.3 ml, 11.1 mmol), 2,2'-bis (diphenylphosphino)-1,1l'-binaphthyl (0.75 g, 1.2 mmol,), tris(dibenzylideneacetone) dipalladium (0.48 g, 0.5 mmol) then cesium carbonate (4.6 g, 14.1 mmol).The mixture was again subjected to vacuum argon and was heated at 80 °C overnight.
The cooled reaction mixture was filtered through diatomaceous earth and the toluene solution was applied directly to a 600 ml filter funnel (silica 230 400 mesh ASTM packed in ethyl acetate) and then washed with ethyl acetate (2 The product was eluted with 5-8 methanol chloroform and the desired was collected to give 2.5 g of a slightly impure orange yellow solid (mp 120-123 The impure product was chromatographed on a Waters Delta Prep 4000 using 1 PrepPak cartridge (Porasil 37-55pm 125A) eluting with 3-5 methanol/ chloroform. The product was collected and dried to give ethyl 8-(4-methyl-1-piperazinyl)-4oxo-4H-chromene-2-carboxylate as a yellow solid (2.25 g, 70 yield mp 124-125 GC/MS (EI, m/z 316.
Reference Example e: 8-(4-methyl-1 -piperazinyl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride.
Ethyl 8-(4-methyl- 1-piperazinyl)-4-oxo-4H-chromene-2-carboxylate as prepared in Reference Example Id (1.01 g. 3.19 mmol) was suspended in 6 M HCI (60 ml) and to reflux for 1.5 h (after 20 min a clear solution was obtained).
The reaction was allowed to cool. The solution was concentrated in vacuo and anhydrous toluene was added (x3) and the solution was again concentrated in vacuo to give 8-(4-methyl- 1-piperazinyl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride as a yellow powder (1.02 g, quantitative yield). LC/MS m /z 289.
WO 02/055014 PCT/SE02/00070 -48- Reference Example 2
H
3 0
OH
00O
H
N 0
HCI
Preparation of 6-Methoxy-8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride.
Reference Example 2a: Diethyl (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate.
Ethyl acetylenedicarboxylate (17.8 ml, 0.145 mol) was added to 2-bromo-4methoxyphenol (Synlett p1241, 1997) (27.3 g, 0.134 mol), in anhydrous 2-propanol (55 ml) followed by the addition of a catalytic amount of tetrabutylammonium fluoride (0.4 ml, 1.0 M in THF). The solution was stirred at room temperature overnight and was then heated to reflux for 30 min. Upon cooling a precipitate formed. The solution was cooled and filtered to give diethyl (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate as a yellow solid (29.9 g, 62 yield). Note: the solid contains 10 of diethyl (2E)-2-(2-bromo-4-methoxyphenoxy)-2butenedioate. GC/MS (EI, m/z 344 and 346.
Reference Example 2b: (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acid.
Diethyl (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioate (29.9 g, 86.6 mmol) as prepared in Reference Example 2a was suspended in ethanol (55 ml) and a solution of sodium hydroxide 7.0 g, 0.175 mol) in water (55 ml) was added. The solutionwas refluxed for 1 h to give a clear orange solution. Most of the ethanol was removed in vacuo then 6 M HC1 ml) was added. The solid was filtered, washed with water and dried to give (2Z)-2-(2-bromo- 4-methoxyphenoxy)-2-butenedioic acid as a light orange solid (24.3 g, 88 yield).
Reference Example 2c: Ethyl-6-methoxy-8-bromo-4-oxo-4H-chromene-2-carboxylate.
Sulfuric acid (50ml) was added to (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acid (24.3g, 86.6 mmol; as prepared in Reference Example 2b above). After heating the mixture with a heat gun for 5-10 min a clear deep brown solution was obtained. This solution was slowly added to refluxing absolute ethanol (250 ml). After the addition the reaction was refluxed for 30 min then allowed to cool. Crystals started to form after 20 min and the reaction was put in the refrigerator overnight. The solid was filtered, washed with cold ethanol/ water WO 02/055014 PCT/SE02/00070 -49- 9:1 and dried to give ethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylate as an offwhite solid (12.3 g, 50 yield, mp 159-161 Reference Example 2d: Ethyl-6-methoxy-8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene- 2-carboxylate.
Ethyl 8-bromo-4-oxo-4H-chromene-2-carboxylate (9.2 g, 28.1 mmol), as prepared in Example 2c above, was azeotroped with anhydrous toluene then the white solid was dissolved in 300 ml anhydrous toluene in a 500 mL single-neck round bottom flask.. The mixture was degassed by alternating argon sparge and vacuum and the following were added in order: N-methylpiperazine (4.0 ml, 35.1 mmol), 2,2'-bis (diphenylphosphino)-1, '-binaphthyl (1.05 g, 1.69 mmol,), tris(dibenzylideneacetone) dipalladium (0.50 g, 0.56 mmol) then cesium carbonate (12.8 g, 39.3 mmol).The mixture was again degassed via alternating argon sparge and vacuum and was heated at 80 OC for 17 h. Additional tris(dibenzylideneacetone) dipalladium (0.10 g, 0.11 mmol) and 2,2'-bis (diphenylphosphino)-1, '-binaphthyl (0.20 g, 0.32 mmol,) was added and the reaction was stirred at 80 OC for another 55 h at which time the conversion was essentially complete.
The cooled reaction mixture was diluted with tetrahydrofuran (250 mL), filtered and concentrated under vacuum. The residue was purified by chromatography on a silica column eluted with 2-5 methanol chloroform and the desired fractions were collected and concentrated under vacuum and the residue triturated with methylene chloride to. give 7.4 g of a yellow powder.
Reference Example 2e: 6-Methoxy-8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene-2carboxylic acid.
Ethyl-6-methoxy-8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene -2-carboxylate (1.0 g.
2.89 mmol), as prepared in Reference Example 2d above, was suspended in 6 M HC1 (60 ml) and methanol (10 mL) and warmed to reflux for 3.0 h. The reaction was allowed to cool. The solution was concentrated in vacuo and anhydrous toluene was added (x3) and the solution was again concentrated in vacuo. The residue was dried under vacuum (17 h) to yield 6methoxy-8-(4-methyl-1 -piperazinyl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride as a yellow powder (1.0 g, quantitative yield).
Reference Example 3 WO 02/055014 PCT/SE02/00070 0
F
I OH 0 6-Fluoro-8-(4-methyl-piperazin-1-yI)-4-oxo-411-chromene-2-carboxylic acid hydrochloride.
Reference Example 3a: Diethyl (EZ)-2-(2-bromo-4-fluorophenoxy)-2-butenedioate.
This compound was synthesized from 2-bromo-4-fluorophenol and diethylacetylenedicarboxylate, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example la above.
Reference Example 3b: (EZ)-2-(2-Bromo-4-fluorophenoxy)-2-butenedioic acid.
This compound was synthesized from diethyl (EZ)-2-(2-bromo-4-fluorophenoxy)-2butenedioate, as prepared in Reference Example"3a above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example lb above.
Reference Examiple 3c: Ethyl-6-fluoro-8-bromo-4-oxo-4H-chromene-2-carboxylate.
This compound was synthesized from (EZ)-2-(2-bromo-4-fluorophenoxy)-2butenedioic acid, as prepared in Reference Example 3b above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example 1 c above.
Reference Example 3d: Ethyl-6-ffuoro-8S-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2carboxylate.
This compound was synthesized from ethyl-6-fluoro-8-bromo-4-oxo-4H-chromene-2carboxylate, as prepared in Reference Example 3c above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example I d above.
Reference Example 3e: 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-cbromene-2carboxylic acid hydrochloride.
This compound was synthesized starting from ethyl-6-methoxy-8-(4-Methylpiperazin.. 1 yl)-4-oxo-4H-chromene-2-carboxylate, as prepared in Example 3 d, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example I e above.
WO 02/055014 PCT/SE02/00070 -51 Reference Example 4 0
H
3
C
I OH
OH
0 N 0-
HCI
N
Preparation 6-Methyl-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride.
Reference Example 4a: Diethyl (E,Z)-2-(2-bromo-4-methylphenoxy)-2-butenedioate.
2-Bromo-4-methyl phenol (10 mL, 83mmol) was dissolved in diethyl ether (90 mL). To this was added dropwise triethyl amine (13.7 mL, 98mmol) followed by dimethyl acetylene dicarboxylate (11.2 mL, 91 mmol). The resulting mixture was stirred overnight at room temperature. The reaction was worked up by adding diethyl ether (200 mL) and tetrahydrofuran (50 mL) and washing the resulting mixture with IN HCI (200 mL), water (200 mL) and brine (100 mL). The organic phase was then dried (Na 2 SO04), filtered and concentrated to a red-brown oil which was used without further purification.
Reference 4b: (2E,Z)-2-(2-Bromo-4-fluorophenoxy)-2-butenedioic acid.
This compound was synthesized from diethyl (E,Z)-2-(2-bromo-4-methylphenoxy)-2butenedioate, as prepared in Reference Example 4a above, using the same synthetic procedures and the same stoichiometry as demonstrated in Example lb above.
Reference Example 4c: Ethyl-6-methyl-8-bromo-4-oxo-4H-chromene-2-carboxylate.
This compound was synthesized from (2Z)-2-(2-bromo-4-methylphenoxy)-2butenedioic acid, as prepared in Reference Example 4b above, and using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example Ic above.
Reference Example 4d: Ethyl-6-methyl-8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylate.
This compound was synthesized from ethyl-6-methyl-8-bromo-4-oxo-4H-chromene-2carboxylate, as prepared in Reference Example 4c above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example 1d above.
WO 02/055014 PCT/SE02/00070 52 Reference Example 4e: 6-Methyl-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid hydrochloride.
This compound was synthesized starting with ethyl-6-methyl-8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylate, as prepared in Reference Example 4d, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example le above.
Reference Example 0 C1
OH
0 N 0
HCI
Preparation of 6-Chloro-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride.
Reference Example 5a: Diethyl (E,Z)-2-(2-bromo-4-chlorophenoxy)-2-butenedioate.
This compound was prepared from 2-bromo-4-chloro phenol and dimethyl acetylenedicarboxylate by the same synthetic procedures and in the same stoichiometry as the preparation described in Reference Example 4a.
Reference Example 5b: (2E,Z)-2-(2-Bromo-4-chlorophenoxy)-2-butenedioic acid..
This compound was synthesized from diethyl (E,Z)-2-(2-bromo-4-chlorophenoxy)-2butenedioate, as prepared in Reference Example 5 a above, as using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example lb above.
Reference Example Sc: Ethyl-6-chloro-8-bromo-4-oxo-4H-chromene-2-carboxylate.
This compound was synthesized from (2E,Z)-2(2-bromo-4-chlorophenoxy)-2butenedioic acid, as prepared in Reference Example 5b above, using the same synthetic procedures and the same stoichiometry as.demonstrated in Example Ic above.
Reference Example 5d: Ethyl-6-chloro-8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2carboxylate.
WO 02/055014 PCT/SE02/00070 -53- This compound was synthesized from ethyl-6-chloro-8-bromo-4-oxo-4H-chromene-2carboxylate, as prepared in Reference Example 5c above, using the same synthetic procedures and the same stoichiometry as demonstrated in Example 1 d above.
Reference Example Se: 6-Chloro-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2carboxylic acid hydrochloride.
This compound was synthesized starting with ethyl-6-chloro-8-(4-methyl-piperazin- 1yl)-4-oxo-4H-chromene-2-carboxylate, prepared in Reference Example 5d above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example le above.
Reference Example 6
CH
3 0
OH
0 N O
HCI
N
Preparation of 5-Methyl-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride Reference Example 6a: Diethyl (E,Z)-2-(2-chloro-5-methylphenoxy)-2-butenedioate.
This compound was prepared from 2-chloro-5-methylphenol and dimethyl acetylenedicarboxylate by the same synthetic procedures and in the same stoichiometry as the preparation described in Reference Example la.
Reference Example 6b: (2E,Z)-2-(2-chloro-5-methylphenoxy)-2-butenedioic acid.
This compound was synthesized from diethyl (E,Z)-2-(2-chloro-5-methylphenoxy)-2butenedioate, as prepared in Reference Example 6a above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example lb above.
Reference Example 6c: Ethyl-5-methyl-8-chloro-4-oxo-4H-chromene-2-carboxylate.
This compound was synthesized from (2Z)-2-(2-chloro-5-methylphenoxy)-2butenedioic acid, as prepared in Reference example 6b, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example 1c above.
WO 02/055014 PCT/SE02/00070 -54- Reference Example 6d: Ethyl-5-methyl-8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene-2carboxylate.
Ethyl 5-methyl-8-chloro-4-oxo-4H-chromene-2-carboxylate (1.0 g, 3.6 mmol) as prepared in Reference Example 6c above, was azeotroped with anhydrous toluene then the white solid was dissolved in 100 ml anhydrous toluene in a 250 mL single-neck round bottom flask.. The mixture was degassed by alternating argon sparge and vacuum and the following were added in order: N-methylpiperazine (0.6 ml, 5.37 mmol), dicyclohexylphosphanyl-biphenyl-2-yl)-dimethyl-amine (JACS 1998, 120, p9722) (40 mg, 0.1 mmol,), tris(dibenzylideneacetone) dipalladium (66 mg, 0.072 mmol) then cesium carbonate (1.6 g, 5.37 mmol).The mixture was again degassed via alternating argon sparge and vacuum and was heated at 80 OC for 17 h. Additional tris(dibenzylideneacetone) dipalladium (66 mg, 0.072 mmol) and (2'-dicyclopentylphosphanyl-biphenyl-2-yl)dimethyl-amine (40 g, 0.1 mmol,) were added and the reaction was stirred at 80 °C for another four days at which time the conversion was still only about 50% complete by HPLC.
Tetrahydrofuran (100 mL) was added, and the combined mixture was filtered, concentrated under vacuum and purified by chromatography on silica eluted with 2.5% methanol in chloroform. The desired fractions were concentrated under vacuum to yield a yellow powder (250 mg 21%).
Reference Example 6e: 5-Methyl-8-(4-methyl-piperazin- -yl)-4-oxo-4H-chromene-2carboxylic acid hydrochloride.
This compound was synthesized starting with ethyl-5-methyl-8-(4-methyl-piperazin-1yl)-4-oxo-4H-chromene-2-carboxylate, as prepared in Reference Example 6d, and using the same synthetic procedures and the same stoichiometry as demonstrated in Example le above.
Reference Example 7 WO 02/055014 PCT/SE02/00070 Preparation of 5-Methoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-411-chromene-2-carboxylic acid hydrochloride.
Reference Example 7a: (E ,Z)-2-(2-Bromo-5-methoxyphenoxy)-2-butenedioate.
This compound was-prepared from, 2-bromo-5-methoxyphenol and dimethyl acetylenedicarboxylate by the same synthetic procedures and in the same stoichiometry as the preparation described in Reference Example 1 a.
Reference Example 7b: (E,Z)-2-(2-Bromo-5-methoxyphenoxy)-2-butenedioic acid.
This compound was synthesized from diethyl (E,Z)-2-(2-bromo-5-methoxyphenoxy)- 2-butenedioate, as prepared in Reference Example 7a, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example lb above.
Reference Example 7c: Ethyl-5-methoxy-8-bromo-4-oxo-4H-chromene-2-carboxylate.
This compound was synthesized from (E,Z)-2-(2-bromo-5-methoxyphenoxy)-2-butenedioic acid, as prepared in Reference Example 7b above, using the same synthetic procedures and the same stoichiometry as demonstrated in Reference Example lc above.
Reference Example 7d: Ethyl-5-methoxy-8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene- 2-carboxylate.
This compound was synthesized from ethyl-5-methoxy-8-bromo-4-oxo-4H-cbromene- 2-carboxylate, as prepared in Reference Example 7c above, using the same synthetic procedures and the same stoichiometry as demonstrated in. Reference Example I d above.
Reference Example 7e: 5-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2carboxylic acid hydrochloride.
This compound was prepared from ethyl-5-methoxy-8-(4-Methyl-piperazin- Il-yl)-4oxo-4H-chromene-2-carboxylate, as prepared in Reference Example 7d above, using the same method as the preparation in Ile.
Reference Example 8 0 CH 3
NNN
Preparation of 1-(6-Piperazin-1-yl-2,3-dihydro-indol-1-yl)-ethanone Reference Example 8a: 1 -[5-(4-Benzyl-piperazin- 1-yl)-2,3-dihydro-indol- 1-yl]-ethanone.
1 -acetyl-5-bromoindoline (3.0 g, 1 2.Snimol) was dissolved in toluene (60 mL). To this was added, sodium t-butoxide (1.68 g, 1 7.5mmol), N-benzylpiperazine (2.4 mL, WO 02/055014 PCT/SE02/00070 -56- 13.8mmol), S-BINAP (0.93 g, 1.5mmol) and Pd 2 (dba) 3 (0.46 g, 0.5mmol). The mixture was degassed via three cycles of vacuum and nitrogen sparge and then stirred at 95C until GC analysis confirmed that the reaction was complete (1 The mixture was diluted with ethyl acetate (150 mL), washed with water and extracted with 2N HCI (2 x 100 mL). The combined aqueous extract was basified with concentrated ammonium hydroxide and extracted with ethyl acetate (2 x 100 mL). The combined organic extract was dried (MgS04) and concentrated to yield a solid (2.7 g) which was purified by chromatography to yield a white solid (1.81 g, Mp= 150.5-152.8 0
C.
Reference Example 8b: 1-(6-Piperazin-1 -yl-2,3-dihydro-indol-1-yl)-ethanone.
1-[5-(4-Benzyl-piperazin-1-yl)-2,3-dihydro-indol-1-yl]-ethanone (0.37 g, 1.lmmol), as prepared in Reference Example 8a above, was dissolved in methanol (5 mL). Pd/C (90 mg, and ammonium formate (0.9 g, 14mmol) was added and the resulting mixture was heated to 65 0 C for two hours. The mixture was filtered and the filter cake washed with hot methanol. The combined filtrate was concentrated to yield the desired product (0.26 g, Reference Example 9
NC
CI-b- N NH Preparation of 2-chloro-5-piperazin-l-yl benzonitrile.
Reference Example 9a: 3-Cyano-4-chloroaniline.
(25 g, 137mmol) was dissolved in ethanol (275 mL).
Stannous chloride dihydrate (154.5 g, .685 M) was added and the mixture stirred at 70 0 C for min. The mixture was then cooled to room temperature and poured into crushed ice. The mixture was made basic with solid sodium hydroxide. This mixture was extracted with ethyl acetate (3 x 100 mL). The extracts were combined, washed with brine, dried (MgSO 4 concentrated and the residue dried under vacuum and rccrystallized from ethanol to yield light brown needles (10.6 g, 51%).
Reference Example 9b: 2-chloro-5-piperazin-l-yl benzonitrile.
3-Cyano-4-chloroaniline (10.1 g, 66mmol), as prepared in Reference Example 9a, was dissolved in n-butanol (300 mL) bis-(2-chloroethyl)amine hydrochloride (23.2 g, 130mmol) and potassium iodide (50 mg, catalytic) were added. The mixture was heated at reflux for three days, then cooled in a refrigerator overnight. A solid precipitate was collected by filtration, washed with cold n-butanol and dried. The crude product was distributed between WO 02/055014 PCT/SE02/00070 -57methylene chloride and 2N ammonium hydroxide. The organic layer was separated, dried (Na 2 S04) and concentrated to yield a light yellow solid (9.1 g, 59%) which gave a single peak by GC and TLC analysis.
Reference Example
H
2 N 11 H2 Preparation of 4-[1,2,3]thiadiazol-5-yl-phenylamine.
SnC12 H 2 0 (3.21 g, 5 eq) was added to a slurry of (5-(4-Nitrophenyl)- ,2,3thiadiazole (Lancaster Synthesis) (0.59 g, 2.8 mmol) in absolute EtOH (50 mL) and the reaction heated to 700 C for 2 h. The reaction was allowed to cool to room temperature and pour into saturated NaHCO 3 and ice. The product was extracted with EtOAc (2X) the solution dried (MgSO 4 and evaporated to dryness in vacuo to yield 0.47 g of a light yellow solid mp 126-1280 C.
