Amide derivatives as TTX-S blockers

Abstract

The present invention relates to amide derivatives which have blocking activities of voltage gated sodium channels as the TTX-S channels, and which are useful in the treatment or prevention of disorders and diseases in which voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which voltage gated sodium channels are involved. ##STR00001##

Claims

1. A compound of the following formula (I): ##STR01067## wherein: A is an aryl selected from the group consisting of phenyl, benzoimidazolyl, dihydroisoquinolyl, indolyl, indazolyl, pyrazolyl, pyrazinyl, pyridazinyl, pyridyl, quinolyl, isoquinolyl and thiazolyl; B is selected from the group consisting of a chemical bond, C.sub.1-6 alkylene-, OC.sub.1-6 alkylene-, and NR.sup.7; W is hydrogen, or C.sub.1-6 alkyl; Z is nitrogen atom or CH; R.sup.1 is fluorinated substituent independently selected from the group consisting of CF.sub.3, CHF.sub.2, OCF.sub.3, OCHF.sub.2, OCH.sub.2CHF.sub.2, OCH.sub.2CF.sub.3, OCF.sub.2CHF.sub.2, OCF.sub.2CF.sub.3, OCH.sub.2CH.sub.2CF.sub.3, OCH(CH.sub.3)CF.sub.3, OCH.sub.2C(CH.sub.3)F.sub.2, OCH.sub.2CF.sub.2CHF.sub.2, OCH.sub.2CF.sub.2CF.sub.3, OCH.sub.2CH.sub.2OCH.sub.2CF.sub.3, NHCH.sub.2CF.sub.3, SCF.sub.3, SCH.sub.2CF.sub.3, CH.sub.2CF.sub.3, C(CH.sub.3).sub.2CF.sub.3, CH.sub.2CH.sub.2CF.sub.3, CH.sub.2OCH.sub.2CF.sub.3, OCH.sub.2CH.sub.2OCF.sub.3, 4,4-difluoropiperidino, and (4-fluorobenzyl)oxy; R.sup.2 is independently selected from the group consisting of: (1) hydrogen, (2) halogen, (3) hydroxyl, (4) O.sub.nC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (5) O.sub.nC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (6) O.sub.nC.sub.2-4 alkenyl, where the alkenyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (7) O.sub.n-phenyl or O.sub.n naphthyl, where the phenyl or naphthyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (8) O.sub.n-heterocyclic group, where the heterocyclic group is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (9) (CO)NR.sup.8R.sup.9, (10) NR.sup.8R.sup.9, (11) S(O).sub.2NR.sup.8R.sup.9, (12) NR.sup.8S(O).sub.2R.sup.9, (13) S(O).sub.tR.sup.9, where t is 0, 1 or 2, (14) NR.sup.8(CO)R.sup.9, (15) CN, and (16) NO.sub.2; wherein n is 0 or 1; when n is 0, a chemical bond is present in the place of O.sub.n; p is 1, 2, 3, or 4; when p is two or more than two, R.sup.2 may be the same or different; R.sup.3 and R.sup.4 are independently hydrogen or C.sub.1-6 alkyl; R.sup.5 is independently selected from the group consisting of: (1) hydrogen, (2) halogen, (3) O.sub.nC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (4) O.sub.nC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, and (5) O.sub.nC.sub.2-4 alkenyl, where the alkenyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7; wherein n is 0 or 1; when n is 0, a chemical bond is present in the place of O.sub.n; q is 1, 2 or 3; when q is two or more than two, R.sup.5 may be the same or different; R.sup.6 is independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-7 cycloalkyl, or aryl, which is unsubstituted or substituted with one or more substituents independently selected from the group consisting of halogen, hydroxyl, C.sub.1-6 alkyl, OC.sub.1-6 alkyl, C.sub.3-7 cycloalkyl, and OC.sub.3-7 cycloalkyl; R.sup.7 in the definition of B and R.sup.2 is selected from the group consisting of: (1) hydrogen, (2) halogen, (3) hydroxyl, (4) (CO).sub.mO.sub.lC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (5) O.sub.l(C.sub.1-3)perfluoroalkyl, (6) (CO).sub.mO.sub.lC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (9) (CO).sub.mO.sub.l-heterocyclic group, where the heterocyclic group is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, and (11) NR.sup.8R.sup.9; wherein l is 0 or 1 and m is 0 or 1; when l is 0 or m is 0, a chemical bond is present in the place of O.sub.l or (CO).sub.m, and when l is 0 and m is 0, a chemical bond is present in the place of (CO).sub.mO.sub.l; R.sup.7 in the definition of R.sup.5 is selected from the group consisting of: (1) hydrogen, (2-1) chloro, (2-2) bromo, (2-3) iodo, (3) hydroxyl, (4) (CO).sub.mO.sub.lC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, and (6) (CO).sub.mO.sub.lC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10; wherein l is 0 or 1 and m is 0 or 1; when l is 0 or m is 0, a chemical bond is present in the place of O.sub.l or (CO).sub.m, and when l is 0 and m is 0, a chemical bond is present in the place of (CO).sub.mO.sub.l; R.sup.8 and R.sup.9 are independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-7 cycloalkyl, or aryl, which is unsubstituted or substituted with one or more substituents independently selected from the group consisting of halogen, hydroxyl, C.sub.1-6 alkyl, OC.sub.1-6 alkyl, C.sub.3-7 cycloalkyl, and OC.sub.3-7 cycloalkyl, wherein the aryl is a mono- or bi-carbocyclic or mono- or bi-heterocyclic ring which optionally contains 0 to 4 heteroatoms selected from the group consisting of O, N and S; or R.sup.8 forms a 4 to 7 membered ring with R.sup.9 which optionally contains a nitrogen atom, an oxygen atom, a sulfur atom or a double bond, wherein the 4 to 7 membered ring is optionally substituted with 1 to 6 substituents independently selected from the group consisting of: (1) hydrogen, (2) hydroxyl, (3) halogen, (4) C.sub.1-6 alkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (5) C.sub.3-6 cycloalkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (6) OC.sub.1-6 alkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, and (7) OC.sub.3-6 cycloalkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10; R.sup.10 is independently selected from the group consisting of: (1) hydrogen, (2) hydroxyl, (3) halogen, (4) C.sub.1-6 alkyl, (5) C.sub.3-6 cycloalkyl, (6) OC.sub.1-6 alkyl, (7) O(CO)C.sub.1-6 alkyl, (8) NHC.sub.1-6 alkyl, (9) phenyl, (10) heterocyclic group, and (11) CN, wherein the heterocyclic group is an unsaturated or saturated mono- or bi-heterocyclic ring which optionally contains 1 to 4 heteroatoms selected from the group consisting of O, N, and S, and wherein the cycloalkyl is a mono- or bicyclic ring selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and norboranyl; or a pharmaceutically acceptable salt thereof.

2. The compound according to claim 1, wherein B is a chemical bond; or a pharmaceutically acceptable salt thereof.

3. A compound of the following formula (II) ##STR01068## wherein: X is nitrogen atom, or CH; Y is nitrogen atom, or CH; Z is nitrogen atom, or CH; W is hydrogen, or C.sub.1-6 alkyl; R.sup.1 is a fluorinated substituent independently selected from the group consisting of CF.sub.3, CHF.sub.2, OCF.sub.3, OCHF.sub.2, OCH.sub.2CHF.sub.2, OCH.sub.2CF.sub.3, OCF.sub.2CHF.sub.2, OCF.sub.2CF.sub.3, OCH.sub.2CH.sub.2CF.sub.3, OCH(CH.sub.3)CF.sub.3, OCH.sub.2C(CH.sub.3)F.sub.2, OCH.sub.2CF.sub.2CHF.sub.2, OCH.sub.2CF.sub.2CF.sub.3, OCH.sub.2CH.sub.2OCH.sub.2CF.sub.3, NHCH.sub.2CF.sub.3, SCF.sub.3, SCH.sub.2CF.sub.3, CH.sub.2CF.sub.3, C(CH.sub.3).sub.2CF.sub.3, CH.sub.2CH.sub.2CF.sub.3, CH.sub.2OCH.sub.2CF.sub.3, OCH.sub.2CH.sub.2OCF.sub.3, 4,4-difluoropiperidino, and (4-fluorobenzyl)oxy; R.sup.2 is independently selected from the group consisting of: (1) hydrogen, (2) halogen, (3) hydroxyl, (4) O.sub.nC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (5) O.sub.nC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (6) O.sub.nC.sub.2-4 alkenyl, where the alkenyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (7) O.sub.n-phenyl or O.sub.n naphthyl, where the phenyl or naphthyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (8) O.sub.n-heterocyclic group, where the heterocyclic group is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (9) (CO)NR.sup.8R.sup.9, (10) NR.sup.8R.sup.9, (11) S(O).sub.2NR.sup.8R.sup.9, (12) NR.sup.8S(O).sub.2R.sup.9, (13) S(O).sub.tR.sup.9, where t is 0, 1 or 2, (14) NR.sup.8(CO)R.sup.9, (15) CN, and (16) NO.sub.2; wherein n is 0 or 1; when n is 0, a chemical bond is present in the place of O.sub.n; p is 1, 2, 3, or 4; when p is two or more than two, R.sup.2 may be the same or different; R.sup.3 and R.sup.4 are independently hydrogen or C.sub.1-6 alkyl; R.sup.5 is independently selected from the group consisting of: (1) hydrogen, (2) halogen, (3) O.sub.nC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, (4) O.sub.nC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7, and (5) O.sub.nC.sub.2-4 alkenyl, where the alkenyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.7; wherein n is 0 or 1; when n is 0, a chemical bond is present in the place of O.sub.n; q is 1, 2 or 3; when q is two or more than two, R.sup.5 may be the same or different; R.sup.6 is independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-7 cycloalkyl, or aryl, which is unsubstituted or substituted with one or more substituents independently selected from the group consisting of halogen, hydroxyl, C.sub.1-6 alkyl, OC.sub.1-6 alkyl, C.sub.3-7 cycloalkyl, and OC.sub.3-7 cycloalkyl; R.sup.7 in the definition of R.sup.2 is selected from the group consisting of: (1) hydrogen, (2) halogen, (3) hydroxyl, (4) (CO).sub.mO.sub.lC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (5) O.sub.l(C.sub.1-3)perfluoroalkyl, (6) (CO).sub.mO.sub.lC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (9) (CO).sub.mO.sub.l-heterocyclic group, where the heterocyclic group is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, and (11) NR.sup.8R.sup.9; wherein l is 0 or 1 and m is 0 or 1; when l is 0 or m is 0, a chemical bond is present in the place of O.sub.l or (CO).sub.m, and when l is 0 and m is 0, a chemical bond is present in the place of (CO).sub.mO.sub.l; R.sup.7 in the definition of R.sup.5 is selected from the group consisting of: (1) hydrogen, (2-1) chloro, (2-2) bromo, (2-3) iodo, (3) hydroxyl, (4) (CO).sub.mO.sub.lC.sub.1-6 alkyl, where the alkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, and (6) (CO).sub.mO.sub.lC.sub.3-6 cycloalkyl, where the cycloalkyl is unsubstituted or substituted with one or more substituents independently selected from R.sup.10; wherein l is 0 or 1 and m is 0 or 1; when l is 0 or m is 0, a chemical bond is present in the place of O.sub.l or (CO).sub.m, and when l is 0 and m is 0, a chemical bond is present in the place of (CO).sub.mO.sub.l; R.sup.8 and R.sup.9 are independently hydrogen, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.3-7 cycloalkyl, or aryl, which is unsubstituted or substituted with one or more substituents independently selected from the group consisting of halogen, hydroxyl, C.sub.1-6 alkyl, OC.sub.1-6 alkyl, C.sub.3-7 cycloalkyl, and OC.sub.3-7 cycloalkyl, wherein the aryl is a mono- or bi-carbocyclic or mono- or bi-heterocyclic ring which optionally contains 0 to 4 heteroatoms selected from the group consisting of O, N and S; or R.sup.8 forms a 4 to 7 membered ring with R.sup.9 which optionally contains a nitrogen atom, an oxygen atom, a sulfur atom or a double bond, wherein the 4 to 7 membered ring is optionally substituted with 1 to 6 substituents independently selected from the group consisting of: (1) hydrogen, (2) hydroxyl, (3) halogen, (4) C.sub.1-6 alkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (5) C.sub.3-6 cycloalkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, (6) OC.sub.1-6 alkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10, and (7) OC.sub.3-6 cycloalkyl, which is unsubstituted or substituted with one or more substituents independently selected from R.sup.10; R.sup.10 is independently selected from the group consisting of: (1) hydrogen, (2) hydroxyl, (3) halogen, (4) C.sub.1-6 alkyl, (5) C.sub.3-6 cycloalkyl, (6) OC.sub.1-6 alkyl, (7) O(CO)C.sub.1-6 alkyl, (8) NHC.sub.1-6 alkyl, (9) phenyl, (10) heterocyclic group, and (11) CN, wherein the heterocyclic group is an unsaturated or saturated mono- or bi-heterocyclic ring which optionally contains 1 to 4 heteroatoms selected from the group consisting of O, N, and S, and wherein the cycloalkyl is a mono- or bicyclic ring selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and norboranyl; or a pharmaceutically acceptable salt thereof.

4. The compound according to claim 3, wherein Z is CH; or a pharmaceutically acceptable salt thereof.

5. The compound according to claim 4, wherein: R.sup.1 is selected from the group consisting of CF.sub.3, OCF.sub.3, OCH.sub.2CHF.sub.2, OCH.sub.2C(CH.sub.3)F.sub.2, CH.sub.2CH.sub.2CF.sub.3, OCF.sub.2CHF.sub.2, OCF.sub.2CF.sub.3, OCH.sub.2CF.sub.2CF.sub.3, OCH.sub.2CF.sub.2CHF.sub.2 and OCH.sub.2CF.sub.3; R.sup.2 is independently selected from the group consisting of: (1) hydrogen, (2) halogen, (3) methyl, and (4) methoxy; p is 1; R.sup.3 is hydrogen; R.sup.4 is hydrogen or methyl; W is hydrogen; R.sup.6 is selected from the group consisting of methyl, ethyl, isopropyl, and cyclopropyl; or a pharmaceutically acceptable salt thereof.

6. The compound according to claim 1, which is selected from the group consisting of: N-((2-acetamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-(cyclopropanecarboxamido)pyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-benzamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-methyl-N-((2-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-chloro-N-((2-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-propionamidopyridin-4-yl)methyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-((2-isobutyramidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-(cyclobutanecarboxamido)pyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-propionamidopyridin-4-yl)methyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; 2-methoxy-N-((2-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-methyl-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-chloro-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-fluoro-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-(cyclopropanecarboxamido)pyridin-4-yl)methyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; 4-methyl-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-methoxy-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-((2-propionamidopyridin-4-yl)methyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-methyl-6-propionamidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyrimidin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyrimidin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyrimidin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(6-methyl-2-propionamidopyrimidin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)-6-methylpyrimidin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyrimidin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)-6-methylpyrimidin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-methyl-N-(1-(6-methyl-2-propionamidopyrimidin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-methyl-6-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropyl)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-chloro-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-chloro-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(2,2-difluoroethoxy)-3-methylbenzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2-difluoroethoxy)-5-methylnicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; 6-(2,2-difluoroethoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methylnicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropyl)nicotinamide; N-(4-(1-(2-(4-(trifluoromethyl)phenyl)acetamido)ethyl)pyridin-2-yl)isobutyramide; N-(4-(1-(2-(4-(trifluoromethoxy)phenyl)acetamido)ethyl)pyridin-2-yl)isobutyramide; N-(4-(1-(2-(4-(trifluoromethyl)phenoxy)acetamido)ethyl)pyridin-2-yl)isobutyramide; N-(4-(1-(2-(2-(trifluoromethyl)phenoxy)acetamido)ethyl)pyridin-2-yl)isobutyramide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(perfluoroethoxy)benzamide; N-(4-(1-(3-(4-(trifluoromethoxy)phenyl)ureido)ethyl)pyridin-2-yl)isobutyramide; 5-chloro-N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-fluoro-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropyl)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-3-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; N-(4-(1-(2-(4-(trifluoromethyl)phenyl)acetamido)ethyl)pyridin-2-yl)cyclopropanecarboxamide; N-(4-(1-(2-(4-(trifluoromethyl)phenoxy)acetamido)ethyl)pyridin-2-yl)cyclopropanecarboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-2-(1,1,1-trifluoro-2-methylpropan-2-yl)quinoline-6-carboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-(trifluoromethoxy)-1H-indole-2-carboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(trifluoromethoxy)-1H-indazole-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2, 3,3,3-pentafluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(perfluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(4-(trifluoromethyl)phenoxy)acetamide; N-(1-(6-methyl-2-propionamidopyrimidin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyrimidin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; 5-chloro-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 5-fluoro-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 6-(2,2-difluoroethoxy)-5-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)nicotinamide; 2-methoxy-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropyl)nicotinamide; 4-(perfluoroethoxy)-N-(1-(2-propionamidopyridin-4-yl)ethyl)benzamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-3-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-4-(1,1,2,2-tetrafluoroethoxy)benzamide; 5-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2, 3,3-tetrafluoropropoxy)nicotinamide; 6-(2,2,3,3,3-pentafluoropropoxy)-N-(1-(2-propionamidopyridin-4-yl)ethyl)nicotinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; 4-(2,2-difluoroethoxy)-3-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)benzamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-methyl-2-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-4-((2,2,2-trifluoroethoxy)methyl)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-((2,2,2-trifluoroethoxy)methyl)benzamide; N-(1-(2-(3-methylbutanamido)pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-fluoro-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyrimidin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-methoxy-N-(1-(6-methyl-2-propionamidopyrimidin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)-6-methylpyrimidin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyrimidin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(3,3,3-trifluoropropoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(4-(trifluoromethyl)phenoxy)propanamide; 6-(2,2,3,3,3-pentafluoropropoxy)-N-(1-(2-propionamidopyridin-4-yl)ethyl)pyridazine-3-carboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyrimidin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclobutanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acrylamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(3,3,3-trifluoropropoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methyl-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(3,3,3-trifluoropropoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-(3,3,3-trifluoropropoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-methyl-6-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-(cyclopropanecarboxamido)-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-3-methyl-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-methyl-4-(2,2,2-trifluoroethoxy)benzamide; 5-(2,2,3,3,3-pentafluoropropoxy)-N-(1-(2-propionamidopyridin-4-yl)ethyl)picolinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-(cyclobutanecarboxamido)pyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acrylamidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-(cyclohexanecarboxamido)pyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-pivalamidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-butyramidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(4-(1-(3-(3-(trifluoromethyl)phenyl)ureido)ethyl)pyridin-2-yl)isobutyramide; N-(4-(1-(3-(4-(trifluoromethyl)phenyl)ureido)ethyl)pyridin-2-yl)isobutyramide; N-(6-methyl-4-(1-(3-(4-(trifluoromethoxy)phenyl)ureido)ethyl)pyridin-2-yl)acetamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(cyclobutanecarboxamido)pyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2-difluoropropoxy)nicotinamide; 6-(2,2-difluoropropoxy)-N-(1-(2-propionamidopyridin-4-yl)ethyl)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2-difluoropropoxy)nicotinamide; 6-(2,2-difluoropropoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)nicotinamide; 2-hydroxy-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(trifluoromethyl)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-methoxy-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-2-methoxy-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-methoxy-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2-difluoroethoxy)-2-methoxynicotinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-(2,2-difluoroethoxy)-2-methoxynicotinamide; 6-(2,2-difluoroethoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-methoxynicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(trifluoromethyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-1-methyl-5-(2,2,2-trifluoroethoxy)-1H-pyrazole-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropyl)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; 6-(2,2-difluoroethoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-methoxynicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-methoxy-6-(3,3,3-trifluoropropoxy)nicotinamide; 6-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; 2-fluoro-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-3-methyl-4-(2,2,2-trifluoroethoxy)benzamide; 3-chloro-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; 4-(2,2-difluoroethoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-3-methylbenzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(3,3,3-trifluoropropoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(perfluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(piperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(piperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-morpholino-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-morpholino-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-morpholino-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(4-methoxypiperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(4-methoxypiperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-(4-methoxypiperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-((2-methoxyethyl)(methyl)amino)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-((2-methoxyethyl)(methyl)amino)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2,6-bis(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2,6-bis(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2,6-bis(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(2-methoxyethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(2-methoxyethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-(2-methoxyethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(2,2-difluoroethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(2,2-difluoroethoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(2,2-difluoroethoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-methoxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-3-methoxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-3-methoxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-hydroxy-4-(trifluoromethyl)benzamide; 2-hydroxy-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(trifluoromethyl)benzamide; 2-hydroxy-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; 2-hydroxy-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(4-fluorophenoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(4-fluorophenoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(4-fluorophenoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-methoxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-methoxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-methoxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-(cyclopropanecarboxamido)-6-methoxypyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methoxypyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-((2,2,2-trifluoroethoxy)methyl)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-((2,2,2-trifluoroethoxy)methyl)benzamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-2-(piperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-2-morpholino-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(4-fluorophenoxy)-N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methyl pyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-2-(2-methoxyethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-2, 6-bis(2,2,2-trifluoroethoxy)nicotinamide; 2-(2,2-difluoroethoxy)-N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-2-(4-(trifluoromethyl)phenyl)thiazole-4-carboxamide; 3-chloro-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; 3-chloro-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-chloro-4-(trifluoromethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-hydroxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(4-methylpiperazin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(4-hydroxypiperidin-1-yl)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(4-hydroxypiperidin-1-yl)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-(4-fluorophenyl)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(4-fluorophenyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(3-methoxypropoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-(3-methoxypropoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(3-methoxypropoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-hydroxy-N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(2-(2-oxopyrrolidin-1-yl)ethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-(2-(2-oxopyrrolidin-1-yl)ethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-1-methyl-5-(2,2,3,3,3-pentafluoropropoxy)-1H-pyrazole-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-1-methyl-5-(2,2,3,3,3-pentafluoropropoxy)-1H-pyrazole-3-carboxamide; 1-methyl-5-(2,2,3,3,3-pentafluoropropoxy)-N-(1-(2-propionamidopyridin-4-yl)ethyl)-1H-pyrazole-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-methoxy-4-(trifluoromethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-methoxy-4-(trifluoromethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-methoxy-4-(trifluoromethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-hydroxy-4-(trifluoromethoxy)benzamide; 2-hydroxy-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; 2-hydroxy-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(trifluoromethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-(2-morpholinoethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-2-(2-morpholinoethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-(2-morpholinoethoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-fluoro-4-(trifluoromethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-(cyclopropanecarboxamido)pyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; 4-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; 5-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)pyrazine-2-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)pyrazine-2-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-((2,2,2-trifluoroethyl)amino)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2-(2,2,2-trifluoroethoxy)ethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2-(2,2,2-trifluoroethoxy)ethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2-difluoropropoxy)-5-methylnicotinamide; 6-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methylnicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-(2,2-difluoroethoxy)-4-methylpicolinamide; 5-(2,2-difluoroethoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-methylpicolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-methyl-5-(3,3,3-trifluoropropoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-methyl-5-(3,3,3-trifluoropropoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-3-methyl-4-(trifluoromethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-3-methyl-4-(trifluoromethoxy)benzamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-1-(2,2,2-trifluoroethoxy)isoquinoline-4-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-((2,2,2-trifluoroethoxy)methyl)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(3,3,3-trifluoropropyl)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(3,3,3-trifluoropropyl)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-chloro-6-(3,3,3-trifluoropropoxy)nicotinamide; 5-chloro-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-chloro-6-(2,2-difluoropropoxy)nicotinamide; 5-chloro-6-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-((4-fluorobenzyl)oxy)-5-methylnicotinamide; 6-((4-fluorobenzyl)oxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methylnicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(4,4-difluoropiperidin-1-yl)-5-methylnicotinamide; 6-(4,4-difluoropiperidin-1-yl)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methylnicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)pyrazine-2-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-(2,2-difluoropropoxy)-5-methylnicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-chloro-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-(trifluoromethyl)-1H-benzo[d]imidazole-2-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-((4-fluorobenzyl)oxy)-5-methylnicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-methyl-5-(2,2,2-trifluoroethoxy)pyrazine-2-carboxamide; 6-(2,2-difluoropropoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methylnicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(trifluoromethyl)-1H-benzo[d]imidazole-2-carboxamide; 6-((4-fluorobenzyl)oxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methylnicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-(2,2-difluoroethoxy)-4-methylpicolinamide; 5-(2,2-difluoroethoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methylpicolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(3,3,3-trifluoropropoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methyl-5-(3,3,3-trifluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-2-(4-fluorophenoxy)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-((4-fluorobenzyl)oxy)-4-methylpicolinamide; 5-((4-fluorobenzyl)oxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methylpicolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-(2,2-difluoropropoxy)-4-methylpicolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-(2,2-difluoropropoxy)-4-methylpicolinamide; 5-(2,2-difluoropropoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methylpicolinamide; 5-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-methylpicolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2-(trifluoromethoxy)ethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-methyl-6-(2-(trifluoromethoxy)ethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2-(trifluoromethoxy)ethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(trifluoromethyl)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-(2,2-difluoropropoxy)-3-methylbenzamide; 4-(2,2-difluoropropoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-3-methylbenzamide; 4-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-3-methylbenzamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-3-chloro-4-(2,2-difluoropropoxy)benzamide; 3-chloro-4-(2,2-difluoropropoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)benzamide; and 3-chloro-4-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)benzamide; or a pharmaceutically acceptable salt thereof.

7. The compound according to claim 1, which is selected from the group consisting of: 5-methyl-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; 2-methoxy-N-((2-methyl-6-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)nicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(3,3,3-trifluoropropyl)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-4-(perfluoroethoxy)benzamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,3,3,3-pentafluoropropoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-4-(perfluoroethoxy)benzamide; 2-hydroxy-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-(2,2,2-trifluoroethoxy)benzamide; 2-(2,2-difluoroethoxy)-N-(1-(2-(2-hydroxy-2-methylpropanamido)-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-2-hydroxy-4-(2,2,2-trifluoroethoxy)benzamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; 5-methyl-N-(1-(2-propionamidopyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2-difluoropropoxy)-5-methylnicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-chloro-6-(3,3,3-trifluoropropoxy)nicotinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-chloro-6-(2,2-difluoropropoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-(trifluoromethyl)-1H-benzo[d]imidazole-2-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-6-((4-fluorobenzyl)oxy)-5-methylnicotinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(trifluoromethyl)-1H-benzo[d]imidazole-2-carboxamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(3,3,3-trifluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-(2,2-difluoropropoxy)-4-methylpicolinamide; 5-(2,2-difluoropropoxy)-N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-4-methylpicolinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2-(trifluoromethoxy)ethoxy)nicotinamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-(2,2-difluoropropoxy)-3-methylbenzamide; and 4-(2,2-difluoropropoxy)-N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-3-methylbenzamide; or a pharmaceutically acceptable salt thereof.

8. A pharmaceutical composition comprising a compound or a pharmaceutically acceptable salt thereof, according to claim 1, and a pharmaceutically acceptable carrier.

9. The pharmaceutical composition according to claim 8, further comprising another pharmacologically active agent.

10. The compound according to claim 4, wherein either X or Y is nitrogen atom, and the other is CH or nitrogen atom, or a pharmaceutically acceptable salt thereof.

11. The compound according to claim 4, wherein either X or Y is nitrogen atom, and the other is CH, or a pharmaceutically acceptable salt thereof.