Reference Example 11
H
2 N- N N
CH
3 Preparation of 1-[4-(4-Amino-phenyl)-piperazin-1-yl]-ethanone.
Reference Example lla: 4-(4-Nitrophenyl)-l-acetylpiperazine.
l-(4-Nitrophenyl)piperazine (2.5 g, 12.1 mmol) was dissolved in dichloromethane (100 ml). Triethylamine (2.0 ml, 14.5 mmol) was added and the reaction was cooled to 0 oC.
Acetic anhydride (1.25 ml, 13.3 mmol) was added dropwise and the reaction was stirred at 0 °C for 1 h. Saturated sodium bicarbonate was added and the reaction was extracted (x3) with dichloromethane, dried (MgSO 4 filtered and concentrated in vacuo to give 4-(4nitrophenyl)-l-acetylpiperazine as a yellow solid (3.01 g,).GC/MS (EI, m/z 249.
Reference Example 11b: 1-[4-(4-Amino-phenyl)-piperazin-l-yl]-ethanone.
4-(4-Nitrophenyl)-l-acetylpiperazine (3.0 g, 12.0 mmol), as prepared in Reference Example 1 la above, was mixed in methanol (100 ml) and 2 M ammonia in methanol (50 ml) and 10 palladium on carbon (300 mg) was added. The mixture was hydrogenated on a Paar apparatus psi) for 1.5 h.
The reaction was allowed to cool, the catalyst was filtered and the solution was concentrated in vacuo.. The crude solid was recrystallized from ethyl acetate to give 4-(4- WO 02/055014 PCT/SE02/00070 -58acetyl-l-piperazinyl)benzenamine as a light purple solid (1.86 g, 70 yield, mp 149.5-150.5 oC). GC/MS (EI, m/z 219 Reference Example 12 0
H
2 N N N-- VJ
CH
3 Preparation of 4-(4-methanesulfonyl-piperazin-1-yl)-phenylamine Reference 12a: 4-(4-Nitrophenyl)-l-methylsulfonylpiperazine.
1-(4-Nitrophenyl)piperazine (2.79 g, 13.5 mmol) was dissolved in dichloromethane (100 ml). Triethylamine (2.25 ml, 16.2 mmol) was added and the reaction was cooled to 0 0
C.
Methanesulfonyl chloride (1.15 ml, 14.9 mmol) was added dropwise and the reaction was stirred at 0 OC for 1 h. Saturated sodium bicarbonate was added and the reaction was extracted (x3) with dichloromethane, dried (MgS04), filtered and concentrated in vacuo to give 4-(4-nitrophenyl)-l-methylsulfonylpiperazine as a yellow solid (3.83 g, quantitative yield). GC/MS (EI, m/z 285.
Reference Example 12b: 4-(4-methanesulfonyl-piperazin-1 -yl)-phenylamine.
4-(4-Nitrophenyl)-l-methylsulfonylpiperazine (3.83 g, 13.4 mmol), as prepared in Reference Example 12a above, was mixed in methanol (100 ml) and 2 M ammonia in methanol (50 ml) and 10 palladium on carbon (400 mg) was added. The mixture was hydrogenated on a Paar apparatus (50 psi) for 3 h.
The reaction was allowed to cool, the catalyst was filtered, washed with methanol then washed with chloroform. The chloroform portion contained a minor amount of the desired but looked purer. The chloroform portion was concentrated in vacuo and was recrystallized ethyl acetate to give 4-[4-(methylsulfonyl)-l-piperazinyl]benzenamine as a shiny brown solid (0.94 g, 27 yield, mp 192-193 GC/MS (EI, m/z 255.
Reference Example 13 HN N S -a Preparation of 4-Thiomorpholin-4-yl-phenylamine: Reference Example 13a: 4-(4-Nitro-phenyl)-thiomorpholine.
4-Fluoronitrobenzene (3.0 g, 21.3 mmol) was dissolved in toluene (25 mL). Thiomorpholine (2.4 mL, 23.4 mmol) was added and the mixture stirred overnight at 100 At 17 h, the mixture was distributed between ethyl acetate (100 mL) and saturated sodium bicarbonate WO 02/055014 PCT/SE02/00070 59 mL). The organic layer was separated; dried (Na 2
SO
4 filtered and concentrated under vacuum. The residue was triturated with hexane to yield a bright yellow solid.
Reference Example 13b: 4-Thiomorpholin-4-yl-phenylamine.
4-(4-Nitro-phenyl)-thiomorpholine(3.0g, 13.4 mmol), as prepared in Reference Example 13a above, was dissolved in ethanol (250 mL) and 10% palladium on carbon (250 mg) was added. This mixture was shaken on a Parr hydrogenator for 3 h. The reaction mixture was then filtered through diatomaceous earth and concentrated under vacuum. The residue was triturated with hexane to yield an gray solid (2.1 g).
Reference Example 14
H
2 N 0
O
Preparation of 1-(4-Amino-phenyl)-l-morpholin-4-yl-methanone.
Reference Example 14a: 1-Morpholin-4-yl- -(4-nitro-phenyl)-methanone: 4-Nitrobenzoyl chloride (5 g, 27 mmol) in tetrahydrofuran (10 mL) was added slowly to a solution of morpholine (5g, 88 mmol) and triethylamine (2.7 g, 27 mmol) in tetrahydrofuran (50 mL), and stirred at room temperature for four hours. Ethyl acetate (200 mL) was added to the mixture and the combined mixture was washed with water (25 mL), 1N HC1 (25 mL), water (25 mL), saturated sodium bicarbonate (25 mL), water (25 mL) and brine mL). The mixture was dried (Na2SO4), filtered and concentrated under vacuum and the residue used without further purification.
Reference Example 14b: 1-(4-Amino-phenyl)-l-morpholin-4-yl-methanone.
This compound was prepared from 1-morpholin-4-yl-l-(4-nitro-phenyl)-methanone as prepared in Reference Example 13b.
Reference Example
CN
H
2 N- N- O Preparation of 5-Amino-2-morpholin-4-yl-benzonitrile Reference Example 15a: 2-Morpholin-4-yl-5-nitro-benzonitrile.
3-Cyano-4-fluoronitrobenzene (3.3 g, 19.9 mmol) was dissolved in ethyl acetate mL). Morpholine (2.2 mL, 25 mmol), and N,N-diisopropylethylamine (3.5 mL, 20 mmol) WO 02/055014 PCT/SE02/00070 were added and the mixture stirred overnight at room temperature. At 17 h, additional ethyl acetate (150 mL) was added and the combined mixture was washed with water (50 mL) and brine (50 mL), dried (Na 2
SO
4 filtered and concentrated under vacuum. The residue was used without further purification.
Reference Example 15b: 5-Amino-2-morpholin-4-yl-benzonitrile This compound was prepared from 2-Morpholin-4-yl-5-nitro-benzonitrile (as prepared in Reference Example 15a above), as prepared in Reference Example 13b.
Reference Example 16
F
HN- N O Preparation of 3-Fluoro-4-morpholin-4-yl-phenylamine Reference Example 16a: 4-(2-Fluoro-4-nitro-phenyl)-morpholine.
3,4-Difluoronitrobenzene (3.7 g, 23.2 mmol) was dissolved in ethyl acetate (10 mL).
Morpholine (2.2 mL, 25 mmol), and N,N-diisopropylethylamine (4 mL, 23 mmol) were added and the mixture stirred overnight at room temperature. At 17 h, additional ethyl acetate (150 mL) was added and the combined mixture was washed with water (50 mL) and brine (50 mL), dried (NazSO 4 filtered and concentrated under vacuum. The residue was used without further purification.
Reference Example 16b: 3-Fluoro-4-morpholin-4-yl-phenylamine.
This compound was prepared from 4-(2-Fluoro-4-nitro-phenyl)-morpholine, (as prepared in Reference Example 16a above) as prepared in Reference Example 13b.
Reference Example 17 H2N-N
CH
3 H C CH 3 Preparation of 4-(4-Amino-phenyl)-piperazine-l-carboxylic acid tert-butyl ester: Reference Example 17a: 4-(4-Nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester.
4-Fluoronitrobenzene (4.8 g, 34 mmol) was dissolved in ethyl acetate (25 mL). Piperazine-1carboxylic acid tert-butyl ester (6.7 g, 36 mmol) and N,N-diisopropylethylamine (6.3 mL, 36 mmol) were added and the mixture was stirred at 65 OC for five days and cooled to room temperature. Ether (100 mL) was added and the combined mixture was washed with water WO 02/055014 PCT/SE02/00070 61 mL) and brine (25 mL), dried (Na2SO4), filtered and concentrated under vacuum. The residue was triturated with hexane to yield a bright yellow solid (8 g; 77%).
Reference Example 17b: 4-(4-Amino-phenyl)-piperazine- 1 -carboxylic acid tert-butyl ester.
4-(4-Amino-phenyl)-piperazine-1 -carboxylic acid tert-butyl ester was prepared from 4-(4-Nitro-phenyl)-piperazine-l-carboxylic acid tert-butyl ester, (as prepared in Reference Example 1 7a) as prepared in Reference Example 1 3b.
Reference Example 18 0
H
2 NaNj Preparation of 3-Morpholin-4-yl-plienylarnine Reference Example 18a: 4-(3-Nitro-phenyl)-morpholine.
3-Fluoronitrobenzene (10 g, 71 minol) was dissolved in acetonitrile (100 mL).
Morpholine (30 mL, 350 mmol) was added and the mixture was reacted 18 h at 150 in a pressure reactor. The reaction was cooled to room temperature, concentrated under vacuum and 5g of the total mixture was purified by column chtiomatography on silica eluted with CH 2 Cl 2 The product (3.6 g) was isolated as a bright yellow oil.
Reference Example 1 8b: 3-Morpholin-4-yl-phenylamine 3-Morpholin-4-yl-phenylamine was prepared from 4-(3-Nitro-phenyl)-morpholine, (as prepared in Reference Example 18Sa), as prepared in Reference Example 1 3b.
Reference Example 19 HNN N Preparation of 2-[4-(4-amino-phenyl)-piperazin-1-ylJ-ethanol.
Reference Example 1 9a: 2 [4-(4-nifrophenyl)piperazine- 1 -yl] -ethanol.
2[4-(4-nitrophenyl)piperazine- 1 -yl]-.ethanol is prepared from commcrcially available 4-fluoronitrobenzene (Aldrich) and commercially available N-(2-hydroxyethyl)piperazine (Aldrich) via the same procedure as described in Reference Example 13a above.
Reference Example 19b: 2- [4-(4-amino-phenyl)-piperazin- I -yl] -ethanol.
2-[4-(4-amino-phenyl)-piperazin- 1 -yl]-ethanol is prepared by catalytic hydrogenation of 2 [4-(4-nitrophenyl)piperazine- 1-yl]-ethanol (prepared as in Reference Example 1 9a) as described in Reference Example 1 3b WO 02/055014 PCT/SE02/00070 -62- Reference Example
H
2 N- 0 Preparation of 4-Morpholin-4-yl-phenylamine.
4-(4-Nitrophenyl)morpholine (10.3 g, 49.5 mmol;) (Lancaster Synthesis) was suspended in methanol (130 ml) and 2 M ammonia in methanol (70 mL) and 5 palladium on carbon (100 mg) was added. The mixture was hydrogenated on a Paar apparatus (50 psi) for 1 h. The reaction was allowed to cool, the catalyst was filtered and the solution was concentrated in vacuo. The crude solid was recrystallized from ethyl acetate hexane to give 4-(4-morpholinyl)aniline as a light purple solid (6.2 g, 70 yield, mp 132-133 OC).
GC/MS (EI, m/z 178.
Reference Example 21
HO
H
2 N N O Preparation of 4-Amino-3-hydroxyphenylmorpholine 4-Nitro-3- hydroxyphenylmorpholine (Maybridge Chemical) (3.34 g, 14.9mmol) was dissolved in 59 ml of ethanol at 30 0 C. The mixture was stirred at 25 0 C and treated with tin (II) chloride dihydrate (16.8 grams, 74.5mmol) with stirring. The yellow suspension was heated to reflux over a 30 minute period. TLC showed reaction progress over several hours.
The mixture was refluxed for 18 hours, cooled to room temperature, and concentrated to remove most of the ethanol to give a yellow slurry. The mixture was treated with saturated aqueous sodium bicarbonate until it was basic. The mixture was extracted with ethyl acetate, filtered, and the organic layer was separated. The aqueous layer was extracted twice more with ethyl acetate. The extracts were combined, dried over magnesium sulfate, filtered, and concentrated to give 1.02 grams of a purple solid. Proton NMR and CI mass spectral analyses were consistent for the desired product (m/z 195 base peak by positive ion CI and m/z =193 base peak by negative ion CI).
WO 02/055014 PCT/SE02/00070 -63- Reference Example 22 I 0
N
Preparation of 6-Methoxy-8-(4-methyl-[1,4]diazepan-l-yl)-4-oxo-4H-chromene-2carboxylic acid Reference Example 22a: 6-Methoxy-8-(4-methyl-[1,4]diazepan-1-yl)-4-oxo-4H-chromene-2carboxylic acid ethyl ester.
Into a 250 mL 3 neck round bottom flask equipped with a reflux condenser, nitrogen inlet and magnetic stirrer is placed 1.5 g (4.59 mmol, 1.0 equiv.) of 8-Bromo-6-methoxy-4oxo-4H-chromene-2-carboxylic acid ethyl ester (Reference Example 2c), 84 mg (0.092 mmol, 0.02 equiv.) of tris dibenzylidineacetone dipalladium, 342 mg (0.55 mmol, 0.12 equiv.) of racemic 2,2'-bis(diphenylphosphino)-1,1'-binapthyl and 2 g of 4 A molecular sieves. To this suspension is added 150 mL of dry toluene. To the stirred suspension is then added 628 mg, 684 gL, (5.50 mmol, 1.2 equiv.) of 1-methylhomopiperazine, followed by 2.05 g (6.3 mmol, 1.4 equiv.) of cesium carbonate. The mixture is then heated to 80 OC for 3 days. At the end of this time completion was monitored by LC/MS analysis of an aliquot. When the reaction was determined to be complete it was cooled to room temperature then filtered through a plug of diatomaceous earth with toluene washing to remove solid by products. Purification by flash chromatography, using a gradient of 5 to 20% methanol in methylene chloride as eluent, yielded 1.0 g, of the desired product.
Mass Spec.: calc. for [C 1 9
H
24
N
2 0 5 +H] Theor. m/z 361; Obs. 361 Reference Example 22b: 6-Methoxy-8-(4-methyl-[1,4]diazepan-1-yl)-4-oxo-4H-chromene- 2-carboxylic acid.
Into a 125 mL erlenmeyer equipped with a magnetic stirrer is placed 319 mg (0.89 mmol, 1.0 equiv.) of 6-Methoxy-8-(4-methyl-[1,4]diazepan-l-yl)-4-oxo-4H-chromene-2carboxylic acid ethyl ester. This material is dissolved in 30 mL of THF, then 30 mL of methanol are added. To this stirring solution is added 30 mL of a water containing 41 mg (0.97 mmol, 1.1 equiv.) of lithium hydroxide. This mixture is stirred at room temperature for WO 02/055014 PCT/SE02/00070 -64- 2 hr. Completion of the reaction is monitored by LC/MS, then 10 mL of 2N HCI is added.
This mixture is then concentrated, dried and triturated with ether to give the product as the hydrochloride salt in quantitative yield.
Mass Spec.: calc. for [C17H20N20s+H] Theor. m/z 333; Obs. 333 Reference Example 23 0
O
N) O
N
1 0 Preparation of 6-Ethoxy-8-(4-methyl-piperazin-l-yl)-4-oxo-4H-chromene-2-carbonyl chloride Reference Example 23a: 8-Bromo-6-hydroxy-4-oxo-4H-chromene-2-carboxylic acid ethyl ester: The hydroxy compound, 8-Bromo-6-hydroxy-4-oxo-4H-chromene-2-carboxylic acid ethyl ester, is formed as a side product during the synthesis of 8-Bromo-6-methoxy-4-oxo-4Hchromene-2-carboxylic acid ethyl ester. It can be separated from the crude methoxy compound by flash chromatography using a step gradient of 20% ethyl acetate in methylene chloride to the same solvent containing 2% methanol. The hydroxy compound, which elutes last, is concentrated to give the pure compound. Mass Spec.: calc. for [C1 2 H9Br0 5
+H]
Theor. m/z 313, 315; Obs. 313, 315 Reference Example 23b: 8-Bromo-6-ethoxy-4-oxo-4H-chromene-2-carboxylic acid ethyl ester: Into a 100 mL 3 neck round bottom flask equipped with a reflux condenser, nitrogen inlet and magnetic stirrer is added 700 mg (2.24 mg, 1.0 equiv.) of 8-Bromo-6-hydroxy-4oxo-4H-chromene-2-carboxylic acid ethyl ester (Reference Example 23a). This material is dissolved in 50 mL of toluene, then 689 mg, 586 gL (4.47 mmol, 2.0 equiv.) of diethyl sulfate and 309 mg (2.24 mmol, 1.0 equiv.) of K 2 C0 3 were added. The reaction was then heated to reflux for 24 hr. At the end of this time, monitoring by LC/MS reveals that the reaction is >than 95% complete. The reaction is then cooled, 100 mL of ethyl acetate is added and the organic layer is washed with 0.5N HC1 solution, dried over Na 2
SO
4 filtered and concentrated.
The residues were subjected to flash chromatography, using 40% ethyl acetate in hexane as WO 02/055014 PCT/SE02/00070 eluent. The purified fractions were concentrated to yield 500 mg of a colorless solid.
Mass Spec.: calc. for [C 1 4 H1 3 BrOs+H] Theor. m/z 341, 343; Obs. 341, 343 Reference Example 23c: 6-Ethoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2carboxylic acid ethyl ester: Into a 1OOmL, 3 neck round bottom flask equipped with a reflux condenser, magnetic stirrer and nitrogen inlet is added 350 mg (1.03 mmol, 1.0 equiv.) of 8-Bromo-6-ethoxy-4oxo-4H-chromene-2-carboxylic acid ethyl ester (Reference Example 23b), 18.9 mg (0.02 mmol, 0.02 equiv.) of tris dibenzylidineacetone dipalladium, 77 mg (0.123 mmol, 0.12 equiv.) of racemic 2,2'-bis(diphenylphosphino)-1,l'-binapthyl and Ig of 4 A molecular sieves and mL of dry toluene. To the stirred suspension is then added 113 mg, 1255 pL, (1.13 mmol, 1.1 equiv.) of 1-methylpiperazine, followed by 470 mg (1.44 mmol, 1.4 equiv.) of cesium carbonate. The mixture is then heated to 80 oC for 3 days. At the end of this time completion was monitored by LC/MS analysis of an aliquot. When the reaction was determined to be complete it was cooled to room temperature then filtered through a plug of diatomaceous earth, with toluene washing to remove solid by products. Purification by flash chromatography, using a gradient of 5 to 40% methanol in methylene chloride as eluent, yielded 350 mg of the desired product as a yellow solid. Mass Spec.: calc. for [Cs 1
H
24 Nz 2 O+H] Theor. m/z 361; Obs. 361 Reference Example 23d: 6-Ethoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2carboxylic acid: Into a 125 mL Erlenmeyer equipped with a magnetic stirrer is placed 500 mg (1.39 mmol, 1.0 equiv.) of 6-Ethoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid ethyl ester (Reference Example 23c). This material is dissolved in 30 mL of THF, then mL of methanol are added. To this stirring solution is added 30 mL of a water containing 64.2 mg (1.53 mmol, 1.1 equiv.) of lithium hydroxide. This mixture is stirred at room temperature for 2 hr. Completion of the reaction is monitored by LC/MS, then 10 mL of 2N HC1 is added. This mixture is then concentrated, dried and triturated with ether to give the product as the hydrochloride salt in quantitative yield.