12. The compound according to claim 7, which is selected from the group consisting of: N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-5-(2,2,2-trifluoroethoxy)picolinamide; N-(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinamide; N-(1-(2-isobutyramido-6-methylpyridin-4-yl)ethyl)-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxamide; N-(1-(2-acetamidopyridin-4-yl)ethyl)-4-methyl-5-(2,2,2-trifluoroethoxy)picolinamide; and N-(1-(2-acetamidopyridin-4-yl)ethyl)-5-methyl-6-(2,2,2-trifluoroethoxy)pyridazine-3-carboxamide, or a pharmaceutically acceptable salt thereof.

Description

DESCRIPTION OF EMBODIMENTS

(1) Examples of conditions or disorders mediated by TTX-S channels include, but are not limited to, TTX-S channels related diseases. The compounds of the present invention show the TTX-S channels blocking activity. The compounds of the present invention can show less toxicity, good absorption and distribution, good solubility, less protein binding affinity other than TTX-S channels, less drug-drug interaction, good metabolic stability, reduced inhibitory activity at HERG channel, and/or reduced QT prolongation.

(2) As appreciated by those of skill in the art, halogen or halo as used herein is intended to include fluoro, chloro, bromo and iodo. Similarly, 1-6, as in C.sub.1-6 is defined to identify the number as having 1, 2, 3, 4, 5 or 6. According to the definition, for example, C.sub.1-6, as in C.sub.1-6 alkyl is defined to identify the alkyl group as having 1, 2, 3, 4, 5 or 6 carbons. Similarly, C.sub.2-6 alkenyl is defined to identify the alkenyl group as having 2, 3, 4, 5 or 6 carbons.

(3) A group which is designated as being independently substituted with substituents may be independently substituted with multiple numbers of such substituents.

(4) The term fluorinated substituent, as used herein, means a fluorinated alkyl, fluorinated alkoxy, fluorinated alkylthio, fluorinated alkoxyalkyl, fluorinated alkoxyalkoxy, fluorinated alkylamino, fluorinated arylalkoxy, but not limited to, CF.sub.3, CHF.sub.2, OCF.sub.3, OCHF.sub.2, OCH.sub.2CHF.sub.2, OCH.sub.2CF.sub.3, OCF.sub.2CHF.sub.2, OCF.sub.2CF.sub.3, OCH.sub.2CH.sub.2CF.sub.3, OCH(CH.sub.3)CF.sub.3, OCH.sub.2C(CH.sub.3)F.sub.2, OCH.sub.2CF.sub.2CHF.sub.2, OCH.sub.2CF.sub.2CF.sub.3, OCH.sub.2CH.sub.2OCH.sub.2CF.sub.3, NHCH.sub.2CF.sub.3, SCF.sub.3, SCH.sub.2CF.sub.3, CH.sub.2CF.sub.3, C(CH.sub.3).sub.2CF.sub.3, CH.sub.2CH.sub.2CF.sub.3, CH.sub.2OCH.sub.2CF.sub.3, OCH.sub.2CH.sub.2OCF.sub.3, 4,4-difluoropiperidino, (4-fluorobenzyl)oxy, and the like.

(5) The term alkyl, as used herein, means a linear saturated monovalent hydrocarbon radical of one to six carbon atoms or a branched saturated monovalent hydrocarbon radical of three to six carbon atoms, e.g., methyl, ethyl, propyl, 2-propyl, butyl (including all isomeric forms), pentyl (including all isomeric forms), and the like.

(6) The term alkoxy, as used herein, means an O-alkyl, but not limited to, methoxy, ethoxy, propoxy, or 2-propoxy, butoxy (including all isomeric forms), and the like.

(7) The term alkylthio, as used herein, means a S-alkyl, but not limited to, methylthio, ethylthio, and the like.

(8) The term alkylamino, as used herein, means a NH-alkyl, but not limited to, methylamino, ethylamino, propylamino, 2-propylamino, and the like.

(9) The term alkenyl, as used herein, means a hydrocarbon radical having at least one double bond, which may be in a E- or a Z-arrangement, including, but not limited to, ethenyl, propenyl, 1-butenyl, 2-butenyl and the like.

(10) The term cycloalkyl, as used herein, means a mono- or bicyclic ring, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, norboranyl, adamantyl groups, and the like.

(11) The term alkylene, as used herein, means a linear saturated divalent hydrocarbon radical of one to six carbon atoms or a branched saturated divalent hydrocarbon radical of three to six carbon atoms unless otherwise stated, e.g., methylene, ethylene, propylene, 1-methylpropylene, 2-methylpropylene, butylene, pentylene, and the like.

(12) The term cycloalkylene, as used herein, means a mono- or bicyclic ring, but not limited to, cyclopropylene, cyclobutylene, cyclopentylene, cyclohexylene, cycloheptylene, and the like.

(13) The term aryl, as used herein, means mono- or bi-carbocyclic or mono- or bi-heterocyclic ring which may contain 0 to 4 heteroatoms selected from O, N and S, but not limited to, phenyl, naphthyl, benzofuranyl, benzofurazanyl, benzimidazolonyl, benzoimidazolyl, benzoisothiazolyl, benzoisoxazolyl, benzothiadiazolyl, benzothiazolyl, benzoxadiazolyl, benzoxazolonyl, benzoxazolyl, benzothiophenyl, benzotriazolyl, carbazolyl, carbolinyl, chromanyl, cinnolinyl, 2,3-dioxoindolyl, furanyl, frazanyl, furopyridyl, furopyrrolyl, imidazolyl, imidazopyrazinyl, imidazopyridinyl, imidazopyrimidinyl, imidazothiazolyl, indazolyl, indolazinyl, indolinyl, indolyl, isobenzofuranyl, isochromanyl, isoindolyl, isoquinolyl, isoxazolopyridyl, isoxazolinyl, isoxazolyl, isothiazolyl, naphthyridinyl, oxazolinyl, oxadiazolyl, oxazolyl, oxetanyl, 2-oxoindolyl, phthalazyl, pyrazolopyridyl, pyrazolopyrimidinyl, pyrazolyl, pyrazinyl, pyridyl, pyrimidyl, pyridazinyl, pyridopyrimidinyl, pyrrolopyridyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl, tetrazolopyridyl, tetrazolyl, thiadiazolyl, thiazolyl, thiophenyl, thienopyrazinyl, thienopyrazolyl, thienopyridyl, thienopyrrolyl, triazolopyrimidinyl, triazolyl, 4-oxo-1,4-dihydroquinolyl, 2-oxo-1,2-dihydropyridyl, 4-oxo-1,4-dihydropyrimidyl, 2-oxo-1,2-dihydroquinolyl, 4-oxo-4H-pyrido[1,2-a]pyrimidyl, 4-oxo-1,4-dihydro-1,8-naphthyridyl, and N-oxides thereof.

(14) The term heterocyclic group as used herein includes both unsaturated and saturated heterocyclic moieties, wherein the unsaturated heterocyclic moieties (i.e. heteroaryl) include benzofuranyl, benzofurazanyl, benzimidazolonyl, benzoimidazolyl, benzoisothiazolyl, benzoisoxazolyl, benzothiadiazolyl, benzothiazolyl, benzoxadiazolyl, benzoxazolonyl, benzoxazolyl, benzothiophenyl, benzotriazolyl, carbazolyl, carbolinyl, chromanyl, cinnolinyl, 2,3-dioxoindolyl, furanyl, frazanyl, furopyridyl, furopyrrolyl, imidazolyl, imidazopyrazinyl, imidazopyridinyl, imidazopyrimidinyl, imidazothiazolyl, indazolyl, indolazinyl, indolinyl, indolyl, isobenzofuranyl, isochromanyl, isoindolyl, isoquinolyl, isoxazolopyridyl, isoxazolinyl, isoxazolyl, isothiazolyl, naphthyridinyl, oxazolinyl, oxadiazolyl, oxazolyl, oxetanyl, 2-oxoindolyl, oxoisoindolyl, phthalazyl, pyrazolyl, pyrazolopyridyl, pyrazolopyrimidinyl, pyrazinyl, pyridyl, pyrimidyl, pyridazinyl, pyridopyrimidinyl, pyrrolopyridyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl, tetrazolopyridyl, tetrazolyl, thiadiazoleyl, thiazolyl, thiophenyl, thienopyrazinyl, thienopyrazolyl, thienopyridyl, thienopyrrolyl, triazolopyrimidinyl, triazolyl, 4-oxo-1,4-dihydroquinolyl, 2-oxo-1,2-dihydropyridyl, 4-oxo-1,4-dihydropyrimidyl, 2-oxo-1,2-dihydroquinolyl, 4-oxo-4H-pyrido[1,2-a]pyrimidyl, 4-oxo-1,4-dihydro-1,8-naphthyridyl, and N-oxides thereof, and wherein the saturated heterocyclic moieties include azetidinyl, 1,4-dioxanyl, hexahydroazepinyl, piperazinyl, piperidinyl, pyridin-2-onyl, pyrrolidinyl, morpholinyl, tetrahydrofuranyl, thiomorpholinyl, triazolopyrimidyl, tetrahydrothienyl, 3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazinyl, 2-oxo-2,5,6,7-tetrahydro-1H-cyclopentapyridyl, 4,5,6,7-tetrahydro-indazolyl, 5,6,7,8-tetrahydro-1,6-naphthyridyl, and N-oxides thereof and S-oxides thereof.

(15) The term C.sub.0, as used herein, means direct bond.

(16) The term protecting group, as used herein, means a hydroxy or amino protecting group which is selected from typical hydroxy or amino protecting groups described in Protective Groups in Organic Synthesis edited by T. W. Greene et al. (John Wiley & Sons, 2007).

(17) The terms treating or treatment, as used herein, includes prohibiting, restraining, slowing, stopping, or reversing the progression or severity of an existing symptom or disorder. As used herein, the term preventing or to prevent includes prohibiting, restraining, or inhibiting the incidence or occurrence of a symptom or disorder.

(18) As used herein, the article a or an refers to both the singular and plural form of the object to which it refers unless indicated otherwise.

(19) Included within the scope of the compounds of the invention are all salts, solvates, hydrates, complexes, polymorphs, prodrugs, radiolabeled derivatives, stereoisomers and optical isomers of the compounds of formula (I).

(20) Compounds of formula (I) can form acid addition salts thereof. It will be appreciated that for use in medicine the salts of the compounds of formula (I) should be pharmaceutically acceptable. Suitable pharmaceutically acceptable salts will be apparent to those skilled in the art and include those described in J. Pharm. Sci, 1977, 66, 1-19, such as acid addition salts formed with inorganic acids e.g. hydrochloric, hydrobromic, sulfuric, nitric or phosphoric acid; and organic acids e.g. succinic, maleic, formic, acetic, trifluoroacetic, propionic, fumaric, citric, tartaric, benzoic, p-toluenesulfonic, methanesulfonic or naphthalenesulfonic acid. Certain of the compounds of formula (I) may form acid addition salts with one or more equivalents of the acid. The present invention includes within its scope all possible stoichiometric and non-stoichiometric forms. In addition, certain compounds containing an acidic function such as a carboxy can be isolated in the form of their inorganic salt in which the counter ion can be selected from sodium, potassium, lithium, calcium, magnesium and the like, as well as from organic bases such as triethylamine.

(21) Also within the scope of the invention are so-called prodrugs of the compounds of formula (I). Thus certain derivatives of compounds of formula (I) which may have little or no pharmacological activity themselves can, when administered into or onto the body, be converted into compounds of formula (I) having the desired activity, for example, by hydrolytic or hydrolysis cleavage. Such derivatives are referred to as prodrugs. Further information on the use of prodrugs may be found in Pro-drugs as Novel Delivery Systems, Vol. 14, ACS Symposium Series (T Higuchi and W Stella) and Bioreversible Carriers in Drug Design, Pergamon Press, 1987 (ed. E B Roche, American Pharmaceutical Association).

(22) The term animal, as used herein, includes a mammalian subject or a non-mammalian subject. Examples of suitable mammalian subject may include, without limit, human, rodents, companion animals, livestock, and primates. Suitable rodents may include, but are not limited to, mice, rats, hamsters, gerbils, and guinea pigs. Suitable companion animals may include, but are not limited to, cats, dogs, rabbits, and ferrets. Suitable livestock may include, but are not limited to, horses, goats, sheep, swine, cattle, llamas, and alpacas. Suitable primates may include, but are not limited to, chimpanzees, lemurs, macaques, marmosets, spider monkeys, squirrel monkeys, and vervet monkeys. Examples of suitable non-mammalian subject may include, without limit, birds, reptiles, amphibians, and fish. Non-limiting examples of birds include chickens, turkeys, ducks, and geese. The preferred mammalian subject is a human.

(23) Prodrugs in accordance with the invention can, for example, be produced by replacing appropriate functionalities present in the compounds of formula (I) with certain moieties known to those skilled in the art as pro-moieties as described, for example, in Design of Prodrugs by H Bundgaard (Elsevier, 1985). Some examples of prodrugs in accordance with the invention include:

(24) (i) where the compound of formula (I) contains an alcohol functionality (OH), compounds wherein the hydroxy group is replaced with a moiety convertible in vivo into the hydroxy group. Said moiety convertible in vivo into the hydroxy group means a moiety transformable in vivo into a hydroxyl group by e.g. hydrolysis and/or by an enzyme, e.g. an esterase. Examples of said moiety include, but are not limited to, ester and ether groups which may be hydrolyzed easily in vivo. Preferred are the moieties replaced the hydrogen of hydroxy group with acyloxyalkyl, 1-(alkoxycarbonyloxy)alkyl, phthalidyl and acyloxyalkyloxycarbonyl such as pivaloyloxymethyloxycarbonyl, and

(25) (ii) where the compound of the formula (I) contains an amino group, an amide derivative prepared by reacting with a suitable acid halide or a suitable acid anhydride is exemplified as a prodrug. A particularly preferred amide derivative as a prodrug is NHCO(CH.sub.2).sub.2OCH.sub.3, NHCOCH(NH.sub.2)CH.sub.3 or the like.