Mass Spec.: calc. for [ClH 2 oN20s+H] Theor. m/z 333; Obs. 333 Reference Example 23e: 6-Ethoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2carbonyl chloride: Into a 100 mL round bottom flask equipped with a reflux condenser, nitrogen inlet and magnetic stirrer is placed 250 mg (0.68 mmol, 1.0 equiv.) of 6-Ethoxy-8-(4-methyl-piperazin- WO 02/055014 PCT/SE02/00070 -66l-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride salt (Reference Example 23d) and mL of methylene chloride. To the stirring suspension is then added 129.5 mg, 164 L(1.02 mmol, 1.5 equiv.) of oxalyl chloride followed by addition of one drop of DMF from a 50 microliter syringe to act as catalyst. The mixture is stirred for 2 hours, then concentrated to dryness on a rotary evaporator under a nitrogen atmosphere, followed by drying under high vacuum. The completeness of the reaction was ascertained by analysis of an aliquot, which was quenched with a THF solution ofmethylamine, by LC/MS. The crude material was used as obtained in the subsequent amidation reaction.
Reference Example 24 0 0
N
Br 0 Preparation of 8-Bromo-6-methoxy-4-(2-trimethylsilanyl-ethoxymethoxy)-quinoline-2carboxylic acid methyl ester.
Reference Example 24a: 2-(2-Bromo-4-methoxy-phenylamino)-but-2-enedioic acid dimethyl ester.
A solution of 2-bromo-4-methoxy aniline (6.02 g, 29.8 mmol) in 125 mL anhydrous methanol was treated with dimethyl acetylenedicarboxylate (3.70 mL, 30.2 mmol) and the solution was heated at reflux under nitrogen for 8 hours. The reaction mixture was cooled, concentrated, and redissolved in hot methanol. Yellow crystals were obtained by filtration (6.93 g, A second crop of crystals was obtained from ethanol (0.942 g, The filtrates were combined and purified by flash chromatography on silica gel using 4:1 hexanes:ethyl acetate to afford an additional 1.63 g for a total yield of 93%. 'H NMR (300 MHz, DMSO, d 6 6 9.60 1 H, NH), 7.26 1 H, Jm 2.7 Hz, ArIf3), 6.93 (dd, 1 H, Jo= 8.7, Jm= 2.7 Hz, ArH 5 6.87 1 H, Jo= 8.7 Hz, ArH 6 5.34 1 H, C=CH), 3.76 3 H, OCH3), 3.68 3 H, CHCO 2 CH3), 3.66 3 H, CNCO 2 CH3); Mass Spec.: calc. for [C1 3 H14BrNOs+H]+ Theor. m/z 344, 346; Obs. 344, 346.
Reference Example 24a: 8-Bromo-6-methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester.
Dow-Therm (175 mL) was heated to 244 'C and the 2-(2-bromo-4-methoxyphenylamino)-but-2-enedioic acid dimethyl ester (9.50 g, 27.6 mmol) was added as a solid in WO 02/055014 PCT/SE02/00070 -67portions over 7 minutes while maintaining a temperature of 230-240 The brown reaction mixture was heated at 240-245 OC for 45 minutes and then cooled to room temperature. A yellow precipitate formed upon cooling. Approximately 100 mL of hexanes were added to the mixture and the solids were isolated by filtration, washed with additional hexanes, and dried under high vacuum to afford the product as a yellow solid (6.73 g, 'H NMR (300 MHz, DMSO, d 6 5 12.01 1 H, NH), 7.86 1 H, Jm 2.7 Hz, ArHfi), 7.52 1 H, C=CH), 7.48 1 H, Jm= 2.7 Hz, ArH 7 3.93 6 H, OCH3 and CO 2 CH3); Mass Spec.: calc. for
[C,
2 HioBrNO 4 +H] Theor. m/z 312, 314; Obs. 312, 314.
Reference Example 24c: 8-Bromo-6-methoxy-4-(2-trimethylsilanyl-ethoxymethoxy)quinoline-2-carboxylic acid methyl ester.
A brown solution of 8-bromo-6-methoxy-4-oxo-1,4-dihydro-quinoline-2carboxylic acid methyl ester 6.73 g, 21.6 mmol) in 100 mL N-methyl pyrolidinone was treated with sodium hydride (60% dispersion in oil, 1.028 g, 25.7 mmol). Gas evolution and warming were observed. The reaction was stirred for 10 minutes at room temperature under nitrogen. Addition of 2-(trimethylsilyl)ethoxymethyl chloride (5.00 mL, 28.3 mmol) resulted in a slightly cloudy, light brown solution. After 2.5 hours at room temperature, the reaction mixture was poured into 800 mL water and stirred for 15 minutes. The resulting cream colored precipitate was isolated by filtration, washed with water, and dried under high vacuum to afford the product as a cream colored solid (9.70 g, quantitative yield). 'H NMR (300 MHz, DMSO, d 6 8 7.976 1 H, Jm= 2.7 Hz, ArH7), 7.79 1 H, 7.53 1 H, Jm= 2.7 Hz, ArH5), 5.70 2 H, OCH20), 3.99 6 H, OCH3 and CO2CH3), 3.88 2 H, J= Hz, OCH 2 CHzSi), 0.97 2 H, J= 8.0 Hz, OCH 2 CH2Si), -0.04 9 H, Si(C H3) 3 Mass Spec.: calc. for [C18H 24 BrNOsSi+H] Theor. m/z 442, 444; Obs. 442, 444.
Reference Example
O
I H N HO Preparation of 6-Methoxy-8-(4-methyl-[1,4]diazepan-l-yl)-4-oxo-1,4-dihydro-quinoline- 2-carboxylic acid.
WO 02/055014 PCT/SE02/00070 -68 Reference Example 25a: 6-Methoxy-8-(4-methyl-[ 1,4] diazepan-l -yl)-4-(2-triinethylsilanylethoxymecthoxy)-quinoline-2-carboxylic acid methyl ester.
To a clear, light brown solution of 2-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid methyl ester (1.01 g, 2.28 mmol), Nmethylhomopiperazine (0.32 mL, 2.57 mmol), and 4 A sieves in 30 mL anhydrous toluene was added Pd 2 (dba) 2 (43.8-mg, 0.048 mmol) and BTNAP (169.8mg, 0.27 mmol). The resulting wine colored solution was treated with cesium carbonate 124 g, 3.45 nimol). The reaction mixture was heated at reflux under nitrogen for 21 hours. The pea green reaction mixture was cooled to room temperature and concentrated. The crude mixture was purified by flash chromatography on silica gel using a gradient of 95:5 to 40:60 methylene chloride: methanol to afford the desired product as a yellow foam (1.004 g, 'H NMR (300 MHz, DMSO, dQ 857.67 1 H, ArmH), 6.94 1 H, Jm 2.4 Hz, A4H.), 6.66 I H, Jm,, 2.4 Hz, Ar H 7 5.60 2 H, OCff2O), 3.94 3 H, C0 2 C~H) 3.88 3 H, OCHR), 3.82 2 H, J= Hz, OC HCH 2 Si), 3.75 (bs, .4 H1, ArNCH,,CH 2
CH
2
NCH-
3 ArNCHCH 2 N-CH3), 3.45 (bs, 2 H, ArNCH 2 CH2NCH 3 3.31 (bs, 2 H, ArNCH 2
CH
2 C H 3 283 (s 3 -,Ni 3 2.8 (bs, 2 H ArNCH 2
CU
2
CH
2
NCH
3 0.92 2 H, J= 8.0 Hz, OCH1 2 CHi 2 -0.04 9 H, Si(C Hi) 3; Mass Spec.: caic. for [C 24
H
37
N
3 0SSi+H]+ Theor. rn/z =476; Obs. 476.
Reference Example 25b: 6-Methoxy-8-(4-methyl-[1I,4]diazepan-1 -yl)-4-oxo- 1,4-dihydroquinoline-2-carboxylic acid.
To a light brown solution of 6-methoxy-8-(4-methyl-[ 1,4] diazepan- I trit-methylsilanyl-ethoxymnethoxy)-quinoline-2-carboxylic acid methyl ester (1.00 g, 2.10 mmol) in 18 mL 3: 1: 1 tetrahydroftiran:mcthanol:water was added lithium hydroxide monohydrate (0.267 g, 6.35 mmol). The reaction mixture was stirred at room temperature for hours, acidified to pH 4 with 1 N HCl, and stirred an additional 20 minutes. The reaction mixture was concentrated and dried under high vacuum to afford an orange foam. 'H NMR (300 MHz, DMS0, d 6 5 11.06 1 H, NW, 7.53 1 H, C=CUW, 7.00 1 H, Jm= 2.4 Hz, Prm) 6.0_,1H m24HAf 7 4.05-3.99 (in, 2 H, ArNCH 2
CH
2
CH
2
NCH
3 3.87 (s, 3 H, OCH 3 3.68-3.60 (in, 2 H, ArNCH7.CH 2
NCH
3 3.54-3.47 (in, 2 H, ArNCH 2 CH2NCH 3 3.41-3.26 (in, 2 H, ArNCH 2
CH
2 CH2NCH 3 2.82 3 H, J= 4.8 Hz, NC~H), 2.46-2.41 (in, 1 H ArNCH 2 CH7CH 2
NCH
3 ),2.30-2.25 (in, 1 H ArNCH 2 C~jgCH2NCH 3 Mass Spec.: calc. for [Cl 7
H
2 lN 3
O)
4 Theor. m/z 332; Obs. 332.
WO 02/055014 PCT/SE02/00070 -69 Reference Example 26 Preparation of 6-Fluoro-8-(4-methyl-piperazin-1-yl)-4-oxo-1,4-dihydro-quinoline-2carboxylic acid.
This compound was prepared via the same procedure described for preparation of Reference Example Reference Example 27 0 0
H
N
N-
NN
Preparation of 6-Methoxy-8-(4-methyl-[1 ,4lcliazepan-l -yl)-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
Reference Example 27a: 8-Bromo-6-methoxy-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid.
To a light brown solution of 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid methyl ester (Reference Example 24c) (4.98 g, 11.3 inmol) in 75 ml 3: 1:1 tetrahydrofuran:methanol:water was added lithium hydroxide monohydrate (1.367 g, 32.6 inmol). The reaction was stirred at room temperature for 5 hours.
The reaction mixture was concentrated and then poured into water. The solution was acidified to p1H 2 with 1 N HCI and the resulting solids were isolated by filtration. The solids WO 02/055014 PCT/SE02/00070 were then suspended in methanol and filtered to afford the desired product (2.6732 g, An additional 0.5768 g of product was obtained from the methanol filtrates. 'H NMR (300 MHz, DMSO, d 6 TFA Shake) 5 7.86 1 H, Jm 2.7 Hz, ArH5), 7.55 1 H, J= 2.7 Hz, ArH 7 7.32 1 H, C=CI, 3.94 3 H, OCH3); Mass Spec.: calc. for [CIIH8BrNO 4 +H] Theor. m/z 298, 300; Obs. 298, 300.
Reference Example 27b: 8-Bromo-6-methoxy-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
To a yellow suspension of 8-bromo-6-methoxy-4-oxo-1,4-dihydro-quinoline-2carboxylic acid (Reference Example 27a) (3.446g, 11.56 mmol), TBTU (9.039 g, 28.15 mmol), and HOBt 3.757 g, 27.8 mmol) in 100 mL dimethylformamide was added 4morpholinoaniline( 2.733 g, 15.3 mmol) and diisopropylethyl amine (8.2 mL, 50.2 mmol).
The resulting marroon solution was stirred at room temperature under nitrogen for 16 hours during which time the reaction became greenish brown and formed a large amount of precipitate. The reaction mixture was filtered and the solids washed with dimethylformamide, water, and methanol. Drying under high vacuum afforded the desired product as a yellow solid (3.09 g, 'H NMR (300 MHz, DMSO, d 6 8 12.13 1 H, NH), 10.18 1 H, C(O)NH), 7.90 1 H, Jm 2.7 Hz, ArH), 7.68 2 H, Jo= 9.0 Hz, ArH2& IH 6 7.63 1 H, C=CH), 7.51 1 H, Jm 2.7 Hz, ArH 7 7.00 2 H, Jo=9.0 Hz, ArHi.&J' 3.94 3 H, OCH3), 3.75 4 H, J= 4.8 Hz, OCH2CH 2 3.10 4 H, J= 4.8 Hz, OCH 2
CH
2 Mass Spec.: calc. for [C 2 iH 2 oBrN 3 0 4 +H] Theor. m/z 458, 460; Obs. 458,460.
Reference Example 27c: 8-Bromo-6-methoxy-4-(2-trimethylsilanyl-ethoxymethoxy)quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
A yellow suspension of 8-bromo-6-methoxy-4-oxo-l,4-dihydro-quinoline-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide (Reference Example 27b) (3.092 g, 6.75 mmol) in 40 mL N-methylpyrolidinone was treated with sodium hydride (60% dispersion in oil, 0.410 g, 10.24 mmol). Gas evolution and warming were observed and the suspension became light brown and almost clear. The reaction was stirred for 10 minutes at room temperature under nitrogen. Addition of the 2-(trimethylsilyl)ethoxymethyl chloride (1.6 mL, 9.1 mmol) resulted in a slightly cloudy, lighter brown solution. After 4.5 hours at room temperature, the reaction mixture was poured into 300 mL water, stirred for 15 minutes and then stored at 0 oC overnight. The solids were. isolated by filtration, suspended in methanol, filtered again, and dried under high vacuum to afford the product as a yellow solid (3.190 g, 'HNMR (300 MHz, DMSO, d 6 5 10.18 1 H, C(O)NH), 7.95 1 H, Jm 2.4 Hz, WO 02/055014 PCT/SE02/00070 71 AsiH 7 7.83 1 H, Arjj 7.69 2 H, 9.0 Hz, ArW'i& _H 6 7.51 1 H, .m 2.7 Hz, Arfi 5 7.00 2 H, Hz, Arffiy&jjH), 5.69 2 H, OCH 2 3.95 3 H, OCHA) 3.85 2 H, J= 8.0 Hz, OCII 2
CH
2 Si), 3.75 4 H, J= 4.7 Hz, OCH 2 N,31 t ,J 4.7 Hz, OCH 2 CHN), 0.94 2 H, J= 8.0 Hz, OCH 2 GHSi), -0.04 9 H, Si(C HD 3 Mass Spec.: 'caic. for [G 27
H
34 BrN 3 OsSi+H]+ Theor. m/z 588, 590; Obs. 588, 590.
Reference Example 27d: 6-Methoxy-8-(4-methYl-[1 ,4]diazepan-1 -yl)-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
To'a yellow-green suspension of 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid (Reference Example 27c) (4-morpholin-4-ylphenyl)-amide 155 g, 1.96 mmol), N-methyl homopiperazine (0.39 mL, 3.14 mmol), and 4 A sieves in 30 mL anhydrous toluene was added Pd 2 (dba) 2 (90.0 mg, 0.098 mmol) and BINAP (0.358 g, 0.58 mmol). The resulting reddish brown mixture became lighter in color upon treatment with cesium carbonate (2.544 g, 7.81 minol). The reaction mnIixture was heated at reflux under nitrogen for 17 hours. The clear brown solution was cooled to room temperature, concentrated, and then purified by flash chromatography on silica gel using a slow gradient of 95:5 to 50:50 methylene chloride:methanol to afford the desired product (0.989 g, 8 1 'H NMR (300 MHz, DMSO, d 6 6 9.88 1 H, NHJ 7.73 1 H, Arjj 3 7.68 2 H, 8.9 H z, Ar H 2
H
6 7.00 2 H, 8.9 Hz, ArH 6.94 1 H, 2.7 Hz, AkHW), 6.66 1 H, Jm 2.7 Hz, ArHE 7 5.62 2 H, OCH 2 3.87 3 H, OC~H), 3.80(t, 2 H, J= 8.0 Hz, OCiH 2 S) 3.3(,4H= 4.7 Hz, OCfiCH 2 3.63 2 H, J= 5.9 Hz, ArNCH7CH 2
CH
2
NCH
3 3.3 3 (bs, 2 H, ArNCH2CH 2
NCH
3 3.09 4 H, J= 4.7 Hz, OCH 2
CII
2 2.97 (bs, 2 H, ArNCH 2 CH2NCH 3 2.69 (bs, 2 H, ArNCH 2
CH
2 CH2NCH 3 2.35 3 H, NCH) 2.9(sB rC 2 zCH 2 NC H 3 0.94 (t, 2 H, J= 8.0 Hz, OCH 2
CH?
2 Si), -0.03 9 H, Si(C 3; Mass Spec.: caic. for
[C
33 H47N 5
O
5 Si+H1+ Theor. nm/z =622; Ohs. =622.
Reference Example 28 WO 02/055014 PCT/SE02/00070 -72 Preparation of 8-Bronio-4-dimethylamino-6-methoxy-quinoline-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide.
Reference Example 28a: 8-Bromo-4-chloro-6-rnethoxy-quinoline-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide.
A suspension of 8-bromo-6-methoxy-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid (Reference Example 27b) (1.75 mmol) in 20 ml, methylene chloride was treated with oxalyl chloride (1.5 mL, 17.2 mmol) and catalytic dimethylformamide (3 drops). The reaction mixture bubbled vigorously and became clearer. The reaction was heated at reflux for 2 hours, cooled to room temperature, and concentrated to a pale yellow solid (kept under nitrogen).
To a yellow solution of the acid chloride in 20 mL methylene chloride was added 4morpholinoaniline (0.347 g, 1.94 mmol) and diisopropylethyl amine (1.0 mL, 6.1 mimol). The solution became orange and gas evolution was observed. Within 30 minutes, solids began to precipitate from the solution. The reaction was stirred at room temperature for 1 hour. The solids were isolated by filtration and dried under high vacuum to afford the desired product (0.406 g, 'H NMR (300 MHz, DMS0, 8 10. 15 1 H, C(0)NH9, 8.33 1 H, 8. 10 1 H, Jm= 2.7 Hz, ArH 7 7.70 2 H, 9. 0 Hz, Axll 2
H
6 7.5 6 I H, 2.7 Hz, Arff), 7.01 2 H, J,=9.0 Hz, Arfiy& 3 H, OCH3), 3.75 4 H, J 4.8 Hz, OCfiCH 2 3.11 4 H, J= 4.8 Hz, OCH 2 Cfl2N); Mass Spec.: cale, for
[C
21 H, gBrClN 3
O
3 Theor. m/z =476, 478; Obs. 476, 478.
Reference Example 28b: 8-Bronio-4-dimethylamino-6-methoxy-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
A solution of 8-bromo-4-chloro-6-methoxy-quinoline-2-carboxylic acid (4-morpholin- 4-yl-phenyl)-amide (Reference Example 28a) (0.1512 g, 0.3 17 mmol) in 100 mL 2.0 M dimethyl amine in tetrahydrofuran was heated at 100 'C in a Parr bomb. The initial pressure was 75-80 psi and then remained at approximately 60 psi. After 18 hours, the reaction was cooled to room temperature, concentrated and dried to afford the crude product as a brown solid. Purification on silica gel using a gradient of 100:0 to 95:5 methylene chloride:methanol afforded the clean product 142 g, 920/o). 'H NMR (3 00 MHz, DMSO0, dQ 5 10.20 1 H, C(0)NEi), 7.90 1 H, Jm= 2.7 Hz, Arfi 7.69 2 H, 9.0 Hz, Arff'& H' 7.60 1 H, ArH3), 7.41,(d, 1 H, Jm 2.7 Hz, Arl') .1(H 0 z ArH 3 &j 3.96 3 H, 3.75 4 H, J= 4.8 Hz, OCli 2
CH
2 3. 10 4 H, J= 4.8 Hz, OCH 2
CII
2 3.08 WO 02/055014 PCT/SE02/00070 -73- 6 H, N(CH3) Mass Spec.: calc. for [C 2 1H19BrClN 3 0 3 +Hf] Theor. m/z 485, 487; Obs. 485, 487 Reference Example 29 0/ F
N
Preparation of 6-Fluoro-4-methoxy-8-(4-methyl-piperazin-l-yl)-quinoline-2-carboxylic acid Reference Example 29a: 8-Bromo-6-fluoro-4-methoxy-quinoline-2-carboxylic acid methyl ester Into a 150 mL 3 neck round bottom flask equipped with a reflux condenser, magnetic stirrer and nitrogen inlet is placed 2.0 g (6.76 mmol, 1.0 equiv.) of 8-Bromo-6-fluoro-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid methyl ester. This material is then dissolved in mL of NMP. Then 300 mg (7.44 mmol, 1.1 equiv.) of a 60% dispersion of sodium hydride in oil is cautiously added portion-wise to the solution at room temperature. A yellow color then develops, indicating that formation of the anion has occurred, with hydrogen evolution.
Stirring of the anion solution is continued for one hour, then 1.14 g, 500 gL (8.04 mmol, 1.2 equiv.) of iodomethane is added via syringe. The mixture is allowed to react for two hours additional, then is cautiously quenched with 20 mL of water. The solids, which precipitate upon dilution in 1L of water, are collected by filtration, then washed with water to give the pure O methylated material as 2.1 g of a colorless solid.
Mass Spec.: calc. for [Cz 1
H
9 BrFNO 3 Theor. m/z= 314, 316; Obs. 314, 316 Alternatively, into a 100 mL 3 neck round bottom flask equipped with a reflux condenser, nitrogen inlet and magnetic stirrer is placed 350 mg (1.17 mmol, 1.0 equiv.) of 8- Bromo-6-fluoro-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid methyl ester and 242 mg (1.75 mmol, 1.5 equiv.) of K 2 C0 3 This material is suspended in 20 mL of DMSO then heated to 70 oC for 1 hr. The anion formation of the anion is apparent when the mixture becomes cloudy. The mixture is allowed to cool to 35 OC then 331 mg, 145 gL (2.33 mmol, equiv.) of methyl iodide are added and stirring is continued for 2 hr. At the end of this WO 02/055014 PCT/SE02/00070 -74time it is determined if the reaction is complete by LC/MS. Upon completion the mixture is poured into 200 mL of water and the solids which form are collected by filtration and washed with water to give 340 mg of the Q-methylated product after drying.
Reference Example 29b: 6-Fluoro-4-methoxy-8-(4-methyl-piperazin-1-yl)-quinoline-2carboxylic acid methyl ester Into a 250mL, 3 neck round bottom flask equipped with a reflux condenser, magnetic stirrer and nitrogen inlet is added 2.1 g (6.68 mmol, 1.0 equiv.) of 8-Bromo-6-fluoro-4methoxy-quinoline-2-carboxylic acid methyl ester (Reference Example 29a) (122 mg, 0.134 mmol, 0.02 equiv.) oftris dibenzylidineacetone dipalladium, 499 mg (0.802 mmol, 0.12 equiv.) of racemic 2,2'-bis(diphenylphosphino)- 1,1'-binapthyl and 1 g of 4 A molecular sieves and 80 mL of dry toluene. To the stirred suspension is then added 736 mg, 815 gL, (7.35 mmol, 1.1 equiv.) of 1-methylpiperazine, followed by 3.05 g (9.35 mmol, 1.4 equiv.) of cesium carbonate. The mixture is then heated to 80 oC for 36 hr. At the end of this time completion was monitored by LC/MS analysis of an aliquot. When the reaction was determined to be complete it was cooled to room temperature then filtered through a plug of celite, with toluene washing to remove solid by products. Purification by flash chromatography using a gradient of 5 to 20% methanol in methylene chloride as eluent yielded 2.0 g, of the desired product. Mass Spec.: calc. for [Cl7H 2
FN
3 0 3 +H] Theor.
m/z 334; Obs. 334 Reference Example 29c: 6-Fluoro-4-methoxy-8-(4-methyl-piperazin-1-yl)-quinoline-2carboxylic acid Into a 125 mL erlenmeyer flask containing 30 mL of THF and 30 mL of methanol is placed 2.1 g (6.3 mmol) of 6-Fluoro-4-methoxy-8-(4-methyl-piperazin- -yl)-quinoline-2carboxylic acid methyl ester (Reference Example 29b). To this solution is added with stirring 30 mL of water in which is dissolved 291 mg (6.9 mmol, 1.1 equiv.) of lithium hydroxide monohydrate. This solution is allowed to react for 1 hr then is quenched with 10 mL of 2N HC1 solution. The solution is then filtered and the solidswashed with 10 mL of 0.5 N HC1 solution. The combined filtrates are then concentrated to give 2.15 g, of the solid yellow product as the hydrochloride salt. Mass Spec.: calc. for [C 1 6
H
1 8
FN
3 03+H] Theor. m/z 320; Obs. 320 WO 02/055014 PCT/SE02/00070 Example 1 0
N
0
NN
8-(4-methyl- 1-pip erazinyl)-N-[4-(4-morpholinyl)phenyl]-4-oxo-4H-chromene-2carboxamide.
8-(4-methyl- 1 piperazinyl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 1) (400 mg, 1.23 mmol) was suspended in anhydrous NNdimethylformamide (20 ml) and triethylamine (0.69 ml, 4.92 nimol) was added to give a clear solution. The following were added in order: 1 -hydroxybenzotriazole (HOBt (205 mg, mol)), 1H-B enzotriazol- 1 yl)-N,N,N',N?-pentamethylenc-uronium tetrafluoroborate (TBTU (435 mg, 3.1 inmol)) then 4-(dimethylamino)pyridine (25 mg). After stirring for 5 min at room temperature, 4-(4-morpholinyl)aniline (Reference Example 21) (220 mg, mmol). The reaction stirred overnight at room temperature. The solution was concentrated in vacuo, the remains were partitioned between chloroform saturated sodium bicarbonate, extracted (x3) with chloroform, dried (MgS 04) and concentrated in vacuo to give the crude product.
Chromatography on silica (230 400 mesh ASTM) and eluting ethyl acetate followed by 2.5-5% methanol chloroform gave 190 mig yield) of 8-(4-methyl- 1 -piperazinyl)-N- [4-(4-morpholinyl)phenyl]-4-oxo-4H-benzochromene-2-carboxarmide as a yellow solid (mp 217-2180 decomposition and melt 244-247C). LCIMS m/z 449.
WO 02/055014 WO 02/55014PCT/SE02/00070 -76 Example 2 I-[4-(2-Methoxy-phenyl)-piperazin- 1 -yl]-methanoyl}-8-(4-methyl-piperazin- 1l-yl)cljromen-4-one.
This compound was prepared from 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene- 2.-carboxylic acid hydroc hloride (Reference Example 1) and commercially available 1 Methoky-phenyl)-piperazine (Aldrich) via the same procedure used in example 1, yielding'a yellow solid. MS ni/z 463.
Example 3 o 0NN NN 0 101 1-Acetyl-2,3 -dihydro- lH-indol-6-yl)-piperazin-l -yl]-methanoyl }-8-(4-methylpiperazin-1 -yi)-chromen-4-one.
This compound was prepared from 8-(4-Methyl-piperazin- 1 -yi)-4-oxo-4H-chromnene- 2-carboxylic acid hydrochloride (Reference Example and 1 -(6-Piperazin-1I-yl-2,3-dihydroindol- 1-yl)-ethanone (Reference Example 8) as prepared in Example 1, yielding a yellow solid. MS ni/z 516.
WO 02/055014 WO 02/55014PCT/SE02/00070 -77 Example 4 2-Chloro-5-(4- 1 -[8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromen-2-yl]-xnethanoyl piperazin- 1 -yl)-benzonitrile.
This compound was prepared from 8-(4-Methyl-piperazin-l -yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 2-chloro-5-piperazin-1-yl benzonitrile (Reference Example 9) as prepared in Example 1, yielding a yellow solid. MS m/z 493.
00 0N N 0 101 2-f{ 1-[4-(4-Methoxy-phenyl)-piperazin- I -yl]-methanoyl}-8-(4-methyl-piperazin- 1-yl)cbromen-4-one.
This compound was prepared from 8-(4-Methyl-pipcrazin- 1 -yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available (Aldrich) 1 -(4-Methoxy-phenyl)-pipetazine as prepared in example 1, yielding a yellow solid. MS nilz 463.
WO 02/055014 WO 02/55014PCT/SE02/00070 -78- Examiple 6 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic. acid (5-furan-2-yb- 1 H-pyrazol- 3-yl)-amide.
This compound was prepared from 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2carboxylic acid hydrochloride (Reference Example 1) and commercially available 5-furan-2yl- lH-pyrazol-3-ylamine (Maybridge) as prepared in example 1, yielding a yellow solid. MS m/z =420.
Example 7 0 qo N0N 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromeni -2-carboxylic acid (4-imidazol- 1 -yl-phenyl)amide.
This compound was prepared from 8-(4-Methyl-piperazin-lI-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available 4imidazol-1 -yl-phenylamine (Aldrich) as prepared in Example 1, yielding a yellow solid. MS (M-1-H)m/z 430.
WO 02/055014 PCT/SE02/00070 -79 0 N 0 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4-fl ,2,3]thiadiazol-5-ylphenyl)-amide.
This compound was, prepared from 8-(4-Methyl-piperazin-lI-y)-4-oxo-4H-chromenc- 2-carboxylic acid hydrochloride (Reference Example 1) and 1,2,3]thiadiazol-5-ylphenylamine (Reference Example 10) as prepared in Example 1, yielding a yellow solid. MS (M+H)MlZ= 448.
Example 9 0 0
IN
N 0 N
N)
8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid 1,2,3]thiadiazol-5-ylbenzylamide.
This compound was prepared from 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4J1-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available (Maybridge) 4-[-1,2,3]thiadiazol-5-yl-benzylamine as prepared in Example 1, yielding a yellow solid. MS m/z 462.
WO 02/055014 PCT/SE02/00070 807- Example 0
N
K> 0
NN
0 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid [4-(4-acetyl-piperazin- I1yl)-phenyl]-amide.
This compound was prepared from 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 1 -[4-(4-amino-phenyl)-piperazin- 1 -yl] -ethanone (Reference Example 11) as prepared in Example 1, yielding a yellow solid.
MS m/z499.
Example 11 0
NN
zn 1 0 8-(4-Methyl-piperazin- l-yl)-4-oxo-4H-chromene-2-carboxyic acid [4-(4-methanesulfonylpiprain 1-yl)-phenyl] -amide.
This compound was prepared from 8-(4-Metbyl-piperazin- 1 -yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 4-(4-methanesulfonyl-piperazin- 1 -yl)-phenylamine (Reference Example 12) as prepared in Example 1, yielding a yellow solid.
MS nilz 526.
WO 02/055014 PCT/SE02/00070 81 Example 12 0
NN
N)
8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (2-methoxy-4-morpholin- 4-yl-phcnyl)-amide.
8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 1) (0.10 g, 0.3Smmol), HOBt (0.10 g, O.7mmol), TBTU (0.225 g, 0. 7mmol),. 4-(dimethylamino) pyridine 01 g, catalytic amount), triethylamine 15 mL, 1 .04mnrol), and commercially available 2-methoxy-4-morpholin-4-yl-phenylamine (SALOR) 08 g, 0.38mmol) were dissolved in dimethylformamnide (2.5 mL) and stirred at room temperature overnight. Ethyl acetate (150 mL) was added and the resulting mixture was washed with water (3 x 50 mL), dried (Na 2 SOA) filtered, concentrated under vacuum and triturated with ether to yield a yellow solid (85 mg, LCMS: m/z =480.3 Example 13 0 oN
C
N 0 00 N0 8-(4-Methyl-piperazin-1I-yl)-4-oxo-4H-cbromene-2-carboxylic acid (3-chloro-4-morpholin-4yl-phenyl)-ainide.
This compound was prepared from 8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available 3-chioro- 4-morpholin-4-yl-phenylamine (Maybridge) as prepared in Example 12, yielding a yellow solid. (110mg LCMS m/z =483.5 WO 02/055014 Example 14 PCT/SE02/00070 82
SN
8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H-chromcne-2-carboxylic acid (4-thiomorpholin-4-ylphenyl)-amide.
This-compound was prepared from 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 4-thiomorpholin-4-ylphenylamnine (Reference Example 13) as prepared in Example 12, yielding a yellow solid. mg LCMS m/z =465.5 Example 0 0
NN
100 8 -(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (2,5 -diethoxy-4morpholin-4-yl-phenyl)-amide.
This compound was prepared from 8-(4-Methyl-piperazin-l1-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available diethoxy-4-morpholin-4-yl-phenylanmine (Aldrich) as prepared in Example 12, yielding a yellow solid. (80 mg LCMS nt/z =537.6 WO 02/055014 WO 02/55014PCT/SE02/00070 83 Example 16 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H1-chromene-2- Carboxylic acid (4-cyanomethyl-phenyl)amide.
This compound was prepared from 8-(4-Methyl-piperazin-1I-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available (4amino-phenyl)-acetonitrile (Aldrich) as prepared in Exa mple 12, yielding a yellow solid. mg LCMS lz 403.5 Example 17
(N)
N
8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H--cbromene-2-carboxylic acid (1 This compound was prepared from 8-(4-Methyl-piperazin-lI -yl)-4-oxo-4H-'chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available 1H- (Aldrich) as prepared in Example 12, yielding a yellow solid. (35 mg LCMS mlz401.6 Example 18 0 0 0 N 0 WO 02/055014 PCT/SE02/00070 84 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid -morpholin-4-ylmethanoyl)-phenyl]-amide.
This compound was prepared from 8-(4-Methyl-piperazin-lI-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 1 -(4-amino-phenyl)- I1morpholin-4-yl-methanone (Reference Example 14) as prepared in Example 12, yielding a yellow solid. (21 mg LCMS mlz =477.6 Exaimple 19, 0 0% CN)
N
0 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4fl-chromene-2-carboxylic acid [4-(2,6-dimethylmorpholin-4-yl)-phenyl]-amide.
This compound was prepared from 8-(4-Methyl-piperazin-l-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available 4-(2,6dimethyl-morpholin-4-yl)-phenylamine (Maybridge) as prepared in Example 12, yielding a yellow solid. (60 mg LCMS mlz 477.6 Example 0 0 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4fl-chromene-2-carboxylic acid [4-(4-fluoro-phenoxy)phenyl]-amide.
This compound was prepared from 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-cbromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available 4-(4- WO 02/055014 PCT/SE02/00070 fluoro-phenoxy)-phenylamine (Maybridge) as prepared in Example 12, yielding a yellow solid. (110 mg LCMS m/z 475.6 Example 21 0 o 0 N NO
N
8-(4-Methyl-piperazin-1-yl)-2-(6-morpholin-4-yl-benzooxazol-2-yl)-chromen-4-one.
8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 1) (0.532 g, 1.85mmol) was placed in a 25 mL 3-neck flask under nitrogen and treated with PPA (6 The mixture was then treated with the prepared intermediate 4-amino-3-hydroxyphenylmorpholine (0.43 g of ~85% pure, ~2mmol). The mixture was stirred and heated in an oil bath to 205 0 C for 3 hours to give a dark liquid. The mixture was cooled to room temperature and treated with 10 mL of water to give a dark solution. The solution was slowly neutralized with IN aqueous sodium hydroxide to pH~7 as a solid formed. The solid was collected, washed several times with water, air dried, and vacuum dried at room temperature to give 0.65 g of a black solid. TLC (10%MeOH in CHC13 on SiO 2 showed 2 major components at Rf-0.5 and several lower Rf minor components. The solid was triturated with saturated aqueous sodium bicarbonate at room temperature. It was filtered off, washed several times with water, and air dried to give 0.65 g of a dark gray solid.
TLC showed the same components seen previously. Mass spectral analysis showed m/e 447 by positive ion CI and m/e 446 by negative ion CI. The solid was dissolved in 2% methanol in chloroform and it was chromatographed on a Megabond Elute silica gel column (10 g of SiO 2 using 2% methanol in chloroform. The slightly faster Rf yellow component was concentrated to give 0.0188 g of a yellow solid. CI mass spectral analysis showed m/e 447 as the base peak by positive ion CI. The solid was recrystallized in methanol to give 0.0178 g of a yellow solid with a melting point of 158.1-158.8-°C. Proton NMR (CDC1 3 and CI mass spectral analyses were consistent for the desired product (m/z 447 base peak by positive ion CI and m/z 446 base peak by negative ion CI).
WO 02/055014 PCT/SE02/00070 -86- Example 22 0
OH
O
N
N 01
NN
8-(4-Methyl-piperazin-l-yl)-4-oxo-4H-chromene-2-carboxylic acid (2-hydroxy-4-morpholin- 4-yl-phenyl)-amide.
8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 1) (0.3768 g, 1.16 mmol) was placed in a 100 mL 3-neck flask under nitrogen and it was dissolved in 20 mL of DMF. The solution was treated with triethylamine (0,49mL, 3.5mmol) followed by HOBT hydrate (0.36g, 2.3mmol) followed by TBTU (0.74 g, 2.3mmol) and then followed by DMAP (0.020 The mixture was stirred for 10 minutes and then it was treated with 4-amino-3-hydroxyphenylmorpholine (Reference example 21) (0.228 g, 1.17 mmol). The mixture was stirred for 15 minutes and then it was treated with triethylamine (0.17 mL, 1.2 mmol). The mixture was stirred at room temperature for 42 hours and then it was added to a solution of 50 mL of saturated aqueous sodium bicarbonate and 50 mL of water. The mixture was extracted 4 times with ethyl acetate, dried over magnesium sulfate, filtered, and concentrated to give 0.834 gram of a purple oil. The oil was dissolved in 2 percent methanol in chloroform and it was placed on a silica gel column cm diameter by 10.5 cm long) and eluted with 2 percent methanol in chloroform followed by percent methanol in chloroform. The yellow fraction was concentrated to give 0.2031 gram of an orange-yellow solid. The solid was dissolved in methanol, filtered through a medium sintered glass funnel, and concentrated to a few ml volume as a solid formed. The solid was filtered off, washed with methanol, and air dried to give 0.1613 gram of a tan solid with MP of 248.4 249.6°C. Proton COSY NMR and CI mass spectral analyses were consistent for the desired product (m/z 465 by positive ion CI and m/z 463 by negative ion CI).
WO 02/055014 WO 02/55014PCT/SE02/00070 87 Example 23 a 8-(4-Methyl-piperazin-l1-yl)-4-oxo-4H-chromene-2-carboxylic acid (5-ethoxy-benzothiazol-2yl)-.amide.
This compound was prepared from 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chrom'ene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available benzothiazol-2-ylamine (SALOR) as prepared in Example 12, yielding a yellow solid. (55 mg LCMS -mz 465.3 Example 24
NC)
100 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chrornene-2-carboxylic acid (4-bromo-phenyl)-amide.
This compound was prepared from 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and commercially available 4-bromophenylamine (Aldrich) as prepared in Example 12, yielding a yellow solid. (1.0 g LCMS mlz=442.4 WO 02/055014 PCT/SE02/00070 -88- Example
O
8-(4-Methylpiperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid methyl-(4-morpholin-4-ylphenyl)amide.
8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin-4yl-phenyl)-amide (Example 1) (0.1046 g, 0.2332 mmol) was placed in a 10 mL single neck round flask under nitrogen. The solid was dissolved in 2.8 mL of anhydrous DMF. The yellow solution was stirred at room temperature and treated with one portion of sodium hydride (0.011 g of 95%, 0.44 mmol). The mixture evolved gas and became a red solution. It was stirred under nitrogen for 20 minutes and then it was treated with iodomethane (0.015 mL, 0.033 g, 0.233 mmol). The mixture was sealed and stirred at room temperature for 18 hours.
The reaction mixture was concentrated to remove most of the DMF (35 C bath mm) to give a dark semisolid. It was treated with a few drops of water followed by 10 mL of ethyl acetate. The mixture was dried over magnesium sulfate, filtered, and concentrated to give 0.0564 gram of a yellow glass. The glass was triturated with diethyl ether, filtered off, and dried under high vacuum to give 0.0302 g of a tan solid with MP of 245.0 246.8 C.