(26) Further examples of replacement groups in accordance with the foregoing examples and examples of other prodrug types may be found in the aforementioned references.

(27) Compounds of formula (I) and salts thereof may be prepared in crystalline or non-crystalline form, and, if crystalline, may optionally be hydrated or solvated. This invention includes within its scope stoichiometric hydrates or solvates as well as compounds containing variable amounts of water and/or solvent.

(28) Salts and solvates having non-pharmaceutically acceptable counter-ions or associated solvents are within the scope of the present invention, for example, for use as intermediates in the preparation of other compounds of formula (I) and their pharmaceutically acceptable salts.

(29) Compounds of formula (I) may have polymorphs in crystalline form, which are within the scope of the present invention.

(30) Additionally, compounds of formula (I) may be administered as prodrugs. As used herein, a prodrug of a compound of formula (I) is a functional derivative of the compound which, upon administration to a patient, eventually liberates the compound of formula (I) in vivo. Administration of a compound of formula (I) as a prodrug may enable the skilled artisan to do one or more of the following: (a) modify the onset of action of the compound in vivo; (b) modify the duration of action of the compound in vivo; (c) modify the transportation or distribution of the compound in vivo; (d) modify the solubility of the compound in vivo; and (e) overcome a side effect or other difficulty encountered with the compound. Typical functional derivatives used to prepare prodrugs include modifications of the compound that are chemically or enzymatically cleaved in vivo. Such modifications, which include the preparation of phosphates, amides, esters, thioesters, carbonates, and carbamates, are well known to those skilled in the art.

(31) In certain of the compounds of formula (I), there may be one or more chiral carbon atoms. In such cases, compounds of formula (I) exist as stereoisomers. The invention extends to all optical isomers such as stereoisomeric forms of the compounds of formula (I) including enantiomers, diastereoisomers and mixtures thereof, such as racemates. The different stereoisomeric forms may be separated or resolved one from the other by conventional methods or any given isomer may be obtained by conventional stereoselective or asymmetric syntheses.

(32) Certain of the compounds herein can exist in various tautomeric forms and it is to be understood that the invention encompasses all such tautomeric forms.

(33) The invention also includes isotopically-labeled compounds, which are identical to those described herein, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, iodine, and chlorine, such as .sup.2H, .sup.3H, .sup.11C, .sup.13C, .sup.14C, .sup.18F, .sup.123I and .sup.125I. Compounds of the invention that contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of the present invention. Isotopically-labeled compounds of the present invention, for example those into which radioactive isotopes such as .sup.3H, .sup.14C are incorporated, are useful in drug and/or substrate tissue distribution assays. Tritiated, i.e., .sup.3H, and carbon-14, i.e., .sup.14C, isotopes are particularly preferred for their ease of preparation and detectability. .sup.11C and .sup.18F isotopes are particularly useful in PET (positron emission tomography), and .sup.123I isotopes are particularly useful in SPECT (single photon emission computerized tomography), all useful in brain imaging. Further, substitution with heavier isotopes such as deuterium, i.e., .sup.2H, can afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements and, hence, may be preferred in some circumstances. Isotopically labeled compounds of the invention can generally be prepared by carrying out the procedures disclosed in the Schemes and/or in the Examples below, then substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.

(34) With respect to other compounds disclosed in the art, certain compounds exhibit unexpected properties, such as with respect to duration of action and/or metabolism, such as increased metabolic stability, enhanced oral bioavailability or absorption, and/or decreased drug-drug interactions.

(35) The compounds of formula (I), being Na.sub.v1.3 and/or Na.sub.v1.7 channel blockers, are potentially useful in the treatment of a range of disorders. The treatment of pain, particularly chronic, inflammatory, neuropathic, nociceptive and visceral pain, is a preferred use.

(36) Physiological pain is an important protective mechanism designed to warn of danger from potentially injurious stimuli from the external environment. The system operates through a specific set of primary sensory neurones and is activated by noxious stimuli via peripheral transducing mechanisms (see Millan, 1999, Prog. Neurobiol., 57, 1-164 for a review). These sensory fibres are known as nociceptors and are characteristically small diameter axons with slow conduction velocities. Nociceptors encode the intensity, duration and quality of noxious stimulus and by virtue of their topographically organised projection to the spinal cord, the location of the stimulus. The nociceptors are found on nociceptive nerve fibres of which there are two main types, A- fibres (myelinated) and C fibres (non-myelinated). The symbol is written delta hereafter. The activity generated by nociceptor input is transferred, after complex processing in the dorsal horn, either directly, or via brain stem relay nuclei, to the ventrobasal thalamus and then on to the cortex, where the sensation of pain is generated.

(37) Pain may generally be classified as acute or chronic. Acute pain begins suddenly and is short-lived (usually in twelve weeks or less). It is usually associated with a specific cause such as a specific injury and is often sharp and severe. It is the kind of pain that can occur after specific injuries resulting from surgery, dental work, a strain or a sprain. Acute pain does not generally result in any persistent psychological response. In contrast, chronic pain is long-term pain, typically persisting for more than three months and leading to significant psychological and emotional problems. Common examples of chronic pain are neuropathic pain (e.g. painful diabetic neuropathy, postherpetic neuralgia), carpal tunnel syndrome, back pain, headache, cancer pain, arthritic pain and chronic post-surgical pain.

(38) When a substantial injury occurs to body tissue, via disease or trauma, the characteristics of nociceptor activation are altered and there is sensitisation in the periphery, locally around the injury and centrally where the nociceptors terminate. These effects lead to a heightened sensation of pain. In acute pain these mechanisms can be useful, in promoting protective behaviours which may better enable repair processes to take place. The normal expectation would be that sensitivity returns to normal once the injury has healed. However, in many chronic pain states, the hypersensitivity far outlasts the healing process and is often due to nervous system injury. This injury often leads to abnormalities in sensory nerve fibres associated with maladaptation and aberrant activity (Woolf & Salter, 2000, Science, 288, 1765-1768).

(39) Clinical pain is present when discomfort and abnormal sensitivity feature among the patient's symptoms. Patients tend to be quite heterogeneous and may present with various pain symptoms. Such symptoms include: 1) spontaneous pain which may be dull, burning, or stabbing; 2) exaggerated pain responses to noxious stimuli (hyperalgesia); and 3) pain produced by normally innocuous stimuli (allodyniaMeyer et al., 1994, Textbook of Pain, 13-44). Although patients suffering from various forms of acute and chronic pain may have similar symptoms, the underlying mechanisms may be different and may, therefore, require different treatment strategies. Pain can also therefore be divided into a number of different subtypes according to differing pathophysiology, including nociceptive, inflammatory and neuropathic pain.

(40) Nociceptive pain is induced by tissue injury or by intense stimuli with the potential to cause injury. Pain afferents are activated by transduction of stimuli by nociceptors at the site of injury and activate neurons in the spinal cord at the level of their termination. This is then relayed up the spinal tracts to the brain where pain is perceived (Meyer et al., 1994, Textbook of Pain, 13-44). The activation of nociceptors activates two types of afferent nerve fibres. Myelinated A-delta fibres transmit rapidly and are responsible for sharp and stabbing pain sensations, whilst unmyelinated C fibres transmit at a slower rate and convey a dull or aching pain. Moderate to severe acute nociceptive pain is a prominent feature of pain from central nervous system trauma, strains/sprains, burns, myocardial infarction and acute pancreatitis, post-operative pain (pain following any type of surgical procedure), posttraumatic pain, renal colic, cancer pain and back pain. Cancer pain may be chronic pain such as tumour related pain (e.g. bone pain, headache, facial pain or visceral pain) or pain associated with cancer therapy (e.g. postchemotherapy syndrome, chronic postsurgical pain syndrome or post radiation syndrome). Cancer pain may also occur in response to chemotherapy, immunotherapy, hormonal therapy or radiotherapy. Back pain may be due to herniated or ruptured intervertebral discs or abnormalities of the lumbar facet joints, sacroiliac joints, paraspinal muscles or the posterior longitudinal ligament. Back pain may resolve naturally but in some patients, where it lasts over 12 weeks, it becomes a chronic condition which can be particularly debilitating.

(41) Neuropathic pain is currently defined as pain initiated or caused by a primary lesion or dysfunction in the nervous system. Nerve damage can be caused by trauma and disease and thus the term neuropathic pain encompasses many disorders with diverse aetiologies. These include, but are not limited to, peripheral neuropathy, diabetic neuropathy, post herpetic neuralgia, trigeminal neuralgia, back pain, cancer neuropathy, HIV neuropathy, phantom limb pain, carpal tunnel syndrome, central post-stroke pain and pain associated with chronic alcoholism, hypothyroidism, uremia, multiple sclerosis, spinal cord injury, Parkinson's disease, epilepsy and vitamin deficiency. Neuropathic pain is pathological as it has no protective role. It is often present well after the original cause has dissipated, commonly lasting for years, significantly decreasing a patient's quality of life (Woolf and Mannion, 1999, Lancet, 353, 1959-1964). The symptoms of neuropathic pain are difficult to treat, as they are often heterogeneous even between patients with the same disease (Woolf & Decosterd, 1999, Pain Supp., 6, S141-S147; Woolf and Mannion, 1999, Lancet, 353, 1959-1964). They include spontaneous pain, which can be continuous, and paroxysmal or abnormal evoked pain, such as hyperalgesia (increased sensitivity to a noxious stimulus) and allodynia (sensitivity to a normally innocuous stimulus).

(42) The inflammatory process is a complex series of biochemical and cellular events, activated in response to tissue injury or the presence of foreign substances, which results in swelling and pain (Levine and Taiwo, 1994, Textbook of Pain, 45-56). Arthritic pain is the most common inflammatory pain. Rheumatoid disease is one of the commonest chronic inflammatory conditions in developed countries and rheumatoid arthritis is a common cause of disability. The exact aetiology of rheumatoid arthritis is unknown, but current hypotheses suggest that both genetic and microbiological factors may be important (Grennan & Jayson, 1994, Textbook of Pain, 397-407). It has been estimated that almost 16 million Americans have symptomatic osteoarthritis (OA) or degenerative joint disease, most of whom are over 60 years of age, and this is expected to increase to 40 million as the age of the population increases, making this a public health problem of enormous magnitude (Houge & Mersfelder, 2002, Ann Pharmacother., 36, 679-686; McCarthy et al., 1994, Textbook of Pain, 387-395). Most patients with osteoarthritis seek medical attention because of the associated pain. Arthritis has a significant impact on psychosocial and physical function and is known to be the leading cause of disability in later life. Ankylosing spondylitis is also a rheumatic disease that causes arthritis of the spine and sacroiliac joints. It varies from intermittent episodes of back pain that occur throughout life to a severe chronic disease that attacks the spine, peripheral joints and other body organs.

(43) Another type of inflammatory pain is visceral pain which includes pain associated with inflammatory bowel disease (IBD). Visceral pain is pain associated with the viscera, which encompass the organs of the abdominal cavity. These organs include the sex organs, spleen and part of the digestive system. Pain associated with the viscera can be divided into digestive visceral pain and non-digestive visceral pain. Commonly encountered gastrointestinal (GI) disorders that cause pain include functional bowel disorder (FBD) and inflammatory bowel disease (IBD). These GI disorders include a wide range of disease states that are currently only moderately controlled, including, in respect of FBD, gastroesophageal reflux, dyspepsia, irritable bowel syndrome (IBS) and functional abdominal pain syndrome (FAPS), and, in respect of IBD, Crohn's disease, ileitis and ulcerative colitis, all of which regularly produce visceral pain. Other types of visceral pain include the pain associated with dysmenorrhea, cystitis and pancreatitis and pelvic pain.

(44) It should be noted that some types of pain have multiple aetiologies and thus can be classified in more than one area, e.g. back pain and cancer pain have both nociceptive and neuropathic components.

(45) Other types of pain include:

(46) (i) pain resulting from musculo-skeletal disorders, including myalgia, fibromyalgia, spondylitis, seronegative (non-rheumatoid) arthropathies, non-articular rheumatism, dystrophinopathy, glycogenolysis, polymyositis and pyomyositis;

(47) (ii) heart and vascular pain, including pain caused by angina, myocardial infarction, mitral stenosis, pericarditis, Raynaud's phenomenon, scleredema and skeletal muscle ischemia;

(48) (iii) head pain, such as migraine (including migraine with aura and migraine without aura), cluster headache, tension-type headache, mixed headache and headache associated with vascular disorders; and

(49) (vi) orofacial pain, including dental pain, otic pain, burning mouth syndrome and temporomandibular myofascial pain.

(50) Compounds of formula (I) are also expected to be useful in the treatment of multiple sclerosis.

(51) The invention also relates to therapeutic use of compounds of formula (I) as agents for treating or relieving the symptoms of neurodegenerative disorders. Such neurodegenerative disorders include, for example, Alzheimer's disease, Huntington's disease, Parkinson's disease, and Amyotrophic Lateral Sclerosis. The present invention also covers treating neurodegenerative disorders termed acute brain injury. These include but are not limited to: stroke, head trauma, and asphyxia. Stroke refers to a cerebral vascular disease and may also be referred to as a cerebral vascular accident (CVA) and includes acute thromboembolic stroke. Stroke includes both focal and global ischemia. Also, included are transient cerebral ischemic attacks and other cerebral vascular problems accompanied by cerebral ischemia. These vascular disorders may occur in a patient undergoing carotid endarterectomy specifically or other cerebrovascular or vascular surgical procedures in general, or diagnostic vascular procedures including cerebral angiography and the like. Other incidents are head trauma, spinal cord trauma, or injury from general anoxia, hypoxia, hypoglycemia, hypotension as well as similar injuries seen during procedures from emboly, hyperfusion, and hypoxia. The instant invention would be useful in a range of incidents, for example, during cardiac bypass surgery, in incidents of intracranial hemorrhage, in perinatal asphyxia, in cardiac arrest, and status epilepticus.