Proton NMR and CI mass spectral analyses were consistent for the desired product (m/z 463 by positive ion CI).
Example 26 WO 02/055014 PCT/SE02/00070 89 8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (3-morpholin-4-ylphenyl)-amide.
This compound was prepared from 8-(4-Methyl-piperazin-1-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 3-morpholin-4-yl-phonylamine (Reference Example 18) as prepared in Example 12, yielding a yellow solid. (120 mg LCMS mlz =449.5 Example 27 0
N)
8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (3-cyano-4-morpholin-4yl-phenyl)-amide.
This compound was prepared from,8-(4-Methyl-piperazin- yl)-4-oxo-4H4-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 5-amino-2-morpholin-4-ylbenzonitrile (Reference Example 15) as prepared in Example 12, yielding a yellow solid. (120 mg 82/o),LCMS m/z=474.5 Example 28 0.
N F CZ 0 8-(4-Metliyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (3-fluoro-4-morpholin-4yl-phenyl)-amide.
This compound was prepared from 8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H-cbromene- 2-earboxylic acid hydrochloride (Reference Example 1) and 3-fluoro-4-morpholin-4-yl-' phenylamine (Reference Example 16) as prepared in example 12, yielding a yellow solid.
(120 mg LCMS m/z =467.6 WO 02/055014 PCT/SE02/00070 Example 29 0 N0 1-[8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-cliromen-2-yl]-methanoyl)-amino)-pheny]piperazine-l-carboxylic acid tert-butyl ester.
This compound was prepared from 8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene- 2-carboxylic acid hydrochloride (Reference Example 1) and 4-(4-amino-phenyl)-piperazine- 1 -carboxylic acid tert-butyl ester (Reference Example 17) as prepared in example 12, yielding a yellow solid. (260 mg =5 LCMS m/z =548.6 Example 0
'N
N N 'N 100 8-(4-Methyl-.piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-piporazin- P-ylphenyl)-amide.
1[8-(4-Methyl-piperazin- 1 -yl)-4-oxo-411-chromen-2-yl] -methanoyl} -amino)phenyl]-piperazine-1-carboxylic acid tert-butyl ester (Example 29) (160 mg, 0.3 mmol) was dissolved ethyl acetate (20 mL) and cooled to 0 0 C. HCl gas was bubbled in slowly for 2 minutes. A solid began to precipitate. Methanol (3-4 mL) was added-to dissolve this solid and HOL gas was bubbled in for another 2 minutes. The mixture was concentrated under reduced pressure and triturated with ether and dried under vacuum to yield a tan solid (100 mg, LCMS/ mlz 448.6 WO 02/055014 PCT/SE02/00070 -91- Example 31 0
IN
N 0
NN
6-Methoxy-8 -(4-methyl-piperazin- 1 -yl)-4-oxo-4H-cbromene-2-carboxylic acid (4-morpholin- 4-yl-phenyl)-amide: 6-Methoxy-8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 2) 3 .0g, 8.5 mmol), TBTU (5.5g, 17 mmol), 1hydroxybenztriazole (2.6g, 17 mmol), 4-dimethylaminopyri*dine (0.05g, catalytic) and commercially available 4-morpholin-4-yl-aniline (1.66g, 9.3 mmol) were dissolved in dimethylformamide (100 mL). Triethylamine 3.5 mL, 25 mmol was added and this mixture stirred at room temperature for 17 hours. The reaction mixture was concentrated under vacuum and the residue was partitioned between chloroform (400 mL) and saturated aqueous sodium bicarbonate (50 mL). The organic layer was separated, dried (Na 2
SO
4 vacuum-filtered and concentrated under vacuum. The residue was purified by chromatography on silica eluted with 2methanol in chloroform and then triturated with ether to yield a yellow powder. (1.6 g =39%) LCMS m/z =479.5 mp 234-236'C.
Example 32 0 K- Nj N 0
N
KNII
00 6-Methoxy-8-(4-niethyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid methanesulfonyl-piperazin- 1 -yl)-phenyl]-amide.
This compound was prepared from 6-Methoxy-8-(4-methyl-piperazin-lI-yl)-4-oxo-44cbromene-2-carboxylic acid hydrochloride (Reference Example 2) and 4-(4-methanesulfonyl- WO 02/055014 PCT/SE02/00070 -92 piperazin- I -yl)-phenylamine (Reference Example 12) as prepared in example 1, yielding a yellow solid. GO/MS (El, m/z 556 Example 33 0 IN CI
NN
6-Methoxy-8-(4-Methyl-piperazin- 1-yl)-4-oxo-4H-chrornene-2-carboxylic acid (3-chloro-4morpholin-4-yl-phenyl)-amide.
This compound was prepared from 6-Methoxy-8-(4-methyl-piperazin-l-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and commercially available 3-chloro-4-morpholin-4-yl-phenylamine (Maybridge) as prepared in Example 12, yielding a yellow solid. (45mg= 31%) LCMS mz =513.5 Example 34 0 N aF o 0 0 N 6-Methoxy-8-(4-methyl-piperazin- 1-yl)-.4-oxo-4H-chromene-2-carboxylic acid (3-fluoro-4morpholin-4-yl-phenyl)-amide., This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin-lI-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and 3 -fl-uoro-4-morpholin- 4-yl-phenylamine (Reference Example 16) as prepared in Example 12, yielding a yellow solid. (55mg =6 LCMS m/z 497.5 WO 02/055014 WO 02/55014PCT/SE02/00070 -93 Example 6-Methoxy-8-(4-nethyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (2-methoxy-4morpholin-4-yl-phenyl)-amide.
This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and conmmercially available 2-methoxy-4-morpholin-4-yl-phenylamine (SALOR) as prepared in Example 12, yielding a yellow solid. (55mg LCMS mlz 510.5 Example 36 0 00 N
N
oNN *6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4thiomorpholin-4-yl-phenyl)-amide.
This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin-l -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and 4-thiomorpholin-4-ylphenylamine, (Reference Example 13) as prepared in Example 12, yielding a yellow solid.
(99mg LCMS mn/z 495.5 WO 02/055014 WO 02/55014PCT/SE02/00070 -94 Example 37 6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chrornene-2-carboxylic acid dimethyl-morpholin-4-yl)-plienyl]-amide.
This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and commercially available 4-(2,6-dimethyl-morpholin-4-yl)-phenylamine (Maybridge) as prepared in Example 12, yielding a yellow solid. (70mg LCMS mlz 507.5 Example 38 rl 0 6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (3-morpholin- 4-yl-phenyl)-amide.
This compound was prepared from 6-methoxy-8-(4-Metliyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and *3 -morpholin-4-ylphenylamine (Reference Example 18) as prepared in Example 12, yielding a yellow solid.
LCMS tn/z 479.5 WO 02/055014 WO 02/55014PCT/SE02/00070 Example 39 6-Methoxy-8-(4-methyl-piperazin 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid hydroxy-ethyl)-piperazin- 1 -yl] -phenyl} -amide.
This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and 2-[4-(4-aminophenyl)-piperazin- I -yl] -ethanol (Reference Example 19) as prepared in Example 12, yielding a yellow solid. (80mg mp 211.5-212.2 MS base peak at ml/z =492 by positive ion and mlz =490 by negative ion CI Example 0 0 N 0' 00 6-Methoxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid mnorpholin-4-yl-mnethanoyl)-phenyl]-amide.
This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin-l -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and I -(4-amino-phenyl)- 1niorpholin-4-yl-methanone (Reference Example 14) as prepared in Example 12, yielding a yellow solid. (170mg LCMS mlz 507.5 WO 02/055014 PCT/SE02/00070 -96 Example 41 0
~N
0 CN 0
ND
6-Methoxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-clromene-2-carboxylic acid (3-cyano-4morpholin-4-yl-phenyl)-amnide.
This compound was prepared from 6-methoxy-8-(4-Methyl-piperazin- 1 -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 2) and 5-amino-2-morpholin- 4-yl-benzonitrile (Reference Example 15) as prepared in Example 12, yielding a yellow solid.
(120mg LCMS m/z =504.5 Example 42 0 0 0 1 NN N~ 0 100 4[-f1 -[6-Methoxy-8-(4-niethyl-piperazin- 1-yl)-4-oxo-411-chromen-2-yl]-methanoyl amino)-phenyl] -piperazine-l1-carboxylic acid tert-butyl ester.
The 6-mnethoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 2) (1.04 g, 2.93 mmol) was placed in a 250 ml 3-neck flask under nitrogen and it was dissolved in 50 ml of DMF. The solution was treated with triethylamine (1.22 mL, 8.79 mrnol) followed by HOBT hydrate (0.90 g, 5.9 mmnol) followed by TBTU (1.88 g, 5.9 mmol) and then followed by DMAP (0.056 g, 0.46 mmol). The mixture was stirred for 10 minutes and. then it was treated with 4-(4-Amino-phenyl)-piperazine-1 carboxylic acid tert-butyl ester (Reference Example 17) (0.81 g, 2.9 mmol). The mixture was stirred for 15 minutes and then it was treated with triethylamine (0.41 mL, 2.9 mmol). The mixture was stirred at room temperature for 18 hours and then it was concentrated (1 mm Hg WO 02/055014 PCT/SE02/00070 -97pressure, 45 C bath) to give a dark liquid. The concentrate was treated with 80 mL of saturated aqueous sodium bicarbonate and extracted with ethyl acetate forming a suspended yellow solid in the organic layer. The solid was filtered off, washed with diethyl ether, washed with water, and vacuum dried (0.1mm Hg pressure 25C) to give 0.36 gram of a yellow solid, M.P. 232.3-232.8 C.
Proton NMR and CI mass spectral analyses were consistent for the desired product (m/e 578 by positive ion CI and m/e 576 by negative ion CI).
The aqueous layer was extracted twice with ethyl acetate, dried over magnesium sulfate, filtered, and concentrated to give 1.35 gram of a dark semisolid. It was triturated with diethyl ether and allowed to stand at room temperature as a solid formed. The solid was filtered off, washed with diethyl ether, and vacuum dried at room temperature to give 0.4816 gram of a yellow solid. CI mass spectral analyses was consistent for the desired product (M/Z 578 BY positive ion CI AND M/Z 576 by negative ion CI).
WO 02/055014 PCT/SE02/00070 -98- Example 43 0 N
NH
6-Methoxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-piperazin- I -yl-phenyl)-amide.
The 1-[6-Methoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromen-2-yl]methanoyl}-amino)-phenyl]-piperazine-l-carboxylic acid tert-butyl ester (Example 42) (0.792 gram, 1.37 mmol) was placed in a 50 ml round flask under nitrogen and it was dissolved in ml of methylene chloride. The solution was treated with 15 ml of trifluoroacetic acid (195 mmol) to give a dark solution and it was stirred at room temperature for 18 hours. It was concentrated to give a brown foam. The foam was treated with 30 ml of saturated aqueous sodium bicarbonate and it was stirred at room temperature as a yellow solid formed. The solid was filtered off, washed several times with water, air dried and dried under high vacuum (0.1 mm Hg pressure) to give 0.493 gram.ofa yellow solid, M.P. 203.6-204.7 C.
Proton NMR and CI mass spectral analyses were consistent for the desired product (m/z 478 by positive ion CI and m/z 476 by negative ion CI).
Example 44-54 The following examples were prepared in parallel by acylation of 6-methoxy-8-(4methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-piperazin-1 -yl-phenyl)amide (Example 43) in an Argonaut Quest synthesizer.
The piperazine side chain was derivatized in parallel fashion using eleven different commercially available acylating and sulfonating reagents. The resins used were Argonaut Tech polystyrene amine resins. Each 5 ml Quest tube was charged with 0.010 gram (0.021 mmol) of the starting N-H piperazine and 3ml of methylene chloride followed by 4 equivalents (0.08 mmol) of PS-DIEA resin (diisopropylbenzylamine PS resin) to scavenge HC1. Each tube was then treated with an acyl chloride, sulfonyl chloride, or isocyanate (2 equivalents of each) followed by a little more methylene chloride. The tubes were sealed under nitrogen, and stirred for 3 hours at room temperature. The mixtures were then opened WO 02/055014 PCT/SE02/00070 -99and treated with about 4 equivalents (0.08 mmol) of PS-trisamine resin (primary amine PS resin) to scavenge any excess acylating or sulfonating reagent. The mixtures were sealed and stirred for 1.5 hours and then filtered directly into vials and concentrated to give the products.
The products were characterized by HPLC mass spectral analysis and were found to be greater than 90% pure by HPLC. The compounds were submitted to the 5-HT1b binding assay for determination of 5-HT receptor binding affinities and selectivities.
Example 44 0
N
0
N
C> N 0 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid propionyl-piperazin- 1 -yl)-phenyl]-amide.
This compound was prepared from 6-methoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid (4-piperazin-l -yl-phenyl)-amide (Example 43) and commercially available propionyl chloride (Aldrich) via the parallel synthesis described above. MS base peak at m/z =534 by positive ion CI Example 0.
00 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid [4-(4-ethane sulfonyl-piperazin-1-yl)-phenyl]-amide. MS base peak at m/z =570 by positive ion CI WO 02/055014 PCT/SE02/00070 100 This compound was prepared from 6-methoxy-8-(4-methyl-piperazin-l1-yl)-4-oxo-4flchromene-2-carboxylic acid (4-pip erazin-1 -yl-phenyl)-amide (Example 43) and commercially available ethanesulfonyl chloride (Aldrich) via the parallel synthesis described. above.
Example 46 0 o
N"N
N S N
U
6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-cbromene-2-carboxylic acid diehlsulfamoyl-piperazin- 1-yl)-phenyl]-amide.
This compound was prepared from 6-methoxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4Hchromene-2-carboxylic acid (4-piperazin- 1-yl-phenyl)-amide (Example 43) and commercially available dimethylsulfamoyl chloride (Aldrich) via the parallel synthesis described above. MS base peak at rnz =5 85 by positive ion CI Example 47 0 00 o N.
*00 4-[4-({l1-[6-Methoxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-chromen-2-yl] -methanoyl} amino)-phenyl]-piperazine-l1-carboxylic acid dimethylamide.
This compound was prepared from 6-methoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4Hchrornene-2-carboxylic acid (4-piperazin- 1-yl-phenyl)-amide (Example 43) and commercially available dimethylcarbamyl chloride (Aldrich) via the parallel synthesis described above. MIS base peak at mlz =549 by positive ion Cl WO 02/055014 PCT/SE02/00070 101 00 K- N 0N N 0 l-[6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromen-2-yl]-methanoyl)}amino)-phenyl]-piperazine- 1-carboxylic acid ethylamide.
This compound was prepared from 6-methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4Hchromene-2-carboxylic acid (4-pip erazin- 1 -yl-phenyl)-amide (Example 43) and commercially *available ethyl isocyanate (Aldrich) via the parallel synthesis described above.
MS base peak at m/z =549 by positive ion CL.
Example04 00 N 0N
N
<NN
I0 1 -[6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-cbromen-2-yl]-methanoy 1amnino)-phenyl]-piperazine- 1-carboxylic acid cyclohexylamide.
This compound was prepared from 6-methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4Hchroinene-2-carboxylic acid (4-piperazin-1 -yl-phenyl)-amide (Example 43) and commercially available cyclohexyl isocyanate (Aldrich) via the parallel synthesis described above. MS base peak at m/z =603 by positive ion Cl WO 02/055014 WO 02/55014PCT/SE02/00070 -102- Example I-[6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromen-2-yl]-methanoyl}amino)-plienyl]-piperazine-1 -carboxylic acid cyclopentylamide.
This compound was prepared from 6-metlioxy-g-(4-methyl-piperazin-l -yl)-4-oxo0-4Hchromene-2-carboxylic acid (4-piperazin-lI -yl-phenyl)-amide (Example 43) and commercially available cyclopentanecarbonyl chloride (Aldrich) via the parallel synthesis described above.
MS base peak at m/z =574 by positive ion CL.
Example 51 6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid pyrrolidin- 1 -yl-me thanoyl)-piperazin- 1 -yl] -phenyl) -amide.
This compound was prepared from 6-methoxy-8--(4-methyl-piperazin- I -yl)--4-oxo-4Hchromene-2-carboxylic acid (4-pip erazin-l1 -yl-phenyl)-amide (Example 43) and commnercially available 1 -pyrrolidinecarbonyl chloride (Aldrich) via the parallel synthesis described above.
MS base peak at nilz =575 by positive ion CL.
WO 02/055014 PCT/SE02/00070 103 Example 52 0 0N
N-
0 N 0 0 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid f{4-[4- (propane-2-sulfonyl)-piperazin- 1-ylj-phenyl }-amnide.
This compound was prepared from 6-methoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid (4-piperazin-1 -yl-phenyl)-amide (Example 43) and commercially available isopropylsulfonylonyl chloride (Aldrich) via the parallel synthesis described above.
MS base peak at m/z =584 by positive ion CL.
Example 53 0
NN
0 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid f methyl-propanoyl)-piperazin- 1-yl]-phenyl}-amide. This compound was prepared from 6-methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-411chromene-2-carboxylic acid (4-piperazin-lI -yl-phenlyl)-amide (Example 43) and commercially available isobutyryl chloride (Aldrich) via the parallel synthesis described above. MS base peak at m/z =548 by positive ion C1.
WO 02/055014 WO 02/55014PCT/SE02/00070 104 Example 54 6-Methoxy-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chromene-2-carboxylic acid 1moipholin-4-yl-methanoyl)-piperazin-l1 yl]-phenyl}-amnide.
This compound was prepared from 6-methoxy-8.-(4-methyl-piperazin-l -yl)-4-oxo-4Hcbromene-2-carboxylic acid (4-piperazin- 1 -yl-phenyl)-amide (Example 43) and commercially available morpholine-4-carbonyl chloride (Aldrich) via the parallel synthesis described above.
MS base peak at mlz =5 91 by positive ion Cf.
Example 6-Fluoro-8--(4-methyl-piperazin- I -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin-4yl-phenyl)-amide.
This compound was prepared from 6-Fluoro-g-(4-methyl-piperazin- I -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 3) and 4-morpholin-4-ylphenylarnine (Reference Example 20) as prepared in Example 1, yielding a yellow solid. MS (M-IH) m/z 467 WO 02/055014 PCT/SE02/00070 -105- Example 56
F
N
N
N S 1N 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid methanesulfonyl-piperazin-1 -yl)-phenyl]-amide.
This compound was prepared from 6-Fluoro-8-(4-methyl..piperazin- 1 -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 3) and 4-(4-methanesulfonylpiperazin- I -yl)-phenyl amine (Reference Example 12) as prepared in Example 1, yielding a yellow solid. MS m/z =544 Example 57 0
F
N
NN
oo -0 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-ck-romene-2-carboxylic acid [4-(4-acetylpiperazin- 1 -yl)-phenyl]-amide.
This compound was prepared from 6-Fluoro-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 3) and 1-[4-(4-amninophenyl)-piperazin- 1-yl]-ethanone (Reference Example 11) as prepared in Example 1, yielding a yellow solid. MS mlz 508 WO 02/055014 PCT/SE02/00070 106 Example 58 0
F
C1 0 N 0 K) N 6-Fluoro-8-(4-methiyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid (3-chlorov-4morpholin-4-y1-phenyl)-amide.
6-Fluoro-8 -(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride (Reference Example 3) (150 mg, 0.43 mmol), 1-hydroxybenzotriazole (140 mg, 0.9 minol), 1H-Benzotriazol- 1-yl)-N,N,N',N'-pentamethylene-uronium tetrafluoroborate (290 mg, 0.9 mmol), 4-(dirnethylam-ino)pyridine (10 mng, catalytic), triethylamine (0.2 mnL, 1.5 mmol), and commercially available 3-chloro-4-morpholin-4-ylphenylamine (Maybridge) were dissolved in dimethylformamide (2.5 mL) and stirred at room temperature overnight. At 17 h, water (20 mL) was added and the resulting mixture was stirred for 15-30 min. The mixture was vacuum-filtered and the residue washed with water and air-dried to yield a yellow powder (220 mg =quantitative yield). LC/MS mlz 501.5 Example 59 0
F
0N
N)
6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (3-fluoro-4morpholin-4-yl-phenyl)-amide.