(52) A skilled physician will be able to determine the appropriate situation in which subjects are susceptible to or at risk of, for example, stroke as well as suffering from stroke for administration by methods of the present invention.

(53) TTX-S sodium channels have been implicated in a wide range of biological functions. This has suggested a potential role for these receptors in a variety of disease processes in humans or other species. The compounds of the present invention have utility in treating, preventing, ameliorating, controlling or reducing the risk of a variety of neurological and psychiatric disorders associated with TTX-S sodium channels, including one or more of the following conditions or diseases: pain, acute pain, chronic pain, neuropathic pain, inflammatory pain, visceral pain, nociceptive pain, multiple sclerosis, neurodegenerative disorder, irritable bowel syndrome, osteoarthritis, rheumatoid arthritis, neuropathological disorders, functional bowel disorders, inflammatory bowel diseases, pain associated with dysmenorrhea, pelvic pain, cystitis, pancreatitis, migraine, cluster and tension headaches, diabetic neuropathy, peripheral neuropathic pain, sciatica, fibromyalgia Crohn's disease, epilepsy or epileptic conditions, bipolar depression, tachyarrhythmias, mood disorder, bipolar disorder, psychiatric disorders such as anxiety and depression, myotonia, arrhythmia, movement disorders, neuroendocrine disorders, ataxia, incontinence, visceral pain, trigeminal neuralgia, herpetic neuralgia, general neuralgia, postherpetic neuralgia, radicular pain, sciatica, back pain, head or neck pain, severe or intractable pain, breakthrough pain, postsurgical pain, stroke, cancer pain, seizure disorder, causalgia, and chemo-induced pain.

(54) The dosage of active ingredient in the compositions of this invention may be varied, however, it is necessary that the amount of the active ingredient be such that a suitable dosage form is obtained. The active ingredient may be administered to patients (animals and human) in need of such treatment in dosages that will provide optimal pharmaceutical efficacy.

(55) The selected dosage depends upon the desired therapeutic effect, on the route of administration, and on the duration of the treatment. The dose will vary from patient to patient depending upon the nature and severity of disease, the patient's weight, special diets then being followed by a patient, concurrent medication, and other factors which those skilled in the art will recognize.

(56) For administration to human patients, the total daily dose of the compounds of the invention is typically in the range 0.1 mg to 1000 mg depending, of course, on the mode of administration. For example, oral administration may require a total daily dose of from 1 mg to 1000 mg, while an intravenous dose may only require from 0.1 mg to 100 mg. The total daily dose may be administered in single or divided doses and may, at the physician's discretion, fall outside of the typical range given herein.

(57) These dosages are based on an average human subject having a weight of about 60 kg to 70 kg. The physician will readily be able to determine doses for subjects whose weight falls outside this range, such as infants and the elderly.

(58) In one embodiment, the dosage range will be about 0.5 mg to 500 mg per patient per day; in another embodiment about 0.5 mg to 200 mg per patient per day; in another embodiment about 1 mg to 100 mg per patient per day; and in another embodiment about 5 mg to 50 mg per patient per day; in yet another embodiment about 1 mg to 30 mg per patient per day. Pharmaceutical compositions of the present invention may be provided in a solid dosage formulation such as comprising about 0.5 mg to 500 mg active ingredient, or comprising about 1 mg to 250 mg active ingredient. The pharmaceutical composition may be provided in a solid dosage formulation comprising about 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg or 250 mg active ingredient. For oral administration, the compositions may be provided in the form of tablets containing 1.0 to 1000 milligrams of the active ingredient, such as 1, 5, 10, 15, 20, 25, 50, 75, 100, 150, 200, 250, 300, 400, 500, 600, 750, 800, 900, and 1000 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. The compounds may be administered on a regimen of 1 to 4 times per day, such as once or twice per day.

(59) Compounds of the present invention may be used in combination with one or more other drugs in the treatment, prevention, control, amelioration, or reduction of risk of diseases or conditions for which compounds of the present invention or the other drugs may have utility, where the combination of the drugs together are safer or more effective than either drug alone. Such other drug(s) may be administered, by a route and in an amount commonly used therefore, contemporaneously or sequentially with a compound of the present invention. When a compound of the present invention is used contemporaneously with one or more other drugs, a pharmaceutical composition in unit dosage form containing such other drugs and the compound of the present invention is envisioned. However, the combination therapy may also include therapies in which the compound of the present invention and one or more other drugs are administered on different overlapping schedules. It is also contemplated that when used in combination with one or more other active ingredients, the compounds of the present invention and the other active ingredients may be used in lower doses than when each is used singly.

(60) Accordingly, the pharmaceutical compositions of the present invention include those that contain one or more other active ingredients, in addition to a compound of the present invention. The above combinations include combinations of a compound of the present invention not only with one other active compound, but also with two or more other active compounds.

(61) Likewise, compounds of the present invention may be used in combination with other drugs that are used in the prevention, treatment, control, amelioration, or reduction of risk of the diseases or conditions for which compounds of the present invention are useful. Such other drugs may be administered, by a route and in an amount commonly used therefore, contemporaneously or sequentially with a compound of the present invention. When a compound of the present invention is used contemporaneously with one or more other drugs, a pharmaceutical composition containing such other drugs in addition to the compound of the present invention is envisioned. Accordingly, the pharmaceutical compositions of the present invention include those that also contain one or more other active ingredients, in addition to a compound of the present invention.

(62) The weight ratio of the compound of the compound of the present invention to the second active ingredient may be varied and will depend upon the effective dose of each ingredient. Generally, an effective dose of each will be used. Thus, for example, when a compound of the present invention is combined with another agent, the weight ratio of the compound of the present invention to the other agent will generally range from about 1000:1 to about 1:1000, including about 200:1 to about 1:200. Combinations of a compound of the present invention and other active ingredients will generally also be within the aforementioned range, but in each case, an effective dose of each active ingredient should be used. In such combinations the compound of the present invention and other active agents may be administered separately or in conjunction. In addition, the administration of one element may be prior to, concurrent to, or subsequent to the administration of other agent(s).

(63) A TTX-S sodium channels blocker may be usefully combined with another pharmacologically active compound, or with two or more other pharmacologically active compounds, particularly in the treatment of inflammatory, pain and urological diseases or disorders. For example, a TTX-S sodium channels blocker, particularly a compound of formula (I), or a prodrug thereof or a pharmaceutically acceptable salt or solvate thereof, as defined above, may be administered simultaneously, sequentially or separately in combination with one or more agents selected from an opioid analgesic, e.g. morphine, heroin, hydromorphone, oxymorphone, levorphanol, levallorphan, methadone, meperidine, fentanyl, cocaine, codeine, dihydrocodeine, oxycodone, hydrocodone, propoxyphene, nalmefene, nalorphine, naloxone, naltrexone, buprenorphine, butorphanol, nalbuphine or pentazocine; a nonsteroidal antiinflammatory drug (NSAID), e.g. aspirin, diclofenac, diflusinal, etodolac, fenbufen, fenoprofen, flufenisal, flurbiprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, meclofenamic acid, mefenamic acid, meloxicam, nabumetone, naproxen, nimesulide, nitroflurbiprofen, olsalazine, oxaprozin, phenylbutazone, piroxicam, sulfasalazine, sulindac, tolmetin or zomepirac; a barbiturate sedative, e.g. amobarbital, aprobarbital, butabarbital, butabital, mephobarbital, metharbital, methohexital, pentobarbital, phenobartital, secobarbital, talbutal, theamylal or thiopental; a benzodiazepine having a sedative action, e.g. chlordiazepoxide, clorazepate, diazepam, flurazepam, lorazepam, oxazepam, temazepam or triazolam; an H1 antagonist having a sedative action, e.g. diphenhydramine, pyrilamine, promethazine, chlorpheniramine or chlorcyclizine; a sedative such as glutethimide, meprobamate, methaqualone or dichloralphenazone; a skeletal muscle relaxant, e.g. baclofen, carisoprodol, chlorzoxazone, cyclobenzaprine, methocarbamol or orphrenadine; an NMDA receptor antagonist, e.g. dextromethorphan ((+)-3-hydroxy-N-methylmorphinan) or its metabolite dextrorphan ((+)-3-hydroxy-N-methylmorphinan), ketamine, memantine, pyrroloquinoline quinine, cis-4-(phosphonomethyl)-2-piperidinecarboxylic acid, budipine, EN-3231 (MorphiDex, a combination formulation of morphine and dextromethorphan), topiramate, neramexane or perzinfotel including an NR2B antagonist, e.g. ifenprodil, traxoprodil or ()-(R)-6-{2-[4-(3-fluorophenyl)-4-hydroxy-1-piperidinyl]-1-hydroxyethyl-3,4-dihydro-2(1H)-quinolinone; an alpha-adrenergic, e.g. doxazosin, tamsulosin, clonidine, guanfacine, dexmedetomidine, modafinil, or 4-amino-6,7-dimethoxy-2-(5-methanesulfonamido-1,2,3,4-tetrahydroisoquinol-2-yl)-5-(2-pyridyl)quinazoline; a tricyclic antidepressant, e.g. desipramine, imipramine, amitriptyline or nortriptyline; an anticonvulsant, e.g. carbamazepine, lamotrigine, topiratmate or valproate; a tachykinin (NK) antagonist, particularly an NK-3, NK-2 or NK-1 antagonist, e.g. alphaR,9R)-7-[3,5-bis(trifluoromethyl)benzyl]-8,9,10,11-tetrahydro-9-methyl-5-(4-methylphenyl)-7H-[1,4]diazocino[2,1-g][1,7]naphthyridine-6,3-dione (TAK-637), 5-[[(2R,3S)-2-[(1R)-1-[3,5-bis(trifluoromethyl)phenyl]ethoxy-3-(4-fluorophenyl)-4-morpholinyl]methyl]-1,2-dihydro-3H-1,2,4-triazol-3-one (MK-869), aprepitant, lanepitant, dapitant or 3-[[2-methoxy-5-(trifluoromethoxy)phenyl]methylamino]-2-phenylpiperidine (2S,3S); a muscarinic antagonist, e.g. oxybutynin, tolterodine, propiverine, trospium chloride, darifenacin, solifenacin, temiverine and ipratropium; a COX-2 selective inhibitor, e.g. celecoxib, rofecoxib, parecoxib, valdecoxib, deracoxib, etoricoxib, or lumiracoxib; a coal-tar analgesic, in particular paracetamol; a neuroleptic such as droperidol, chlorpromazine, haloperidol, perphenazine, thioridazine, mesoridazine, trifluoperazine, fluphenazine, clozapine, olanzapine, risperidone, ziprasidone, quetiapine, sertindole, aripiprazole, sonepiprazole, blonanserin, iloperidone, perospirone, raclopride, zotepine, bifeprunox, asenapine, lurasidone, amisulpride, balaperidone, palindore, eplivanserin, osanetant, rimonabant, meclinertant, Miraxion or sarizotan; a vanilloid receptor agonist (e.g. resiniferatoxin) or antagonist (e.g. capsazepine); a transient receptor potential cation channel subtype (V1, V2, V3, V4, M8, M2, A1) agonist or antagonist; a beta-adrenergic such as propranolol; a local anaesthetic such as mexiletine; a corticosteroid such as dexamethasone; a 5-HT receptor agonist or antagonist, particularly a 5-HT1B/1D agonist such as eletriptan, sumatriptan, naratriptan, zolmitriptan or rizatriptan; a 5-HT2A receptor antagonist such as R(+)-alpha-(2,3-dimethoxy-phenyl)-1-[2-(4-fluorophenylethyl)]-4-piperidinemethanol (MDL-100907); a cholinergic (nicotinic) analgesic, such as ispronicline (TC-1734), (E)-N-methyl-4-(3-pyridinyl)-3-buten-1-amine (RJR-2403), (R)-5-(2-azetidinylmethoxy)-2-chloropyridine (ABT-594) or nicotine; Tramadol; a PDEV inhibitor, such as 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulphonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (sildenafil), (6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxyphenyl)pyrazino[2,1:6,1]pyrido[3,4-b]indole-1,4-dione (IC-351 or tadalafil), 2-[2-ethoxy-5-(4-ethyl-piperazin-1-yl-sulphonyl)phenyl]-5-methyl-7-propyl-3H-imidazo[5,1-f][1,2,4]triazin-4-one (vardenafil), 5-(5-acetyl-2-butoxy-3-pyridinyl)-3-ethyl-2-(1-ethyl-3-azetidinyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one, 5-(5-acetyl-2-propoxy-3-pyridinyl)-3-ethyl-2-(1-isopropyl-3-azetidinyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one, 5-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulphonyl)pyridin-3-yl]-3-ethyl-2-[2-methoxyethyl]-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one, 4-[(3-chloro-4-methoxybenzyl)amino]-2-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-N-(pyrimidin-2-ylmethyl)pyrimidine-5-carboxamide, 3-(1-methyl-7-oxo-3-propyl-6,7-dihydro-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-N-[2-(1-methylpyrrolidin-2-yl)ethyl]-4-propoxybenzenesulfonamide; an alpha-2-delta ligand such as gabapentin, pregabalin, 3-methylgabapentin, (3-(aminomethyl)bicyclo[3.2.0]hept-3-yl)acetic acid, (3S,5R)-3-(aminomethyl)-5-methylheptanoic acid, (3S,5R)-3-amino-5-methylheptanoic acid, (3S,5R)-3-amino-5-methyloctanoic acid, (2S,4S)-4-(3-chlorophenoxy)proline, (2S,4S)-4-(3-fluorobenzyl)proline, [(1R,5R,6S)-6-(aminomethyl)bicyclo[3.2.0]hept-6-yl]acetic acid, 3-((1-(aminomethyl)cyclohexyl)methyl)-4H-[1,2,4]oxadiazol-5-one, C-[1-((1H-tetrazol-5-yl)methyl)cycloheptyl]methylamine, (3S,4S)-(1-(aminomethyl)-3,4-dimethylcyclopentyl)acetic acid, (3S,5R)-3-(aminomethyl)-5-methyloctanoic acid, (3S,5R)-3-amino-5-methylnonanoic acid, (3S,5R)-3-amino-5-methyloctanoic acid, (3R,4R,5R)-3-amino-4,5-dimethylheptanoic acid, and (3R,4R,5R)-3-amino-4,5-dimethyloctanoic acid; a cannabinoid; a metabotropic glutamate subtype 1 receptor (mGluR1) antagonist; a serotonin reuptake inhibitor such as sertraline, sertraline metabolite demethylsertraline, fluoxetine, norfluoxetine (fluoxetine desmethyl metabolite), fluvoxamine, paroxetine, citalopram, citalopram metabolite desmethylcitalopram, escitalopram, d,l-fenfluramine, femoxetine, ifoxetine, cyanodothiepin, litoxetine, dapoxetine, nefazodone, cericlamine and trazodone; a noradrenaline (norepinephrine) reuptake inhibitor, such as maprotiline, lofepramine, mirtazapine, oxaprotiline, fezolamine, tomoxetine, mianserin, buproprion, buproprion metabolite hydroxybuproprion, nomifensine and viloxazine (Vivalan) especially a selective noradrenaline reuptake inhibitor such as reboxetine, in particular (S,S)-reboxetine; a dual serotonin-noradrenaline reuptake inhibitor, such as venlafaxine, venlafaxine metabolite O-desmethylvenlafaxine, clomipramine, clomipramine metabolite desmethylclomipramine, duloxetine, milnacipran and imipramine; an inducible nitric oxide synthase (iNOS) inhibitor such as S-[2-[(1-iminoethyl)amino]ethyl]-L-homocysteine, S-[2-[(1-iminoethyl)-amino]ethyl]-4,4-dioxo-L-cysteine, S-[2-[(1-iminoethyl)amino]ethyl]-2-methyl-L-cysteine, (2S,5Z)-2-amino-2-methyl-7-[(1-iminoethyl)amino]-5-heptenoic acid, 2-[[(1R,3S)-3-amino-4-hydroxy-1-(5-thiazolyl)-butyl]thio]-5-chloro-3-pyridinecarbonitrile; 2-[[(1R,3S)-3-amino-4-hydroxy-1-(5-thiazolyl)butyl]thio]-4-chlorobenzonitrile, (2S,4R)-2-amino-4-[[2-chloro-5-(trifluoromethyl)phenyl]thio]-5-thiazolebutanol, 2-[[(1R,3S)-3-amino-4-hydroxy-1-(5-thiazolyl)butyl]thio]-6-(trifluoromethyl)-3 pyridinecarbonitrile, 2-[[(1R,3S)-3-amino-4-hydroxy-1-(5-thiazolyl)butyl]thio]-5-chlorobenzonitrile, N-[4-[2-(3-chlorobenzylamino)ethyl]phenyl]thiophene-2-carboxamidine, or guanidinoethyldisulfide; an acetylcholinesterase inhibitor such as donepezil; a prostaglandin E2 subtype 4 (EP4) antagonist such as N-[({2-[4-(2-ethyl-4,6-dimethyl-1H-imidazo[4,5-c]pyridin-1-yl)phenyl]ethyl}amino)carbonyl]-4-methylbenzenesulfonamide or 4-[(1S)-1-({[5-chloro-2-(3-fluorophenoxyl)pyridin-3-yl]carbonyl}amino)ethyl]benzoic acid; a leukotriene B4 antagonist; such as 1-(3-biphenyl-4-ylmethyl-4-hydroxy-chroman-7-yl)cyclopentanecarboxylic acid (CP-105696), 5-[2-(2-Carboxyethyl)-3-[6-(4-methoxyphenyl)-5E-hexenyl]oxyphenoxy]valeric acid (ONO-4057) or DPC-11870, a 5-lipoxygenase inhibitor, such as zileuton, 6-[(3-fluoro-5-[4-methoxy-3,4,5,6-tetrahydro-2H-pyran-4-yl])phenoxymethyl]-1-methyl-2-quinolone (ZD-2138), or 2,3,5-trimethyl-6-(3-pyridylmethyl)-1,4-benzoquinone (CV-6504); a sodium channel blocker, such as lidocaine; a calcium channel blocker, such as ziconotide, zonisamide, mibefradil; a 5-HT3 antagonist, such as ondansetron; a chemotherapy drug such as oxaliplatin, 5-fluorouracil, leukovolin, paclitaxel; a calcitonin gene related peptide (CGRP) antagonist; a bradykinin (BK1 and BK2) antagonist; a voltage gated sodium dependent channel blocker (Na.sub.v1.3, Na.sub.v1.7, Na.sub.v1.8); a voltage dependent calcium channel blocker (N-type, T-type); a P2X (ion channel type ATP receptor) antagonist; an acid-sensing ion channel (ASIC1a, ASIC3) antagonist; an Angiotensin AT2 antagonist; a Chemokine CCR2B receptor antagonist; a Cathepsin (B, S, K) inhibitor; a sigma1 receptor agonist or antagonist;