This compound was prepared from 6-Fluoro-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4Hchroinene-2-carboxylic acid hydrochloride (Reference Example 3) and 3-fluoro-4-morpholin- 4-yl-phenylamine (Reference Example 16) as prepared in Example 58, yielding a yellow solid (210mig LC/MS m/z 485.5 WO 02/055014 PCT/SE02/00070 -107- 0
F
N
N
0 N
N
6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (3-cyano-4morpholin-4-yl-phenyl)-amide.
This compound was prepared from 6-Fluoro-8-(4-methyl-piperazin. I -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 3) and 5-amino-2-morpholin- 4-yl-benzonitrile (Reference Example 15) as prepared in Example 58, yielding a yellow solid (210 mg LC/MS niiz =492.5 Example 61 0
F
N0 00
QN
101 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid [4-(1Imorpholin-4-yl-methanoyl)-phenyl]-amide.
This compound was prepared from 6-Fluoro-8-(4-methyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 3) and 1 -(4-amino-phenyl)- 1 morpholin-4-yl-methanone (Reference Example 14) as prepared in Example 58, yielding a yellow solid (220 mg quantitative yield). LC/MS m/z 495.5 Example 62 WO 02/055014 PCT/SE02/00070 108 6-Methyl-8-(4-methyl-piperazin- 1-yl)-4-oxo-411-chromene-2-carboxylic acid (4-morpholin-4yl-phenyl)-amide.
This compound was prepared from 6-Methyl-8-(4-methyl-piperazin-l -yl)-4-oxo-4Hcbromene-2-carboxylic acid hydrochloride (Reference Example 4) and 4-morpholin-4-ylphenylamine (Reference Example 20) as prepared in Example 1, yielding a yellow solid.
LCMS nih 463.6 0 K- N 0 0o 0 I
_N,
CN0 6-Methyl-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-ch-romene-2-earboxylic acid [4-(l1morpholin-4-yl-methanoyl)-phenyl]-amide.
This compound was prepared -from 6-Methyl-8-(4-methyl-piperazin-1 -yl)-4-oxo-4Hc hromene-2-carboxylic acid hydrochloride (Reference Example 4) and 1 -(4-amino-phenyl)- 1 morpholin-4-yl-methanone (Reference Example 14) as prepared in Example 1, yielding a yellow solid. LCMS mlz 491.6 Example 64 0
H
3
C
N F 0 N0 0 6-Methyl-8-(4-methyl-piperazin- 1-yl)-4-oxo-411-chromene-2-carboxylic acid (3-fluoro-4morpholin-4-yl-phenyl)-amide.
This compound was prepared from 6-Methyl-8-(4-methyl-pipera'zin-l -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 4) and 3-fluoro-4-morpholi-n- WO 02/055014 PCT/SE02/00070 -109- 4-yl-phenylamine (Reference Example 16) as prepared in Example 1, yielding a yellow solid.
LCMS -rn/z=504.5 Example 0
CI
N
0 0 6-Chloro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin-4yl-phenyl)-amide.
This compound was prepared from 6-chloro-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 5) and 4-morpholin-4-ylphenylamine (Reference Example 20) as prepared in Example 1, yielding a yellow solid.
LCMS-mlz=483.3 Example 66
OH
3 0
NN
00
NN
5-Methyl-8-(4-methyl-piperazin- l-yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin-4yl-phenyl)-amide.
This compound was preparcd from 5-mcthyl-8-(4-methyl-piperazin-l -yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 6) and 4-morpholin-4-ylphenylamine (Reference Example 20) as prepared in Example 1, yielding a yellow solid (116 mg 84%) LCMS- m/z 463.5 WO 02/055014 PCT/SE02/00070 -110- Example 67
N
0 0 0 N 0
NN
5-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin- 4-yl-phenyl)-amide.
This compound was prepared from 5-methoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 7) and 4-morpholin-4-ylphenylamine (Reference example 20) as prepared in Example 1, yielding a yellow solid (149 mg 50%) LCMS nt/z =479.4 The following additional examples incorporate 4-substituted piperazine-1I-yl-phenyl amides similar in structure to Examples 44-54 Example 68 0 0 N 0 0 N <N N OH 0 6-Mcthoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromcne-2-carboxylic acid hydroxy-propanoyl)-piperazin-1 -yl]-phenyl} -amaide.
6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-cbromene-2-carboxylic acid (4piperazin-lI-yl-phenyl)-amide (Example 43) (1.5 gram, 2.12 mmol) was placed in a 100 naL flask with 50 mL of CH 2 C1 2 This suspension was treated with triethylamine (4 equivalents, 1.2 mL, 8.5 namol) and -propionylactone (0.2 mL, 3.2 nimol) and the reaction stirred at room temperature for 2 hours, then heated to 50'C for 2 hours. Then 0.8 ml more of bpropionylactone was added and the reaction heated for 4 hours more. The reaction was WO 02/055014 PCT/SE02/00070 allowed to cool to room temperature and then concentrated (1 mm Hg pressure). The concentrate was treated with saturated aqueous sodium bicarbonate and the resulting solid collected by vacuum filtration. The residue was purified by chromatography on silica eluting -with 2% methanol in chloroform, then concentrated (1mm Hg pressure). Then triturated with either to yield a yellow, powder with was dried under high vacuum for 48 h at 50"C (100 mg) LCMS mi/z 550, mp 195-197C.
,Example 69 0
F
0% Na N Y ON K N 0 1 -[6-Fluoro-8-(4-mothyl-piperazin- 1 -yl)--4-oxo-4H-cliromen-2-yl]-methanoy }-amino)phenyl]-piperazine-l1-carboxylic acid tert-butyl ester.
This compound was prepared from 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4Hchromene-2-carboxylic acid hydrochloride (Reference Example 3) and 4 -(4-Amino-phenyl)piperazine- 1 -carboxylic acid tert-butyl ester (Reference Example 17) according to the method of Example 42 to yield (1.65 grams, 64%) of a yellow powder LCMS m/z =556; rap 219-220 0
C.
Example 0
F
0%Nj CN 0
N
NH
N
1 -[6-Fluoro-8-(4-miethyl-piperazin-1 -yl)-4-oxo-4H-cliromene-2-carboxylic acid (4piperazin- 1 -yl-phenyl)-amide.
This compound was prepared from {11-[6-Fluoro-8-(4-methyl-piperazin- 1 -yl)-4oxo-4H-chromen-2-yl]-methanoyl} -amino)-phenyl]-piperazine-l1-carboxylic acid tert-butyl WO 02/055014 PCT/SE02/00070 112 ester, as prepared in Example 69, using the method of Example 43 to yield a yellow solid LCMS mz =466.
Example 71 0
F
0
N
0 0 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid [4-(4-ethane sulfoniyl-piperazin-l -yl)-phenyl]-amide.
1 -[6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromnene-2-carboxylic acid (4-piperazin- 1 -yl-phenyl)-amide ditrifluoroacetate (the free acid of which was prepared as in Example 70) (4.0 grams, 5.77 mmol) was placed in a flask with 50 mL of CH 2 Cl 2 and triethylamine (3.2 mL and 23 mmol) and ethylsulfonyl chloride was added (0.6 mL, 6.35 mmol) portionwise 1 mL at a time) over' 15 minutes and allowed to stir at room temperature for 20 hours. The reaction was concentrated (1 mim Hg pressure) and then saturated aqueous sodium bicarbonate was added and extracted with CHCI 3 The organic fractions were combined, washed with saturated sodium chloride, dried (MgSO 4 concentrated (1 mm Hg pressure) to give a yellow solid which was recrystallized from methanol to give 1.33 grams of product LCMS ni/z 558, mp =233-234 0
C.
Example 72 0
F
N
N
N
NN
0 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid [4-(4-propionylpiperazin- 1-yl)-phenyll -amide.
[6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4-piperazin- 1 -yl-phenyl)-amide ditrifluoroacetate (the free acid of which was prepared as in WO 02/055014 PCT/SE02/00070 113 Example 70) (0.69 grams, 1,00 mnmol) was placed in a flask with 25 mL of C11 2 0 2 and triethylarnine (0.56 mL and 4 mmol) and propionyl chloride was added (0.95 mL, 1. 1 mmol) and the reaction allowed to stir at room temperature for 20 hours. The residue was purified by chromatography on silica Oluting with 2% methanol in chloroform, then concentrated (1 mm Hg pressure). The residue was triturated with either then digested with CHC1 3 and the CHC1 3 concentrated to yield a yellow powder which was dried under high vacuum for 48 h at (260 mg) LCMS m/z =522.
Example 73 0
F
N
N
N
0 N OH 1 0 6-Fluoro-8-.(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid hydroxy-propanoyl)-piperazin- -yl]-phenyl}-amide.
This compound was prepared from 6-Fluoro-8-(4-methyl-piperazin- 1-yl)-4-oxo-4Hchromene-2-carboxylic acid (4-piperazin-1I -yl-phenyl)-amide and f3-propionylactone using the method described above in Example 68 to yield 65 mg of a yellow powder LCMS m/z= 538, mp 195-199'C.
The following exemplifies a. substituted chromene-2-"reverse amide" (or substituted chromene-2-yl-benzamide).
Example 74 0 N. 0 O0
N
N
N-[S-(4-Methyl-piperazin- 1 -yl)-4-oxo-4H-chromen-2-yl]-4-morpholin-4-yl-benzamide.
8-(4-Methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid hydrochloride Reference Example 1 (227 mg, 0.69 mmol), triethylamine (2 equivalents, 1.389 mmol, 0. 193 WO 02/055014 PCT/SE02/00070 -114mL) and diphenylphosphoryl azide (0.69 mmol, 0.15 mL) were stirred in toluene (10 mL) at for 30 minutes. The reaction was allowed to cool to 22°C and 4-morpholinobenzonoic acid (0.7 mmol, 145 mg), more triethylamine (0.051 mL, 0.7mmol), and CH 3 CN (5 mL) were added and the reaction heated to reflux for 1 hour. The reaction was concentrated (1 mm Hg pressure) the residue was partitioned between 1N methanesufonic acid and ether. The acid layer was then basified with solid K 2 CO3 and the product extracted in to CHC13. The organic layer was dried (MgSO 4 and concentrated under reduced pressure to leave a yellow solid which was further purified with silica chromatography using CHC1 3 to 4% CH 3 OH in CHCl 3 Concentration of the fractions containing product yielded 13 mg of product LC/MS m/z 449.
Enantiomers of 8-(4-Methyl-piperazin-1-yl)-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
Example
N
O
N
racemic-8-(4-Methyl-piperazin-1-yl)-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)amide.
racemic-8-(4-Methyl- 1-piperazin-l -yl)-chroman-2-carboxylic acid hydrochloride (Example 75a) (1.04 mmol) was dissolved in anhydrous N,N-dimethylformamide (40 ml) and the following were added in order: HOBt (0.17 g, 1.14 mmol), TBTU (0.37 g, 1.14 mmol) then triethylamine (0.6 ml, 4.2 mmol). After stirring for 5 min at room temperature, 4-(4morpholinyl)aniline (reference example 20) (0.185 g, 1.14 mmol) was added and the reaction stirred overnight at room temperature.
The solution was concentrated in vacuo, the remains were partitioned between chloroform saturated sodium bicarbonate, extracted (x3) with chloroform, dried (MgSO 4 and concentrated in vaczo to give the crude product.
The crude product was chromatographed on a Waters Delta Prep 4000 using 1 PrepPak cartridge (Porasil 37-55pm 125A) eluting with 2.5 methanol chloroform. The product was collected to give a yellow oil. Ethyl acetate was added to the oil. The solution was WO 02/055014 PCT/SE02/00070 -115refluxed then cooled the yellow solid was filtered to give 55 mg (12% yield) ofracemic-8-(4methyl-piperazin- 1-yl)-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (mp 215-216 OC). The mother liquor contained 76 mg that was used in the chiral separation described below. LC/MS m/z 437.
Example racemic-8-(4-Methyl- -piperazin-1-yl)-chroman-2-carboxylic acid hydrochloride.
Ethyl 8-(4-methyl-1 -piperazin-1 -yl)-4-oxo-4H-chromen-2-carboxylate (Reference Example 1) (0.74 g, 2.3 mmol) was dissolved in glacial acetic acid (50 ml) and 10 palladium on carbon (80 mg) was added. The mixture was hydrogenated on a Paar apparatus (50 psi) at 70 'C for 3 h. Then, concentrated HC1 and 10 palladium on carbon (100 mg) were added and the mixture was again subjected to hydrogenation (50 psi) at 70 °C for lh.
The reaction was allowed to cool, the catalyst was filtered and the solution was concentrated in vacuo. Toluene was repeatedly added and the solution concentrated to give racemic-8-(4- Methyl-1-piperazin- 1-yl)-chroman-2-carboxylic acid hydrochloride as a foam that was used without further purification in the next reaction. LC/MS m/z 277.
Example 76
N
0 N 0 (+)-8-(4-Methyl-piperazin- 1 -yl)-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)amide.
The enantiomers of racemic-8-(4-Methyl-piperazin-1-yl)-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (Example 75) (0.52 g, 1.19 mmol) were separated by the use of a chiral column (ChiralPak AD, 5 cm X 50 cm, 20 The faster isomer (example 76) was eluted with 45 isopropanol hexane and the slower (-)isomer (example 77) was eluted with 75 isopropanol hexane.
The faster isomer (example 76) was obtained as a white solid (250 mg, mp 206- 207 aD 92.66 in dichloromethane). LC/MS m/z 437.
WO 02/055014 PCT/SE02/00070 -116- Example 77
N
0 N 0 (---(-ety-iprzi N~ N 0 (-)8-(-Mehylpiprazn--yl)-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
The enantiomers of racemic-8-(4-Methyl-piperazin- 1 -yl)-chrornan-2-carboxylic acid (4-miorpholin-4-yl-phenyl)-ainide (Example 75) (0.52 g, 1.19 mmol) were separated by the use of a chiral colun (ChiralPak AD, 5 cm X 50 cm, 20 The faster isomer (example 76) was eluted with 45 isopropanol hexane and the slower (-)isomer (example 77) was eluted-with 75 isopropanol hexane.
The slower isomer (example 77) was obtained as obtained as a light purple solid (260 mg, mp 205.5-207 0 C, cD 91.08 in dichioromethane). LC/MS (MI-i) m/z 437.
Enantiomers of 8-(4-methyl-piperazin- 1-yl)-4-oxo-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amicle.
Example 78 0
N
*0 C -N N0
NN
racemic-8-(4-methyl-piperazin- 1-yl)-4-oxo-chroman-2-carboxylic acid (4-morpholin-4-ylphenyl)-amide.
Racemic-8-(4-methyl-l1-piperazin- l-yl)- 4-oxo-chroman-2-carboxylic acid hydrochloride (Example 78a) (1.04 mmol) was dissolved in anhydrous NNdimethylformamide (40 ml) -and the following were added in order: HOBt 17 g, 1. 14 mmol), TBTU (0.37 g, 1. 14 mmol) then triethylamine (0.6 ml, 4.2 mmol). After stirring for min at room temperature, 4-(4-morpholinyl)aniline (reference example 20) (0.185 g, 1. 14 mmol) was added and the reaction stirred overnight at room temperature.
WO 02/055014 PCT/SE02/00070 -117- The solution was concentrated in vacuo, the remains were partitioned between chloroform saturated sodium bicarbonate, extracted (x3) with chloroform, dried (MgSO 4 and concentrated in vacuo to give the crude product.
The crude product was chromatographed on a Waters Delta Prep 4000 using 1 PrepPak cartridge (Porasil 37-55gm 125A) eluting with 2.5 methanol chloroform. The product was collected to give a yellow oil. Ethyl acetate was added to the oil. The solution was refluxed then cooled the yellow solid was filtered to give 55 mg (12% yield) of racemic- 8-(4-methyl-piperazin- 1 -yl)-4-oxo-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)amide (mp 215-216 OC). The mother liquor contained 76 mg that was used in the chiral separation described below. LC/MS m/z 451.
Example 78a racemic-8-(4-Methyl- 1-piperazin-1l-yl)- 4-oxo-chroman-2-carboxylic acid hydrochloride.
racemic-Ethyl-8-(4-methyl- 1-piperazinyl)- 4-oxo-chroman-2-carboxylate (Example 78b) (0.33 g, 1.04 mmol) was dissolved in 6 M HCI (20 ml) and heated to 100 "C for 1.5 h.
The reaction was allowed to cool. The solution was concentrated in vacuo and anhydrous toluene was added (x3) and the solution was again concentrated in vacuo to give racemic-8- (4-Methyl-1 -piperazin- 1 4-oxo-chroman-2-carboxylic acid hydrochloride as a yellow foam (0.44 g, quantitative yield) that was used as is in the next reaction. LC/MS m/z 291.
Example 78b racemic-Ethyl-8-(4-methyl- 1 -piperazin- I 4'oxo-chroman-2-carboxylate.
Racemic-Ethyl-8-(4-methyl- 1 -piperazin- 1 -yl)-4-hydroxy-chroman-2-carboxylate (Example 78c) (0.43 g, 1.3 mmol) was dissolve in anhydrous dichloromethane (35 ml) and manganese dioxide (1.2 g, 13 mmol) was added. The reaction stirred at room temperature overnight.
The reaction was filtered through diatomaceous earth and the solvent was removed in vacuo to give racemic-Ethyl-8-(4-methyl- 1-piperazin-1-yl)- 4-oxo-chroman-2-carboxylate as a white solid (0.37 g, 86 yield) that was used as is in the next reaction. GC/MS (EI, M+) rm/z 318.
Example 78c racemic-Ethyl-8-(4-methyl- 1 -piperazin- l-yl)- 4-hydroxy-chroman-2-carboxylate.
Ethyl 8-(4-methyl-1 -piperazin-1-yl)-4-oxo-4H-chroman-2-carboxylate (reference example 1) (0.48 g, 1.5 mmol) was dissolved in glacial acetic acid (50 ml) and 10 WO 02/055014 PCT/SE02/00070 palladium on carbon (100 mg) was added. The mixture was hydrogenated on a Paar apparatus psi) at 70 'C for 3 h.
The reaction was allowed to cool, the catalyst was filtered and the solution was concentrated in vacuo. Ethyl acetate saturated sodium bicarbonate was added to the remains and the mixture was extracted (x3) with ethyl acetate, dried (MgS 04) and stripped to give racernic-Ethyl-8-(4-methyl- I piperazin- Il-yl)- 4-hydroxy-chroman-2-carboxylate (0.43 g, yield) as a yellow oil. GC/MS (El, rn/z =320.
Example 79 0.
N
0 CN 0N N 0N 8-(4-Methyl-piperazin- 1 -y)-4-oxo-chroman-2-carboxylic acid (4-morphlin-4-yl-phenyl)amide (faster running isomer).
The enantiomers of the racemic-8 -(4-methyl-piperazin- 1-yl)-4-oxo-chroman-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide (Example 78) (100 mg, 0.22 mmol) were separated by the use of a chiral column (ChiralPak AD, 5 cm X 50 cm, 20 The isomers were eluted with a gradient of 35-55 isopropanol hexane. The faster isomer was obtained as a light yellow solid (40 mg, rap 216 TC dec.) LC/MS m/z =45 1.
01
N
0% QN 0 N4 8-(4-Methyl-piperazin- 1-yl)-4-oxo-chroman-2-carboxylic acid (4-morpholin-4-yl-phenyl)amide (slower running isomer).
The enantiomers of the racemic-8-(4-methyl-piperazin- 1-yl)-4-oxo-chroman-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide(1 00 mg, 0.22 mmol) were separated by the use of a chiral colun (ChiralPak AD, 5 cm X 50 cm, 20 The isomers were eluted with a WO 02/055014 PCT/SE02/00070 gradient of 35-55 isopropanol hexane. The slower isomer was obtained as an off white solid (32 mg,rmp 215 0 C dec.) LC/IvIS i/z =451.