(64) and the pharmaceutically acceptable salts and solvates thereof.

(65) Such combinations offer significant advantages, including synergistic activity, in therapy.

(66) A pharmaceutical composition of the invention, which may be prepared by admixture, suitably at ambient temperature and atmospheric pressure, is usually adapted for oral, parenteral or rectal administration and, as such, may be in the form of tablets, capsules, oral liquid preparations, powders, granules, lozenges, reconstitutable powders, injectable or infusible solutions or suspensions or suppositories. Orally administrate compositions are generally preferred. Tablets and capsules for oral administration may be in unit dose form, and may contain conventional excipients, such as binding agents (e.g. pregelatinised maize starch, polyvinylpyrrolidone or hydroxypropyl methylcellulose); fillers (e.g. lactose, microcrystalline cellulose or calcium hydrogen phosphate); tabletting lubricants (e.g. magnesium stearate, talc or silica); disintegrants (e.g. potato starch or sodium starch glycollate); and acceptable wetting agents (e.g. sodium lauryl sulphate). The tablets may be coated according to methods well known in normal pharmaceutical practice.

(67) Oral liquid preparations may be in the form of, for example, aqueous or oily suspension, solutions, emulsions, syrups or elixirs, or may be in the form of a dry product for reconstitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents (e.g. sorbitol syrup, cellulose derivatives or hydrogenated edible fats), emulsifying agents (e.g. lecithin or acacia), non-aqueous vehicles (which may include edible oils e.g. almond oil, oily esters, ethyl alcohol or fractionated vegetable oils), preservatives (e.g. methyl or propyl-p-hydroxybenzoates or sorbic acid), and, if desired, conventional flavourings or colorants, buffer salts and sweetening agents as appropriate. Preparations for oral administration may be suitably formulated to give controlled release of the active compound or pharmaceutically acceptable salt thereof.

(68) For parenteral administration, fluid unit dosage forms are prepared utilising a compound of formula (I) or pharmaceutically acceptable salt thereof and a sterile vehicle. Formulations for injection may be presented in unit dosage form e.g. in ampoules or in multi-dose, utilising a compound of formula (I) or pharmaceutically acceptable salt thereof and a sterile vehicle, optionally with an added preservative. The compositions may take such forms as suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents. Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile pyrogen-free water, before use. The compound, depending on the vehicle and concentration used, can be either suspended or dissolved in the vehicle. In preparing solutions, the compound can be dissolved for injection and filter sterilised before filling into a suitable vial or ampoule and sealing. Advantageously, adjuvants such as a local anaesthetic, preservatives and buffering agents are dissolved in the vehicle. To enhance the stability, the composition can be frozen after filling into the vial and the water removed under vacuum. Parenteral suspensions are prepared in substantially the same manner, except that the compound is suspended in the vehicle instead of being dissolved, and sterilisation cannot be accomplished by filtration. The compound can be sterilised by exposure to ethylene oxide before suspension in a sterile vehicle. Advantageously, a surfactant or wetting agent is included in the composition to facilitate uniform distribution of the compound.

(69) Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilising agents, dispersing agents, suspending agents, thickening agents, or colouring agents. Drops may be formulated with an aqueous or non-aqueous base also comprising one or more dispersing agents, stabilising agents, solubilising agents or suspending agents. They may also contain a preservative.

(70) Compounds of formula (I) or pharmaceutically acceptable salts thereof may also be formulated in rectal compositions such as suppositories or retention enemas, e.g. containing conventional suppository bases such as cocoa butter or other glycerides.

(71) Compounds of formula (I) or pharmaceutically acceptable salts may also be formulated as depot preparations. Such long acting formulations may be administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection. Thus, for example, the compounds of formula (I) or pharmaceutically acceptable salts may be formulated with suitable polymeric or hydrophobic materials (for example as an emulsion in an acceptable oil) or ion exchange resins, or as sparingly soluble derivatives, for example, as a sparingly soluble salt.

(72) For intranasal administration, compounds formula (I) or pharmaceutically acceptable salts thereof may be formulated as solutions for administration via a suitable metered or unitary dose device or alternatively as a powder mix with a suitable carrier for administration using a suitable delivery device. Thus compounds of formula (I) or pharmaceutically acceptable salts thereof may be formulated for oral, buccal, parenteral, topical (including ophthalmic and nasal), depot or rectal administration or in a form suitable for administration by inhalation or insufflation (either through the mouth or nose). The compounds of formula (I) and pharmaceutically acceptable salts thereof may be formulated for topical administration in the form of ointments, creams, gels, lotions, pessaries, aerosols or drops (e.g. eye, ear or nose drops). Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents. Ointments for administration to the eye may be manufactured in a sterile manner using sterilized components.

(73) General Synthesis

(74) Throughout the instant application, the following abbreviations are used with the following meanings:

(75) DCM Dichloromethane

(76) DMF N,N-Dimethylformamide

(77) DMA N,N-Dimethylacetamide

(78) DME 1,2-Dimethoxyethane

(79) DMSO Dimethyl sulfoxide

(80) EDC 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Hydrochloride

(81) ESI Electrospray ionization

(82) EtOAc Ethyl acetate

(83) EtOH Ethanol

(84) HOBT 1-Hydroxybenztriazole

(85) HBTU O-(Benzotriazol-1-yl)-N,N,N,N-tetramethyluronium Hexafluorophosphate

(86) HPLC High-Performance Liquid Chromatography

(87) LC Liquid Chromatography

(88) LG Leaving Group

(89) MeCN Acetonitrile

(90) MeOH Methanol

(91) MHz Megahertz

(92) MS Mass Spectrometry

(93) NMR Nuclear Magnetic Resonance

(94) PG Protecting Group

(95) rt room temperature

(96) TFA Trifluoroacetic acid

(97) THF Tetrahydrofuran

(98) TLC Thin Layer Chromatography

(99) tR Retention Time

(100) UV Ultraviolet

(101) The term of base is likewise no particular restriction on the nature of the bases used, and any base commonly used in reactions of this type may equally be used here. Examples of such bases include: alkali metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide, potassium phosphate, and barium hydroxide; alkali metal hydrides, such as lithium hydride, sodium hydride, and potassium hydride; alkali metal alkoxides, such as sodium methoxide, sodium ethoxide, and potassium t-butoxide; alkali metal carbonates, such as lithium carbonate, sodium carbonate, potassium carbonate, and cesium carbonate; alkali metal hydrogencarbonates, such as lithium hydrogencarbonate, sodium hydrogencarbonate, and potassium hydrogencarbonate; amines, such as N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 2,6-di(t-butyl)-4-methylpyridine, quinoline, N,N-dimethylaniline, N,N-diethylaniline, 1,5-diazabicyclo[4.3.0]non-5-ene (DBN), 1,4-diazabicyclo[2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), lutidine, and colidine; alkali metal amides, such as lithium amide, sodium amide, potassium amide, lithium diisopropyl amide, potassium diisopropyl amide, sodium diisopropyl amide, lithium bis(trimethylsilyl)amide and potassium bis(trimethylsilyl)amide. Of these, triethylamine, diisopropylethylamine, DBU, DBN, DABCO, pyridine, lutidine, colidine, sodium carbonate, sodium hydrogencarbonate, sodium hydroxide, potassium carbonate, potassium hydrogencarbonate, potassium hydroxide, potassium phosphate, barium hydroxide, and cesium carbonate are preferred.

(102) The reactions are normally and preferably effected in the presence of inert solvent. There is no particular restriction on the nature of the solvent to be employed, provided that it has no adverse effect on the reaction or the reagents involved and that it can dissolve reagents, at least to some extent. Examples of suitable solvents include, but not limited to: halogenated hydrocarbons, such as dichloromethane, chloroform, carbon tetrachloride, and dichloroethane; ethers, such as diethyl ether, diisopropyl ether, THF, and dioxane; aromatic hydrocarbons, such as benzene, toluene and nitrobenzene; amides, such as, DMF, DMA, and hexamethylphosphoric triamide; amines, such as N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, N,N-dimethylaniline, and N,N-diethylaniline; alcohols, such as methanol, ethanol, propanol, isopropanol, and butanol; nitriles, such as acetonitrile and benzonitrile; sulfoxides, such as DMSO and sulfolane; ketones, such as acetone and diethylketone. Of these solvents, including but not limited to DMF, DMA, DMSO, THF, diethyl ether, diisopropylether, DME, MeCN, DCM, dichloroethane and chloroform are preferred.