Example 81 0
F
N
0 N> 0 [6-Fluoro-8-(4-methayl-piperazin- 1 -yl)-4-oxo-4H-chromen-2-y] -methanoyl }-amino)phenyl]-piperazine- 1-carboxylic acid ethylamide: 6-Fluoro-8-(4-methyl-piperazin- 1 -yl)-4-oxo-4H-chiromene-2-carboxylic acid (4-piperazin-1 yl-phenyl)-amide (Example 71) (150 mg, 0.216 mmnol) was placed in a 50 niL flask with mL of CH2Cl2. This suspension was treated with triethylamine 1 mL, 0.67 mmol) and ethylisocyanate (0.21 mL, 1 8.7 ing, 0.26 mmol) and the reaction stirred at roomn temperature for 18 hours. The reaction was concentrated (1 mm Hg pressure) and the concentrate purified by chromatography on silica eluting with 1% methanol in chloroform, then concentrated (1mm Hg pressure). Then triturated with either to yield a yellow powder with was dried under high vacuum for 48. h at 50'C (79 mg) LCMS AP+ 537.4, mnp 236-238'C.
Example 82 0 0
NN
6-Methoxy-8-(4-methyl-[ 1,4]diazepan- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide: Into a 100 mL round bottom flask equipped with a nitrogen inlet and magnetic stirrer is added 327 mng (0.89 mmol, 1.0 equiv.) of 6-Methoxy-8-(4-methyl-[1,4]diazepan-l-yl)-4oxo-4H-chromene-2-carboxyhic acid hydrochloride salt (Reference Example 23). This WO 02/055014 PCT/SE02/00070 -120material is dissolved in 20 mL of DMF and then 189 mg (1.06 mmol, 1.2 equiv.) of 4morpholinoaniline is added. To the stirred solution is quickly added simultaneously added 568 mg (1.77 mmol, 2.0 equiv.) of TBTU and 239 mg (1.77 mmol, 2.0 equiv.) of HOBT. At this point 457 mg, 577 gL (25.2 mmol, 4.0 equiv.) is added via syringe over 5 minutes. The reaction is allowed to stir at room temperature for 18 hrs, then is concentrated on a rotary evaporator under high vacuum in order to remove the DMF. The residue is triturated with methanol and the crude solids are recovered by filtration. These residues are then purified by flash chromatography using a gradient of 5-10% methanol in methylene chloride as eluent.
The eluted material, which is obtained from chromatography, is concentrated, dried under high vacuum, suspended in methylene chloride, dried over K 2 C0 3 concentrated, then crystallized from methanol to give the free base of the pure product as 345 mg of a yellow solid. Mass Spec.: calc. for [C 27
H
3 2
FN
4 05+H] Theor. m/z 393; Obs. 393 Example 83 0
N,
ON
0 6-Ethoxy-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin-4yl-phenyl)-amide: Into a 100 mL flask equipped with a nitrogen inlet and magnetic stirrer is placed 133 mg (.748 mmol, 1.1 equiv.) of 4-morpholinoaniline, which is then dissolved in 20 mL of methylene chloride. To this mixture is then added 290 mg, 367 gL (2.24 mmol, 3.3 equiv.) of ethyldiisopropyl amine, followed by addition of a solution of 250 mg (0.68 mmol, 1.0 equiv.) of 6-ethoxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carbonyl chloride (Reference Example 23) which has been dissolved in 10 ml of methylene chloride. The reaction is allowed to stir for 4 hr, after which no further formation of product was seen by LC/MS. The crude reaction was concentrated on a rotary evaporator, then triturated with 10 mL of methanol. The crude solids were collected by filtration, then subjected to flash chromatography using a gradient of from 2 to 20% methanol in methylene chloride.
WO 02/055014 PCT/SE02/00070 121 Recrystallization. from methylene chloride and hexanes afforded 55 mg of the pure product as a yellow solid.
Mass Spec.: caic. for [C 2 7
H
3 2
N
4
O
5 Theor. mnlz 493; Obs. =493 Example 84 0 K N o N 0N
N
0 6-Ethoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-4H-chromene-2-carboxylic acid [4-(4-propionylpip erazin- 1 -yl) -phenyl] -amide: This compound was prepared from 250 mg (0.68 minol, 1.0 equiv.) of 6-Ethoxy-8-(4methyl-piperazin- 1 -yl)-4-oxo-4H-cbromene-2-carbonyl chloride (Reference Example 23) and 175 mg (0.748 mmol, 1. 1 equiv.) of 1-[4-(4-Amino-phenyl)-piperazin-1 -Yl]-ptopan-1 -one by an analogous procedure to that used to prepare the 4-morpholino aniline derivative, to give mg of the desired product as a yellow solid.
Mass Spec.: caic. for [C 3 oH 3 7N 5
O
5 Theor. m/z =548; Obs. =548 Example 0 Ao
N
CNN
N
6-Methoxy-4-oxo-8-piperazin- 1 -yl-4H-chrornene-2-carboxylic acid (4-morpholin-4-ylphenyl)-amide: Into a 5 0 mL round bottom flask equipped with a reflux condenser, nitrogen inlet and magnetic stirrer is placed 50 mg 115 mmol, 1.0 equiv.) of 6-Methoxy-8-(4-methylpiperazin- 1-yl)-4-oxo-4H-chr-omene-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (Example 3 1) and 10 mL of 1, 2 dichloroethane. To this solution is then added via syringe 49 -mg, 37 [tL (0.345 mmol, 3.0 equiv.) of 1-chloroethyl chloroformate. A precipitate forms, WO 02/055014 PCT/SE02/00070 -122indicating formation of an intermediate. The reaction is heated to reflux for 3 days, whereupon an analysis of an aliquot by LC/MS indicates only a trace of product has formed.
At this time 52 mg (0.345 mmol, 3.0 equiv.) of sodium iodide are added to the refluxing reaction. LC/MS analyses then progressively show formation of demethylated product over additional days. The reaction is then cooled, concentrated on a rotary evaporator, then dried over K 2 C0 3 as a suspension in methylene chloride containing methanol, removal of solids by filtration, followed by flash chromatography of the solution, using a gradient of 5 to methanol in methylene chloride, gives 34 mg of the pure product as a reddish solid.
Mass Spec.: calc. for [C 25
H
2 8N 4 Os+H] Theor. m/z 465; Obs. 465 Example 86
O
0 N 0
NN
6-Hydroxy-8-(4-methyl-piperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin- 4-yl-phenyl)-amide: Into a 50 mL round bottom flask equipped with a reflux condenser, nitrogen inlet and magnetic stirrer is placed 50 mg (0.115 mmol, 1.0 equiv.) of 6-Methoxy-8-(4-methylpiperazin-1 -yl)-4-oxo-4H-chromene-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (Example 31) and 20 mL of methylene chloride. To this solution is added 1 mL of a 1N solution of boron tribromide in methylene chloride. The reaction is stirred at room temperature for 2.5 days at which time it is complete by LC/MS. The reaction is concentrated on a rotary evaporator, then methanol is added. The methanol is concentrated and readded times, until the BBr 3 is removed as HBr and trimethyl borate. The solid hydrobromide salt residue, which is obtained, is >85% pure product by LC/MS. Mass Spec.: calc. for
[C
25
H
2 sN 4 05+H] Theor. m/z 465; obs. 465 WO 02/055014 PCT/SE02/00070 123 Example 87 (Method 1) 0 N
N
N H
N
6-Methoxy-8-(4-methyl-[ 1,4] diazepan- 1-yl)-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
To a solution of 6-metlioxy-8 -(4-methyl-[1 ,4]diazepan- 1-yl)-4-oxo. I,4-dihydroquinoline-2-carboxylic acid 10 mmol) (Reference Example 25b) and diisopropylethyl amine (1.4 mL, 8.6 rnmol) 11134 mL dimethylformamide was added TBTU (1.40 g, 4.36 mmol) and HOBt 58 8 g, 4.3 5 mmol) followed by the addition of 4-morpholinoaniline (0,463 g, 2.60 mmol). The resulting dark brown solution was stirred' at room temperature under nitrogen for 19 hours. The reaction was concentrated in vacuo and the resulting crude product was taken up in mathylene chloride/methanol. Filtration of the resulting mixture afforded some product as a yellow solid. The filtrates were concentrated and partitioned between methylene chloride and saturated aqueous sodium bicarbonate. The organic layer was washed with saturated sodiuLm bicarbonate, dried (MgSO4), and concentrated under vacuum to afford a brown solid. This was suspended in methanol and filtered to afford the desired product as a yellow solid (0.7 14 g,1 'H NMR (300 MHz, DMSO, 8 9.97 (bs, 1 H, NUl), 7.67 2 H, 4= 8.8 Hz, ArH 2 HO', 7.47 (bs, 1 H, Arij 5 7.00 I H, C=Cf), 6.99 2 H, 8.8 Hz, ArHy,& HO', 6.71 (bs, 1 H, ArH 7 3.85 3 H, 0CH 3 3.75 4 H, J= 4.6 Hz, OCHimCH 2 3.70 (bs, 2 H, ArNCHCH 2
CH
2
NCH
3 3.55 (bs, 2 H, ArNCH? 2
CH
2
NCH
3 3.09 4 H, .k 4.6 Hz, OCH 2
CII
2 2.95 (bs, 2 H, ArNCH 2 Cli7NCHA) 2.73 (bs, 2 H, ArNCH 2
CH
2 Cli 2
NCH
3 2.36 3 H, Nd 3 2.07 (bs, 2 H ArNC-H 2 Cfl 2
CH
2
NCH
3 Mass Spec.: calc. for [C 27
H
33
N
5
O
4 Theor. m/z 492; Obs.
492.
WO 02/055014 PCT/SE02/00070 -124- Example 87 (Method 2) 0
I
NYN
NN
H 0 6-Methoxy-8-(4-methyl-[ 1,4] diazepan- 1-yl)-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
A solution of 6-methoxy-8-(4-methyl-[ 1,4]diazepan- 1-yl)-4-(2-trimnethylsilanyl.
ethoxymethoxy)-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amide (Reference Example 27d) (0.989 g, 1.59 rnrnol) in 20 nl, methanol was poured into 300 mL 0.05 N hydrochloric acid. The clear dark yellow solution became cloudy within 5 minutes. The mixture was stirred at room temperature for 45 minutes and then adjusted to pH 7 with sodium hydroxide. The resulting yellow precipitate was isolated by filtration, washed with water, and dried under high vacuum to afford the desired product as a yellow solid (0.629 g, 'H NMR (3 00 MHz, DMSO, d 6 5 9.97 (bs, I H,C(O)NTJ), 7.67 2 H, J 0 8.8 Hz, Ar~H H 6 7.47 (bs, 1 H, ArHj5), 7.00 1 C=CIj, 6.99 2 H, J 0 8.8 Hz, ArH 3 6.71 (bs, 1 H, Ar H 7 .5(,3H C ,37 t ,J 4.6 Hz, OCH CH 2 3.70 (bs, 2 H, ArNCfiqCH 2
CH
2
NCH
3 3.55 (bs, 2 H, ArNCHlCH 2
NCH
3 3.09 4 H, J= 4.6 Hz,
OCH
2 Cfl2N), 2.95 (bs, 2 H, ArNCH 2
CH
2
NCH
3 2.73 (bs, 2 H, ArNCH 2
CH
2 Cjj2NCH 3 2.36 3 H, NC~H), 2.07 (bs, 2 H ArNCH 2 CH CH 2
NCH
3 Mass Spec.: caic. for
[C
2 7
H
33 NsO 4 Theor. m/z 492; Ohs. =492. Analysis for C 27
H
33
N
5 0 4 .l.OeqHCl.
0.3eqH 2 O: Calculated C 60.79 H 6.54 N 13,13. Found C 60.82 H 6.53 N 13.17.
Examiple 88 0 N yN N H 0 N 0 WO 02/055014 PCT/SE02/00070 -125- 6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo-1 ,4-dihydro-quinoline-2-carboxylic acid (4morpliolin-4-yl-phenyl)-aniide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method A yellow solid was obtained. Mass Spec.: caic. for [C 26
H
3 ,NsO 4 Theor. m/z =478; Obs.
478.
Example 89 0
H
N
N
N
N N 0 6-Methoxy-8-(4-methyl-piperazin- 1-yl)-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid propionyl-piperazin- 1 -yl)-phdnyl]-amidc.
The title compound was prepared from 8-bromno-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method except that the amide was formed from 1- [4-(4-amino-phenyl)-piperazin-lI -yl]-propan-1 -one. A yellow solid was obtained. Mass Spec.: caic. for [C 29 1H 36
N
6 0 4 Theor. mlz =533; Obs.
533.
Example 0 kN
N
N
0N 6-Fluoro-8 -(4-methyl-piperazin- 1-yl)-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide WO 02/055014 PCT/SE02/00070 -126- The title compound was prepared from 6-Fluoro-8-(4-methyl-piperazin-1-yl)-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid hydrochloride salt (Reference Example 26) using the procedure described in Example 87 (Method After chromatography, it is then crystallized from methanol to give the pure product as 150 mg of a yellow solid. Mass Spec.: calc.
for [C 25
H
28 FNs 5
O
3 Theor. m/z= 466; Obs. 466.
Example 91 0
F
N
NO
NN
0 6-Fluoro-8-(4-methyl-piperazin-1-yl)-4-oxo-1,4-dihydro-quinoline-2-carboxylic acid propionyl-piperazin- 1 -yl)-phenyl]-amide.
The title compound was prepared from 6-Fluoro-8-(4-methyl-piperazin-1-yl)-4-oxo- 1,4-dihydro-quinoline-2-carboxylic acid hydrochloride salt (200 mg, 0.59 mmol) (Reference Example 26) using the procedure described in Example 87 (Method 31% yield. Mass Spec.: calc. for [C 2
H
33
FN
6
O
3 Theor. m/z 521; Obs. 521.
Example 92 0
H
%N
N
NN
8-[(2-Dimethylamino-ethyl)-methyl-amino]-6-methoxy-4-oxo-1,4-dihydro-quinoline-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method WO 02/055014 PCT/SE02/00070 127 using N,N,N'-trimethy] ethylenediainine for the Pd catalysed coupling, A yellow solid was obtained. Mass Spec.: caic. for [C 26
H
33
N
5
O
4 Theor. mlz =480; Obs. =480.
Example 93 0
H
NN
~N H o 0
NN
-Dimethylamino-propyl) -methyl- amino] -6-methoxy-4-oxo- 1 ,4-dihydre-quinoline-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymnethoxy)-quinoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method using N,N,N '-trimethyl- 1,3 -propanediamine for the Pd catalysed coupling. A yellow solid was obtained. Mass Spec.: caic. for FC 27
H
35
N
5
O
4 Theor. m/.z 494; Obs. =494.
Example 94 0 N H o
NN
-NN
-Dimethylan-jino-pyrrolidin -1 -yl)-6-rnethoxy-4-oxo- 1,4-dihydro-quinoline-2carboxylic acid (4rmorpholin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quinoline-2-carboxylic acid methyl (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method using (3R)-(+)-3-(dimethylamino)pyrrolidine for the Pd catalysed coupling. A yellow solid was obtained. Mass Spec.: calc, for [C 27
H
33
N
5 0 4 Theor. m/z 492; Obs. 492.
WO 02/055014 PCT/SE02/00070 128 Example 0 00
-NN
-Dimnethylarnin-o-pyrrolidin -1 -yl)-6-rnethoxy-4-oxo- 1,4-dihydro-quinoline-2carboxylic acid (4-morpholiin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-q-Linoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method using (3S)-(-)-3-(dirnethylamino)pyrrolidiuie for the Pd catalysed coupling. A yellow solid was obtained. Mass Spec.: caic. for [C 27 I1 33
N
5
O
4 Theor. m/z 492; Obs. =492.
Example 96 0 N N
N
N H a 0
N
6-Methoxy-8- [methyl-(l1-methyl-pyrrolidin-3 -yl)-amino]-4-oxo- 1,4-dihydro-quinoline-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxymethoxy)-quiinoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method using N,N'-dimethiyl-3-amninopyrrolidine for the Pd catalysed coupling. A yellow solid was obtained. Mass Spec.: calc, for [C 27 Ii 33
N
5 0 4 Theor. ni/z =492; Obs. 492.
WO 02/055014 PCT/SE02/00070 129 Example 97 0 N H
NN
0
N
8-[Ethyl-( 1 -ethyl-pyrrolidin-3 -yl) -amnino] -6-methoxy-4-oxo- 1 ,4-dihydro-quinoline-2carboxylic acid (4-morpholin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bromo-6-methoxy-4-(2-trimethylsilanylethoxyinethoxy)-quiinoline-2-carboxylic acid methyl ester (Reference Example 24c) according to the procedures described in Reference Example 25a and in Example 87 (Method using 3-diethylamninopyrrolidine for the Pd catalyzed coupling. A yellow solid was obtained. Mass Spec.: caic. for [C 29
H
37
N
5
O
4 Theor. mlz 520; Obs. =520.
Example 98
N
N
N
No "a N
N
4-Dimethylamino-6-methoxy-8 -(4-methyl-piperazin- 1-yl)-quinoline-2-carboxylic acid (4morpholin-4-yl-phenyl)-arnide.
To a suspension of 8-brorno-4-dimethylamino-6-methoxy-quinoline-2-carboxylic acid (4-morpholin-4-yl-phenyl)-amiide (Reference Example 28b) (139.9 mg, 0.288 nunol), Nmethylpiperazine (48 0.43 mmol), and 4 A sieves in 15 mL anhydrous toluene was added Pd 2 (dba) 2 (15.3 mg, 16.7 pitol), BINAP (63.0 mg, 0.101 mmol) and cesium carbonate (0.43 6 g, 1.345 rnmol). The resulting wine colored mixture was heated at reflux under nitrogen for 20 hours. The reaction mixture was cooled to room temperature and concentrated. The crude mixture was purified by flash chromatography on silica gel using a gradient of 100:0 to 95:5 methylene chloride: methanol to afford the desired product as a WO 02/055014 PCT/SE02/00070 -130yellow solid (96.9 mng, 1 H NMR (300 MHz, DMSO, d 6 5 10.06 1 H, C(O)INH), 7.69 2H, J=9.0 Hz, ArIH'& H 6 7.58 (s,l1H, ArI-), 7.58 2H, J=9.O Hz, Hiy 6.95 1 H, Jm' 2.7 Hz, ArIL), 6.76 1 H, 2.7 Hz, -ArH 7 3.90 3 H, 0C11 3 3.75 (t, 4H, J= 4.8 Hz, OCH2CH 2 3.37 (bs, 4 H, ArNCjH 2 N,31 t 4.8 Hz,
OCH
2
CH
2 3.01 6 H, N(CH 3 2.71 (bs, 4 H, ArNCH 2 CH9N), 2.35 3 H, R 2 NCHj 3 Mass Spec.: cale. for [C 2 sH 36
N
6
O
3 Theor. mn/z =505; Obs. 505.5.
Example 99 H
N
H
N)
NN
6-Methoxy-4-methylamino-8-(4-methyl-piperazin-1I-yl)-quinoline-2-carboxylic acid (4morpholin-4-yl-phenyl)-amide.
The title compound was prepared from 8-bfbmo-6-methoxy-4-oxo-1,4-dihydroquinoline-2-carboxylic acid (Reference Example 27b) according to the procedure described for Example 98 using N-methyl amine to prepare 8-bromo-4-methylamino-6-methoxyquinoline-2-carboxylic acid (4-morpholini-4-yl-phenyl)-amide. A glassy orange solid was obtained. Mass Spec.: caic. for [C 27
H
34
N
6
O
3 Theor. m/z 491; Obs. 491.5.
Example 100 0~ F 1 1-: N N
N.