EXAMPLES

(103) The invention is illustrated in the following non-limiting examples in which, unless stated otherwise: all reagents are commercially available, all operations are carried out at room or ambient temperature, that is, in the range of about 18-25 C.; evaporation of solvent is carried out using a rotary evaporator under reduced pressure with a bath temperature of up to about 60 C.; reactions are monitored by thin layer chromatography (TLC) and reaction times are given for illustration only; the structure and purity of all isolated compounds are assured by at least one of the following techniques: TLC (Merck silica gel 60 F.sub.254 precoated TLC plates or Merck NH.sub.2 F.sub.254 precoated HPTLC plates), mass spectrometry or NMR. Yields are given for illustrative purposes only. Flash column chromatography is carried out using Merck silica gel 60 (230-400 mesh ASTM), Fuji Silysia Chromatorex (registered trade mark) DU3050 (Amino Type), Wako Wakogel C300-HG, Biotage silica KP-Sil, Yamazen Hi-FLASH column, YMC DispoPack-SIL, or Biotage amino bounded silica KP-NH. The purification of compounds using HPLC (preparative LC-MS) is performed by the following apparatus and conditions.

(104) Apparatus; Waters MS-trigger AutoPurification system

(105) Column; Waters XTerra C18, 1950 mm, 5 micrometer particle

(106) Condition A: Methanol or acetonitrile/0.01% (v/v) ammonia aqueous solution

(107) Condition B: Methanol or acetonitrile/0.05% (v/v) formic acid aqueous solution

(108) Low-resolution mass spectral data (ESI) are obtained by the following apparatus and conditions: Apparatus; Waters Alliance HPLC system on ZQ or ZMD mass spectrometer and UV detector. NMR data are determined at 270 MHz (JEOL JNM-LA 270 spectrometer) or 300 MHz (JEOL JNM-LA300) using deuterated chloroform (99.8% D) or dimethylsulfoxide (99.9% D) as solvent unless indicated otherwise, relative to tetramethylsilane (TMS) as internal standard in parts per million (ppm); conventional abbreviations used are: s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet, br=broad, etc. Chemical symbols have their usual meanings; M (mol(s) per liter), L (liter(s)), mL (milliliter(s)), g (gram(s)), mg (milligram(s)), mol (moles), mmol (millimoles).
Each prepared compound is generally named by ChemBioDraw (Ultra, version 12.0, CambridgeSoft).

(109) Conditions for Determining HPLC Retention Time:

(110) Method:

(111) Apparatus: Waters ACQUITY Ultra Performance LC with TUV Detector and ZQ mass spectrometer

(112) Column: Waters ACQUITY C18, 2.1100 mm, 1.7 micrometer particle size

(113) Column Temperature: 60 C.

(114) Flow rate: 0.7 mL/min

(115) Run time: 3 min

(116) UV detection: 210 nm

(117) MS detection: ESI positive/negative mode

(118) Mobile Phases:

(119) A1: 10 mM Ammonium acetate

(120) B1: acetonitrile

(121) Gradient Program:

(122) TABLE-US-00001 Time (min) A1 (%) B1 (%) 0 95 5 0.1 95 5 1.8 5 95 2.3 95 5

(123) All of the amide derivatives of the formula (I) can be prepared by the procedures described in the general methods presented below or by the specific methods described in the Example synthesis part and Intermediate synthesis part, or by routine modifications thereof. The present invention also encompasses any one or more of these processes for preparing the amide derivatives of formula (I), in addition to any novel intermediates used therein.

(124) In the following general methods, descriptors are as previously defined for the amide derivatives of the formula (I) unless otherwise stated.

(125) ##STR00004##

(126) In Step A, a compound of formula (I) can be prepared from a compound of formula (IV) by amidation with a compound of formula (III) using a suitable condensation agent such as HBTU and EDC-HOBT, preferably under the presence of a base such as triethylamine and N,N-diisopropylethylamine in a suitable solvent such as DMF, DMA and dichloromethane at a temperature of from about 5 to 60 C. for about 1 to 24 hours. In addition, a compound of formula (I) can be also prepared from a compound of formula (IV) by amidation with an acid halide prepared from a compound of formula (III) using thionyl chloride or oxalyl chloride, preferably under the presence of a base such as triethylamine, pyridine, and N,N-diisopropylethylamine in a suitable solvent such as dichloromethane at a temperature of from about 5 to 40 C. for about 1 to 24 hours.

(127) ##STR00005##

(128) In Step B-a, a compound of formula (VI) can be prepared as described in the preparation of a compound of formula (I) in Step A.

(129) Then, a compound of formula (I) can be prepared, in Step B-b, by acylation with a suitable acid halide using a suitable base such as pyridine and a suitable solvent such as DMA at a temperature of from about 5 to 120 C. for about 1 to 24 hours. Examples of suitable acid halide include, but not limited to, acid halides such as acetyl chloride, propionyl chloride, isobutyryl chloride, and cyclopropanecarbonyl chloride.

(130) ##STR00006##

(131) In Step C-a, a compound of formula (VIII) can be prepared as described in the preparation of a compound of formula (I) in Step A.

(132) When a leaving group of formula (VIII), in Step C-b, is such as O-trifluoromethanesulfonate, O-tosylate, O-mesylate, iodide, bromide, and chloride, a compound of formula (I) can be prepared by coupling of a compound of formula (VIII) with a suitable carboxamide under coupling conditions in suitable organic solvents in the presence of a suitable transition metal catalyst and in the presence or absence of a base. Examples of suitable transition metal catalysts include: tetrakis(triphenylphosphine)palladium(0), bis(triphenylphosphine)palladium(ll)chloride, copper(0), copper(l)acetate, copper(l)bromide, copper(l)chloride, copper(l)iodide, copper(l)oxide, copper(ll)trifluoromethanesulfonate, copper(ll)acetate, copper(ll)bromide, copper(ll)chloride, copper(ll)iodide, copper(ll)oxide, copper(ll)trifluoromethanesulfonate, palladium(ll)acetate, palladium(ll)chloride, bis(acetonitrile)dichloropalladium(II), bis(dibenzylideneacetone)palladium(0), tris(dibenzylideneacetone)dipalladium(0) and [1,1-bis(diphenylphosphino)ferrocene]palladium(ll)dichloride. Preferred catalysts are tetrakis(triphenylphosphine)palladium(0), bis(triphenylphosphine)palladium(ll)chloride, palladium(ll) acetate, palladium(ll) chloride, bis(acetonitrile)dichloropalladium(0), bis(dibenzylideneacetone)palladium(0), tris(dibenzylideneacetone)dipalladium(0) and [1,1-bis(diphenylphosphino)ferrocene]palladium(ll)dichloride. Examples of suitable carboxamide include, but not limited to, carboxamides such as acetamide, propionamide, isobutyramide and cyclopropanecarboxamide. Examples of suitable organic solvent include: THF; 1,4-dioxane; DMF; MeCN; alcohols, such as methanol or ethanol; halogenated hydrocarbons, such as DCM, 1,2-dichloroethane, chloroform or carbon tetrachloride; and diethyl ether; in the presence or absence of base such as tripotassium phosphate, sodium bicarbonate, sodium carbonate or potassium carbonate. This reaction can be carried out in the presence of a suitable additive agent. Examples of such additive agents include: 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene, triphenylphosphine, tri-tert-butylphosphine, 1,1-bis(diphenylphosphino)ferrocene, tri-2-furylphosphine, tri-o-tolylphosphine, 2-(dichlorohexylphosphino)biphenyl, triphenylarsine. The reaction can be carried out at a temperature of from about 50 to 200 C., more preferably from about 80 to 170 C. Reaction times are, in general, from about 5 minutes to 48 hrs, more preferably from about 30 minutes to 24 hrs. In an alternative case, the reaction can be carried out with microwave system. The reaction can be carried out at a temperature in the range from about 100 to 200 C., preferably in the range from about 120 to 170 C. Reaction times are, in general, from about 10 minutes to 3 hrs, preferably from about 15 minutes to 1 hr.

(133) ##STR00007##

(134) In Step D, a compound of formula (X) can be prepared from isocyanate of formula (IX) and amine of formula (IV) using a suitable base such as N,N-diisopropylethylamine, triethylamine, and pyridine and a suitable solvent such as DMA, DMF, toluene, THF, and DCM at a temperature of from about 20 to 120 C. for about 1 to 24 hours.

(135) The key intermediate amines of formula (IV) and (VII) can be prepared by the following general synthetic route Scheme E and F.

(136) ##STR00008##

(137) In Step E-a, a compound of formula (XII) can be prepared from acid of the formula (XI) and N,O-dimethylhydroxylamine (Weinreb amide formation) by the method described in Step A.

(138) In Step E-b, a compound of formula (XIII) can be prepared from a compound of formula (XII) by the treatment with a suitable alkyl-metal reagent in an inert solvent. Examples of suitable alkyl-metal reagent include, but not limited to, such as methyllithium, ethyllithium, methylmagnesium chloride, methylmagnesium bromide, methylmagnesium iodide. Examples of inert solvent include, but not limited to, such as THF, DME, and 1,4-dioxane. The reaction can be carried out at a temperature of from about 40 to 100 C., more preferably from about 0 to 50 C. Reaction times are, in general, from about 5 minutes to 48 hrs, more preferably from about 30 minutes to 24 hrs.

(139) In Step E-c, a compound of formula (XIV) can be prepared as a single diastereomer from carbonyl compound of formula (XIII) and a chiral tert-butanesulfinamide by the conventional methods known to those skilled in the art (Pure Appl. Chem., 75, 39-46, 2003; Tetrahedron Lett., 45, 6641-6643, 2004). In the following intermediate and example section, a compound name of formula (XIV) is described as an (R) or (S) isomer, which represents the configuration of a sulfur atom.

(140) In Step E-d, a compound of formula (XV) can be prepared as a single enantiomer from a compound of formula (XIV) by the treatment with acidic condition by the conventional methods known to those skilled in the art (Pure Appl. Chem., 75, 39-46, 2003; Tetrahedron Lett., 45, 6641-6643, 2004).

(141) In Step E-e, a protecting group can be introduced by the conventional methods known to those skilled in the art (typical amino protecting groups described in Protective Groups in Organic Synthesis Forth Edition edited by T. W. Greene et al. (John Wiley & Sons, 2007)).

(142) In Step E-f, a compound of formula (XVII) can be prepared from a compound of the formula (XVI) and a suitable carboxamide by the method described in Step C-b.

(143) In Step E-g, a compound of formula (XVIII) can be prepared by de-protection of a compound of formula (XVII) by the conventional methods known to those skilled in the art (typical amino protecting groups described in Protective Groups in Organic Synthesis Forth Edition edited by T. W. Greene et al. (John Wiley & Sons, 2007)).

(144) When W of key intermediate (IV) or (VII) is C.sub.1-6 alkyl, C.sub.1-6 alkyl group can be introduced by N-alkylation of a compound of formula (XVI) with an alkylating reagent in the presence of a suitable base in an inert solvent. Examples of a suitable base include, but not limited to, such as sodium hydride, potassium carbonate, cesium carbonate, potassium tert-butoxide. Examples of suitable organic solvent include such as THF, 1,4-dioxane, DMF, MeCN, DMA, and toluene. The reaction can be carried out at a temperature of from about 20 to 150 C., more preferably from about 0 to 100 C. Reaction times are, in general, from about 30 minutes to 48 hrs, more preferably from about 30 minutes to 24 hrs.

(145) ##STR00009##

(146) In Step F-a, a compound of formula (XX) can be prepared from a compound of the formula (XIX) and a suitable carboxamide by the method described in Step C-b.

(147) In Step F-b, a compound of formula (XXI) can be prepared by hydrogenation of a compound of formula (XX) under known hydrogenolysis conditions, for example, in the presence of a suitable metal catalyst under a hydrogen atmosphere, or in the presence of hydrogen sources such as formic acid or ammonium formate, in an inert solvent. If desired, the reaction is carried out under acidic conditions, for example, in the presence of hydrochloric acid or acetic acid. A preferred metal catalyst is selected from, for example, nickel catalysts such as Raney nickel, PdC, palladium hydroxide-carbon, platinum oxide, platinum-carbon, ruthenium-carbon, Fe, Zn, Sn, and SnCl.sub.2. Examples of suitable inert aqueous or non-aqueous organic solvents include, but not limited to, alcohols, such as methanol, ethanol or ammonic methanol; ethers, such as THF or 1,4-dioxane; acetone; DMF; halogenated hydrocarbons, such as DCM, 1,2-dichloroethane or chloroform; and acetic acid; or mixtures thereof. The reaction can be carried out at a temperature in the range of from about 20 to 150 C., preferably in the range of from about 20 to 80 C. Reaction times are, in general, from about 10 minutes to 4 days, preferably from about 30 minutes to 24 hrs. This reaction can be carried out under a hydrogen atmosphere at a pressure ranging from about 1 to 100 atms, preferably from about 1 to 5 atms.

(148) All starting materials in the following general syntheses may be commercially available or obtained by the conventional methods known to those skilled in the art, otherwise noted in the intermediate synthesis part.

Intermediate Synthesis Part

(149) <Amine Part>

Amine-1: N-(4-(aminomethyl)pyridin-2-yl)acetamide

: N-(4-cyanopyridin-2-yl)acetamide

(150) A mixture of 2-chloroisonicotinonitrile (1.50 g, 10.8 mmol), acetamide (1.28 g, 21.7 mmol), tris(dibenzylideneacetone)dipalladium(0) (198 mg, 0.22 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (376 mg, 0.65 mmol), and tripotassium phosphate (2.76 g, 13.0 mmol) in dioxane (15 mL) is stirred at 150 C. for 1 hour under microwave irradiation. The resulting mixture is filtered through a pad of Celite, and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (2:1 to 1:2) to give 950 mg (54% yield) of the title compound as a pale yellow solid.

(151) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.52 (1H, s), 8.42 (1H, d, J=5.1 Hz), 8.03 (1H, br s), 7.25 (1H, d, J=5.1 Hz), 2.25 (3H, s), MS (ESI) m/z: 162 (M+H).sup.+.