N)0N 0
NN
I0 6-Fluoro-4-miethoxy-8-(4-nieth-yl-piperazin- 1 -yl)-quinoline-2-carboxylic acid (4-morpholin-4yl-phenyl)-ainide.
Into a 250 mL round bottom flaskc equipped with a nitrogen inlet and magnetic stirrer is added 2.0 1 g (6.3 rnmol, 1.0 equiv.) of 6-Fltuoro-4-methoxy-8-(4-methyl-piperazin-1-yl)- WO 02/055014 PCT/SE02/00070 -131quinoline-2-carboxylic acid hydrochloride salt. This material is dissolved in 20 mL of DMF and then 1.35 g (7.56 mmol, 1.2 equiv.) of 4-morpholinoaniline is added. To the stirred solution is quickly added simultaneously added 4.05g (12.6 mmol, 2.0 equiv.) of TBTU (2- (1H-benzotriazole-1-yl)-l,1,3,3tetramethyluroniumtetrafluoroborate) and 1.7 g (12.6 mmol, 2.0 equiv.) of HOBT (1-hydroxybenzotriaole hydrate). At this point 3.25 g, 4.11 mL (25.2 mmol, 4.0 equiv.) is added via syringe over 5 minutes. The reaction is allowed to stir at room temperature for 18 hrs, then is concentrated on a rotary evaporator under high vacuum in.
order to remove the DMF. The residue is triturated with methanol and the crude solids are recovered by filtration. The material is then dissolved in methylene chloride and extracted with 10% sodium bicarbonate solution. The organic layer is dried and then concentrated.
These residues are then purified by flash chromatography using a gradient of 5-10% methanol in methylene chloride as eluent. The material which is obtained from chromatography, is then crystallized from methanol to give the pure product as 2.83g of a yellow solid.
Mass Spec.: calc. for [C 2 6
H
30 FNsO 3 +H] Theor. m/z 480; Obs. 480 Example 101 6-Fluoro-4-oxo-8-piperazin-1 -yl-4H-chromene-2-carboxylic acid (4-morpholin-4-yl-phenyl)amide: made according to the general method of Howarth et. al. Tetrahedron, 1998, 54, 10899-10914.
Dry 6-flouro-8-(4-methyl-piperazin-1-yl)-4-oxo-4H-chromene-2-carboxylic acid propionyl-piperazin-1-yl)-phenyl]-amide (Example 72)(1 g 1.9 mmol) was added to 100 mL of rigorously dried 1,2-dichloroethane in a flask under N 2 atmosphere and magnetic stirring.
The mixture was cooled to 0 6 C and freshly distilled 1-chloroethyl chloroformate (650 ul, 858 mg, 6 mmol, 3 eq) was added drop wise. The reaction was then heated under reflux for hours at which time LC/MS revealed complete consumption of starting material. Nal (Ig, leq) was added and heating continued for 2 days more. The reaction was then allowed to cool and filtered and evaporated to dryness under reduced pressure. MeOH (100 mL) was added and heated to reflux for 4h, filtered hot and evaporated to dryness. The product was isolated by chromatography using silica gel and CHC13/5% MeOH as an eluent. This gave 700 mg of the product HC1 salt as a yellow solid. LCMS m/z 508.
004592832 132 As used herein, the term "comprise" and variations of the term, such as C1 "comprising", "comprises" and "comprised", are not intended to exclude other additives, Ct components, integers or steps.
Reference to any prior art in the specification is not, and should not be taken as, an acknowledgement or any form of suggestion that this prior art forms part of the I'n common general knowledge in Australia or any other jurisdiction or that this prior art In could reasonably be expected to be ascertained, understood and regarded as relevant N by a person skilled in the art.
Claims (7)
133- THE CLAIMS DEFINING THE INVENTION ARE AS FOLLOWS: 1. A compound represented by the formula wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl; R 2 is represented by N, (CH 2 )n N R 3 is independently at each position represented by optionally substituted Cl_ 6 alkyl, optionally substituted C2-6alkenyl, optionally substituted C2- 6 alkynyl, optionally substituted C 3 _6cycloalkyl or AOH; nis2, 3 or4; 005005043
134- R6 R 6 is -H or methyl; Y is CH 2 NH-, c 2 -CH 2 -C(=O)-piperazine-, -CH 2 NA-, -NACH 2 or a 5-membered heterocycle; R7 t 5 R is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one c' or more substituents selected from R-R 9 and R 1 0 wherein R 7 is connected to Y either by a Cr single bond or by a ring fusion; O R 8 is -CH 2 -SO 2 -S02NH-, a single bond as tether from R 7 to R 9 5-membered heterocycle connected to R 7 by a ring fusion or a single bond as tether; R 9 is optionally substituted heterocycle, optionally substituted aryl, optionally substituted piperazinyl-R"', optionally substituted morpholinyl-R'", optionally substituted thiomorpholinyl, or R' 0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, C(=O)NHA, C(=O)NA 2 or OA; R" is alkyl, AOH, -SO 2 A, -SO 2 NH 2 -SO 2 NHA, -SO 2 NA 2 -SO 2 NHAR 9 -C(=O)R 9 -alkylR 9 C(=O)NH 2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA; or a pharmaceutically acceptable salt of said compound. 2. A compound according to claim 1, wherein R 2 is N-methylpiperazine-4-yl. 3. A method of treating migraine by administering a therapeutically effective amount of a compound according to claim 1 or claim 2, to a human or animal in need of such therapy. 005005043
135- 4. A pharmaceutical composition comprising a compound according to claim 1 or claim 2, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. A method of treatment of a human or animal suffering from migraine including administering to such human or animal an effective amount of a compound according to claim 1 or claim 2, or a pharmaceutically acceptable salt of said compound. 6. A compound of Formula (VIfl); HCI Vlfl wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkenyl; R 2 is represented by (CH 2 )n C N 005005043 -136- R 3 is independently at each position represented by optionally substituted Ci.salkyl, optionally substituted C2-6alkenyl, optionally substituted C2-6alkynyl, optionally substituted C 3 .6cycloalkyl or AOH; nis2, 3 or 4; 5 and X is represented by O, or a pharmaceutically acceptable salt thereof. 7. A compound according to claim 6, wherein R 2 is N-methylpiperazine-4-yl. 8. A process for preparing a compound of formula (VIfl) In In In HCI Vlfl according to claim 6, comprising heating a compound of Formula (VIe), wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 005005043 -137- O C -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or Saryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkenyl; n 5 R 2 is represented by N (n I (CH 2 )n S/ N (i) R 3 R 3 is independently at each position represented by optionally substituted C 1 6 alkyl, optionally substituted C2-6alkenyl, optionally substituted C2-6alkynyl, optionally substituted C 3 6 cycloalkyl or AOH; nis2, 3 or4; and R is CI-C 4 alkyl; in the presence of an acid and water to form a mixture wherein the mixture is hydrogenated using a catalyst. 9. A process according to claim 8, wherein the catalyst is palladium. 10. A compound of Formula (VIgl) 005005043
138- J R 1 L R 2 O HCI c VIgi wherein R 1 is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl; L represents a leaving group; R 2 is represented by Nr (CH 2 )n N (i) R 3 R 3 is independently at each position represented by optionally substituted Ci- 6 alkyl, optionally substituted C 2 6 alkenyl, optionally substituted C 2 .6alkynyl, optionally substituted C 3 6 cycloalkyl or AOH; n is 2, 3 or 4; and X is represented by O; or a pharmaceutically acceptable salt thereof. 005005043
139- 11. A compound according to claim 10, wherein R 2 is N-methylpiperazine-4-yl. 12. A process for preparing a compound of Formula (VIgl) HCI VIgl according to claim 10, comprising replacing the hydroxyl group of the carbpxylate moiety of Formula (VIfl)with a leaving group. 13. A compound of Formula (VIh XR1 R R 2 O VIMh wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl; 005005043
140- R 2 R 2 is represented by N (CH 2 )n SN (i) R 3 R 3 is independently at each position represented by optionally substituted Cl- 6 alkyl, optionally substituted C26alkenyl, optionally substituted C2-6alkynyl, optionally substituted C 3 -6cycloalkyl or AOH; nis2, 3 or 4; R 7 is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R 8 -R 9 and Ro 0 R 8 is -CH 2 -SO 2 -SO 2 NH-, a five membered heterocycle connected to R 7 by a ring fusion or single bond as tether; R 9 is morpholine optionally substituted with at least one substituent selected from A, thiomorpholino, piperazine-R", optionally substituted aryl, optionally substituted heterocyclyl, or -C(=O)CA; R 1 0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, -C(=O)NHA, -C(=O)NA 2 or OA; R" is alkyl, AOH, -SO 2 A, -S02NH 2 -SO 2 NHA, -S02NA 2 -S02NHAR 9 -C(=O)R 9 -alkylR 9 C(=O)NH 2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA; and X is represented by O; or a pharmaceutically acceptable salt of said compound. 14. A compound according to claim 13, wherein R 2 is N-methylpiperazine-4-yl. 005005043 141 A process for preparing a compound of Formula (Vlhl) R' R 2 O VIhI according to claim 13, comprising reacting a compound of(VIfl) Vlfl wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkenyl; R 2 is represented by 005005043 -142- NN (CH 2 )n e N (i) R3 t R 3 is independently at each position represented by optionally substituted Cil 6 alkyl, Soptionally substituted C 2 6 alkenyl, optionally substituted C 2 z 6 alkynyl, optionally substituted SC 3 6 cycloalkyl or AOH; nis2,30or4; and X is represented by O; with H 2 NR 7 wherein R 7 is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R 8 -R 9 and Ri 0 R 8 is -CH 2 -SO 2 -SO 2 NH-, a five membered heterocyclel connected to R 7 by a ring fusion or single bond as tether; R 9 is morpholine optionally substituted with at least one substituent selected from A, thiomorpholino, piperazine-R", optionally substituted aryl, optionally substituted heterocyclyl, or -C(=0)CA; R 1 0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, -C(=O)NH 2 methylthio, -NHA, -NA 2 -NHC(=O)A, -C(=O)NHA, -C(=O)NA 2 or OA; R" is alkyl, AOH, -SO 2 A, -SO 2 NH 2 -SO 2 NHA, -SO 2 NA 2 -SO 2 NHAR 9 -C(=O0)R 9 -alkylR 9 C(=O)NH 2 C(=O)NHA, C(=O)NA 2 or -C(=O)OA. 16. A process for preparing a compound of Formula (VIhl) 005005043 H .R >R7 VIhl according to claim 13, comprising reacting a compound of Formula (VIgl) R' ,L HCI VIgl wherein R' is, at each position, independently represented by hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, methoxy, thiomethoxy, -NHA, -NA 2 -NHC(=O)A, aminocarbonyl, -C(=O)NHA, -C(=O)NA 2 halogen, hydroxy, -OA, cyano or aryl; A is optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted alkenyl or optionally substituted alkynyl; L represents a leaving group; R 2 is represented by 005005043
144- N( SZ (CH 2 )n N (i) R 3 R 3 is independently at each position represented by optionally substituted C 1 i 6 alkyl, optionally substituted C2- 6 alkenyl, optionally substituted C2-6alkynyl, optionally substituted C 3 .6cycloalkyl or AOH; nis2, 3 or4; and X is represented by O; or a pharmaceutically acceptable salt thereof. with H 2 NR 7 wherein R 7 is a monocyclic or bicyclic aromatic ring or a heterocycle, optionally substituted by one or more substituents selected from R 8 -R 9 and R 8 is -CH 2 -SO 2 -SO 2 NH-, a five membered heterocycle connected to R 7 by a ring fusion or single bond as tether; R 9 is morpholine optionally substituted with at least one substituent selected from A, thiomorpholino, piperazine-R", optionally substituted aryl, optionally substituted heterocyclyl, or -C(=O)CA; R 1 0 is optionally substituted alkyl, optionally substituted cycloalkyl, hydroxy, aryl, cyano, halogen, methylthio, -NHA, -NA 2 -NHC(=O)A, -C(=0)NHA, -C(=0)NA 2 or OA; R" is alkyl, AOH, -SO 2 A, -SO 2 NH 2 -SO 2 NHA, -SO 2 NA 2 -SO 2 NHAR 9 -C(=0)R 9 -alkylR 9 C(=O)NH 2 C(=O)NHA, C(=O)NA 2 or -C(=0)OA. 17. A compound of the formula: 005102365 -145- or a pharmaceutically acceptable salt thereof, and/or a tautomer thereof, and/or a hydrate thereof, and/or a solvate thereof, and/or a steroisomer thereof. 18. A compound of the formula or a pharmaceutically acceptable salt thereof, and/or a tautomer thereof, and/or a hydrate thereof, and/or a solvate thereof, and/or a steroisomer thereof. 19. A pharmaceutical composition comprising a compound according to claim 18, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 20. A method of treatment of a human or animal suffering from migraine including administering to such human or animal an effective amount of a compound according to claim 18, or a pharmaceutically acceptable salt of said compound. 21. A compound according to any one of claims 1, 6, 10, or 13 substantially as hereinbefore described with reference to any one of the examples.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26210801P | 2001-01-16 | 2001-01-16 | |
| US60/262,108 | 2001-01-16 | ||
| SE0103646-6 | 2001-11-01 | ||
| SE0103646A SE0103646D0 (en) | 2001-11-01 | 2001-11-01 | Therapeutic chroman compounds |
| PCT/SE2002/000070 WO2002055014A2 (en) | 2001-01-16 | 2002-01-15 | Therapeutic chroman compounds |
Publications (3)
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| AU2002225551A1 AU2002225551A1 (en) | 2003-02-06 |
| AU2002225551B2 AU2002225551B2 (en) | 2008-04-03 |
| AU2002225551B8 true AU2002225551B8 (en) | 2008-05-29 |
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ID=26655581
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| Application Number | Title | Priority Date | Filing Date |
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| AU2002225551A Ceased AU2002225551B8 (en) | 2001-01-16 | 2002-01-15 | Therapeutic chroman compounds |
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| EP (1) | EP1353915A2 (en) |
| JP (1) | JP4280068B2 (en) |
| KR (1) | KR20030070917A (en) |
| CN (1) | CN100384833C (en) |
| AR (1) | AR036327A1 (en) |
| AU (1) | AU2002225551B8 (en) |
| BR (1) | BR0206514A (en) |
| CA (1) | CA2434015A1 (en) |
| IL (3) | IL156601A0 (en) |
| MX (1) | MXPA03006261A (en) |
| MY (1) | MY138263A (en) |
| NO (1) | NO20033205L (en) |
| NZ (1) | NZ526699A (en) |
| SA (1) | SA02220709B1 (en) |
| WO (1) | WO2002055014A2 (en) |
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| CA2668822C (en) | 1996-08-08 | 2011-03-15 | Hitachi Chemical Company, Ltd. | Graphite particles and lithium secondary cell using them as negative electrode |
| SE0103649D0 (en) * | 2001-11-01 | 2001-11-01 | Astrazeneca Ab | Therapeutic quinoline compounds |
| TWI349666B (en) | 2004-03-12 | 2011-10-01 | Lundbeck & Co As H | Substituted morpholine and thiomorpholine derivatives |
| EP2316458A1 (en) | 2004-09-20 | 2011-05-04 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
| AU2005286793A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-CoA desaturase enzymes |
| MX2007003325A (en) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors. |
| AU2005286648A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
| CN101084212A (en) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | Heterocyclic derivatives and their use as mediators of stearoyl-coa desaturase |
| CN101083993A (en) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | Heterocyclic derivatives and their use as therapeutic agents |
| US7777036B2 (en) | 2004-09-20 | 2010-08-17 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as therapeutic agents |
| BRPI0611187A2 (en) | 2005-06-03 | 2010-08-24 | Xenon Pharmaceuticals Inc | amino thiazide derivatives as inhibitors of human stearoyl coa desaturase |
| UY29892A1 (en) * | 2005-11-04 | 2007-06-29 | Astrazeneca Ab | NEW CHROMAN DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, PREPARATION PROCESSES AND APPLICATIONS |
| CA2632512A1 (en) | 2005-12-08 | 2007-06-14 | Millennium Pharmaceuticals, Inc. | Bicyclic compounds with kinase inhibitory activity |
| AR059356A1 (en) * | 2006-02-14 | 2008-03-26 | Astrazeneca Ab | NEW RADIOLIGANDS |
| WO2007097697A1 (en) * | 2006-02-23 | 2007-08-30 | Astrazeneca Ab | Therapeutic quinoline compounds that are 5ht1b modulators |
| US7812206B2 (en) | 2006-03-21 | 2010-10-12 | Bp Corporation North America Inc. | Apparatus and process for the separation of solids and liquids |
| US8530716B2 (en) | 2008-08-14 | 2013-09-10 | Bp Corporation North America Inc. | Melt-crystallization separation and purification process |
| HUP0900281A2 (en) * | 2009-05-05 | 2011-01-28 | Univ Szegedi | Kynurenc acid derivatives, process for their preparation, pharmaceutical compositions containing them and their use for the treatment of headache |
| US9630896B2 (en) | 2013-11-22 | 2017-04-25 | Tansna Therapeutics, Inc. | 2,5-dialkyl-4-H/halo/ether-phenol compounds |
| CN104262249A (en) * | 2014-10-20 | 2015-01-07 | 云南民族大学 | Environmental-friendly and efficient preparation method of quinolone compound |
| WO2017210545A1 (en) | 2016-06-02 | 2017-12-07 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| PT3571193T (en) | 2017-01-23 | 2022-03-25 | Cadent Therapeutics Inc | Potassium channel modulators |
| US11993586B2 (en) | 2018-10-22 | 2024-05-28 | Novartis Ag | Crystalline forms of potassium channel modulators |
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| GB8515389D0 (en) * | 1985-06-18 | 1985-07-17 | Ici Plc | Heterocyclic compounds |
| US5112856A (en) * | 1986-08-15 | 1992-05-12 | Hoffmann-La Roche Inc. | Therapeutic treatment of intestinal inflammation by administration of 3,4-dihydro-2H-1-benzopyran derivatives |
| SE8904361D0 (en) * | 1989-12-22 | 1989-12-22 | Astra Ab | NEW CHROMAN AND THIOCHROMAN DERIVATIVES |
| DE4140542A1 (en) * | 1991-12-09 | 1993-06-17 | Bayer Ag | PIPERDYLMETHYL SUBSTITUTED CHORMANDERIVATE |
| FR2761358B1 (en) * | 1997-03-27 | 1999-05-07 | Adir | NOVEL N-ARYL PIPERIDINE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| SE9703378D0 (en) * | 1997-09-18 | 1997-09-18 | Astra Ab | New compounds |
| FR2782515B1 (en) * | 1998-08-21 | 2000-09-22 | Adir | NEW INDANE-1-Ol DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
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- 2002-01-15 CA CA002434015A patent/CA2434015A1/en not_active Abandoned
- 2002-01-15 EP EP02715919A patent/EP1353915A2/en not_active Withdrawn
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Also Published As
| Publication number | Publication date |
|---|---|
| AU2002225551B2 (en) | 2008-04-03 |
| WO2002055014A3 (en) | 2002-11-14 |
| NO20033205L (en) | 2003-09-02 |
| JP2004517130A (en) | 2004-06-10 |
| CN1524077A (en) | 2004-08-25 |
| IL156601A (en) | 2009-06-15 |
| EP1353915A2 (en) | 2003-10-22 |
| CA2434015A1 (en) | 2002-07-18 |
| SA02220709B1 (en) | 2007-01-23 |
| IL183183A0 (en) | 2007-08-19 |
| MY138263A (en) | 2009-05-29 |
| JP4280068B2 (en) | 2009-06-17 |
| NZ526699A (en) | 2005-03-24 |
| WO2002055014A2 (en) | 2002-07-18 |
| AR036327A1 (en) | 2004-09-01 |
| CN100384833C (en) | 2008-04-30 |
| KR20030070917A (en) | 2003-09-02 |
| MXPA03006261A (en) | 2003-09-22 |
| BR0206514A (en) | 2004-01-06 |
| IL156601A0 (en) | 2004-01-04 |
| NO20033205D0 (en) | 2003-07-15 |
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