: N-(4-(aminomethyl)pyridin-2-yl)acetamide

(152) A mixture of N-(4-cyanopyridin-2-yl)acetamide (900 mg, Step-1) and Raney-Nickel (ca 2 mL) in 4 M ammonia solution in MeOH (25 mL) is stirred at rt for 1 hour under a hydrogen atmosphere (1 atm). The mixture is filtered through a pad of Celite, and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on NH-gel eluting with DCM/MeOH (100:1) to give 244 mg (26% yield) of the title compound as a yellow oil.

(153) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.58 (1H, br), 8.20 (1H, d, J=5.1 Hz), 7.04 (1H, d, J=5.1 Hz), 3.91 (2H, s), 2.20 (3H, s), MS (ESI) m/z: 166 (M+H).sup.+.

(154) Amine-2 to 7 are prepared according to the procedure similar to that described in Amine-1, using 2-chloroisonicotinonitrile and appropriate starting materials.

Amine-2: N-(4-(aminomethyl)pyridin-2-yl)propionamide

(155) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.33 (1H, br), 8.20 (1H, d, J=5.1 Hz), 7.03 (1H, d, J=5.1 Hz), 3.91 (2H, s), 2.43 (2H, q, J=8.1 Hz), 1.25 (3H, t, J=8.1 Hz), MS (ESI) m/z: 180 (M+H).sup.+.

Amine-3: N-(4-(aminomethyl)pyridin-2-yl)cyclopropanecarboxamide

(156) MS (ESI) m/z: 192 (M+H).sup.+.

Amine-4: N-(4-(aminomethyl)pyridin-2-yl)benzamide

(157) MS (ESI) m/z: 228 (M+H).sup.+.

Amine-5: N-(4-(aminomethyl)pyridin-2-yl)isobutyramide

(158) MS (ESI) m/z: 194 (M+H).sup.+.

Amine-6: N-(4-(aminomethyl)pyridin-2-yl)cyclobutanecarboxamide

(159) MS (ESI) m/z: 206 (M+H).sup.+.

Amine-7: N-(4-(aminomethyl)-6-methylpyridin-2-yl)propionamide

(160) MS (ESI) m/z: 194 (M+H).sup.+.

Amine-8: N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)acetamide hydrochloride (Single Enantiomer)

: 2-chloro-N-methoxy-N,6-dimethylisonicotinamide

(161) To a mixture of 2-chloro-6-methylisonicotinic acid (2.00 g, 11.7 mmol), N,O-dimethylhydroxylamine hydrochloride (1.19 g, 12.2 mmol), and triethylamine (6.50 mL, 46.6 mmol) in DMF (58 mL), HOBT hydrate (2.68 g, 17.5 mmol) and EDC (3.35 g, 17.5 mmol) are added. After stirring at 60 C. for 2 h, the mixture is poured into water (200 mL). The aqueous layer is extracted with EtOAc-toluene (1:1, 150 mL3). The combined organic layer is washed with water and brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (5:1) to give 2.50 g (93% yield) of the title compound as a colorless oil.

(162) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.36 (1H, s), 7.29 (1H, s), 3.56 (3H, s), 3.36 (3H, s), 2.59 (3H, s), MS (ESI) m/z: 215 (M+H).sup.+.

: 1-(2-chloro-6-methylpyridin-4-yl)ethanone

(163) To a solution of 2-chloro-N-methoxy-N,6-dimethylisonicotinamide (2.50 g, 11.7 mmol, Step-1) in THF (120 mL) is added dropwise a solution of methylmagnesium bromide in THF (0.99 M, 23.5 mL, 23.3 mmol) at 0 C. After stirring at the same temperature, the mixture is poured into water (200 mL), and the aqueous layer is extracted with EtOAc (200 mL2). The combined organic layer is washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 1.90 g (96% yield) of the title compound as a yellow oil. This is used for the next step without purification.

(164) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.57 (1H, s), 7.51 (1H, s), 2.62 (3H, s), 2.60 (3H, s), MS (ESI) m/z: 170 (M+H).sup.+.

: (S)N-(1-(2-chloro-6-methylpyridin-4-yl)ethyl)-2-methylpropane-2-sulfinamide (Single Diastereomer)

(165) A mixture of 1-(2-chloro-6-methylpyridin-4-yl)ethanone (1.90 g, 11.2 mmol, Step-2), (S)-2-methylpropane-2-sulfinamide (1.36 g, 11.2 mmol), and titanium(IV) ethoxide (3.83 g, 16.8 mmol) in THF (60 mL) is refluxed with stirring for 12 hours. After cooling to 0 C., sodium borohydride (848 mg, 22.4 mmol) is added to the mixture. After stirring at rt for 1 h, the reaction is quenched with saturated aqueous sodium bicarbonate solution, and the mixture is diluted with EtOAc and water. The resulting slurry is filtered through a pad of Celite, and the filtrate is extracted with EtOAc. The organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (1:1 to EtOAc only) to give 2.09 g (68% yield) of the title compound as a colorless oil.

(166) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.12 (1H, s), 7.06 (1H, s), 4.50-4.42 (1H, m), 3.44 (1H, d, J=3.7 Hz), 2.54 (3H, s), 1.50 (3H, d, J=6.6 Hz), 1.25 (9H, s), MS (ESI) m/z: 275 (M+H).sup.+.

: 1-(2-chloro-6-methylpyridin-4-yl)ethanamine hydrochloride (Single Enantiomer)

(167) A mixture of (S)N-(1-(2-chloro-6-methylpyridin-4-yl)ethyl)-2-methylpropane-2-sulfinamide (single diastereomer) (2.09 g, 7.61 mmol, Step-3) and 4 M hydrogen chloride in dioxane (10 mL) is stirred at rt for 30 min. After evaporation, the residual solid is washed with diisopropyl ether to give 2.07 g of the title compound as a pale yellow solid. This is used for the next step without further purification.

(168) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.88 (3H, br), 7.54 (1H, s), 7.46 (1H, s), 4.5-4.3 (1H, m), 2.44 (3H, s), 1.48 (3H, d, J=6.6 Hz), MS (ESI) m/z: 171 (M+H).sup.+.

: tert-butyl(1-(2-chloro-6-methylpyridin-4-yl)ethyl)carbamate (Single Enantiomer

(169) To a solution of 1-(2-chloro-6-methylpyridin-4-yl)ethanamine hydrochloride (single enantiomer) (700 mg, 2.87 mmol, Step-4) and triethylamine (1.60 mL, 11.5 mmol), di-tert-butyl dicarbonate (753 mg, 3.45 mmol) is added. After stirring at rt for 1 h, the solvent is removed in vacuo. The residue is poured into saturated aqueous sodium carbonate solution, and the aqueous layer is extracted with EtOAc (twice). The combined organic layer is washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 868 mg of the title compound as a pale yellow solid. This is used for the next step without purification.

(170) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.06 (1H, s), 6.99 (1H, s), 4.82 (1H, br s), 2.52 (3H, s), 1.53 (3H, s), 1.29 (9H, s), MS (ESI) m/z: 271 (M+H).sup.+.

: tert-butyl(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)carbamate (Single Enantiomer)

(171) The title compound is prepared in 82% yield (689 mg, a yellow solid) from tert-butyl(1-(2-chloro-6-methylpyridin-4-yl)ethyl)carbamate (single enantiomer) (850 mg, 2.87 mmol, Step-5) in a similar manner in Step-1 of Amine-1.

(172) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.00 (1H, br s), 7.94 (1H, s), 6.83 (1H, s), 4.90 (1H, brs), 2.42, (3H, s), 2.18 (3H, s), 1.43 (9H, s), 1.40 (3H, s), MS (ESI) m/z: 294 (M+H).sup.+.

: N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)acetamide hydrochloride (Single Enantiomer)

(173) A mixture of tert-butyl(1-(2-acetamido-6-methylpyridin-4-yl)ethyl)carbamate (single enantiomer) (680 mg, 2.15 mmol, Step-6) and 4 M hydrogen chloride in dioxane (10 mL) is stirred at rt for 1 hour. After evaporation of the solvent, diisopropyl ether is added to the residue. The formed solid is collected by filtration to give 572 mg of the title compound as a pale yellow solid.

(174) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 10.9 (1H, brs), 8.85 (3H, brs), 7.97 (1H, s), 7.34 (1H, s), 4.39 (1H, brs), 2.46 (3H, s), 2.13 (3H, s), 1.50 (3H, d, J=6.6 Hz), MS (ESI) m/z: 194 (M+H).sup.+.

(175) Amine-9 to 29 are prepared as a single enantiomer using (S)-2-methylpropane-2-sulfinamide as a chiral auxiliary according to the procedure similar to that described in Amine-8, using the appropriate starting materials and reagents.

Amine-9: N-(4-(1-aminoethyl)pyridin-2-yl)acetamide hydrochloride (Single Enantiomer)

(176) MS (ESI) m/z: 180 (M+H).sup.+.

Amine-10: N-(4-(1-aminoethyl)pyridin-2-yl)propionamide hydrochloride (Single Enantiomer)

(177) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 10.82 (1H, s), 8.70 (2H, br s), 8.36 (1H, d, J=5.1 Hz), 8.15 (1H, s), 7.33 (1H, d, J=5.1 Hz), 4.50-4.36 (1H, m), 2.43 (2H, q, J=7.3 Hz), 1.50 (3H, d, J=6.6 Hz), 1.08 (3H, t, J=7.3 Hz), MS (ESI) m/z: 194 (M+H).sup.+.

Amine-11: N-(4-(1-aminoethyl)pyridin-2-yl)cyclopropanecarboxamide hydrochloride (Single Enantiomer)

(178) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 11.03 (1H, br s), 8.58 (2H, br s), 8.37 (1H, d, J=5.1 Hz), 8.17 (1H, s), 7.26 (1H, d, J=5.1 Hz), 4.48-4.36 (1H, m), 2.21-1.98 (1H, m), 1.48 (3H, d, J=7.0 Hz), 0.87-0.79 (4H, m), MS (ESI) m/z: 206 (M+H).sup.+.

Amine-12: N-(4-(1-aminoethyl)pyridin-2-yl)isobutyramide hydrochloride (Single Enantiomer)

(179) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 11.23 (1H, br s), 8.76 (2H, br s), 8.37 (1H, d, J=5.5 Hz), 8.06 (1H, s), 7.41 (1H, d, J=5.5 Hz), 4.52-4.38 (1H, m), 2.82-2.71 (1H, m), 1.49 (3H, d, J=7.0 Hz), 1.09 (6H, d, J=7.0 Hz), MS (ESI) m/z: 208 (M+H).sup.+.

Amine-13: N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)propionamide hydrochloride (Single Enantiomer)

(180) MS (ESI) m/z: 208 (M+H).sup.+.

Amine-14: N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)isobutyramide hydrochloride (Single Enantiomer)

(181) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 10.64 (1H, s), 8.63 (2H, br s), 8.05 (1H, s), 7.18 (1H, s), 4.42-4.27 (1H, m), 2.77 (1H, septet, J=7.3 Hz), 2.43 (3H, s), 1.48 (3H, d, J=7.3 Hz), 1.09 (6H, d, J=7.3 Hz), MS (ESI) m/z: 222 (M+H).sup.+.

Amine-15: N-(4-(1-aminoethyl)-6-methylpyrimidin-2-yl)isobutyramide hydrochloride (Single Enantiomer)

(182) MS (ESI) m/z: 223 (M+H).sup.+.

Amine-16: N-(4-(1-aminoethyl)-6-methylpyrimidin-2-yl)acetamide hydrochloride (Single Enantiomer)

(183) MS (ESI) m/z: 195 (M+H).sup.+.

Amine-17: N-(4-(1-aminoethyl)-6-methylpyrimidin-2-yl)propionamide hydrochloride (Single Enantiomer)

(184) MS (ESI) m/z: 209 (M+H).sup.+.

Amine-18: N-(4-(1-aminoethyl)-6-methylpyrimidin-2-yl)cyclopropanecarboxamide hydrochloride (Single Enantiomer)

(185) MS (ESI) m/z: 221 (M+H).sup.+.

Amine-19: N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)cyclopropanecarboxamide hydrochloride (Single Enantiomer)

(186) MS (ESI) m/z: 220 (M+H).sup.+.

Amine-20: N-(4-(1-aminoethyl)pyridin-2-yl)-3-methylbutanamide hydrochloride (Single Enantiomer)

(187) MS (ESI) m/z: 222 (M+H).sup.+.

Amine-21: N-(4-(1-aminoethyl)pyrimidin-2-yl)isobutyramide hydrochloride (Single Enantiomer)

(188) MS (ESI) m/z: 209 (M+H).sup.+.

Amine-22: N-(4-(1-aminoethyl)pyridin-2-yl)cyclobutanecarboxamide hydrochloride (Single Enantiomer)

(189) MS (ESI) m/z: 220 (M+H).sup.+.

Amine-23: N-(4-(1-aminoethyl)pyridin-2-yl)acrylamide hydrochloride (Single Enantiomer)

(190) MS (ESI) m/z: 192 (M+H).sup.+.

Amine-24: N-(4-(1-aminoethyl)pyridin-2-yl)butyramide hydrochloride (Single Enantiomer)

(191) MS (ESI) m/z: 208 (M+H).sup.+.

Amine-25: N-(4-(1-aminoethyl)pyridin-2-yl)cyclohexanecarboxamide hydrochloride (Single Enantiomer)

(192) MS (ESI) m/z: 248 (M+H).sup.+.

Amine-26: N-(4-(1-aminoethyl)pyridin-2-yl)pivalamide hydrochloride (Single Enantiomer)

(193) MS (ESI) m/z: 222 (M+H).sup.+.

Amine-27: N-(4-(1-aminoethyl)-6-methoxypyridin-2-yl)cyclopropanecarboxamide hydrochloride (Single Enantiomer)

(194) MS (ESI) m/z: 236 (M+H).sup.+.

Amine-28: N-(4-(1-aminoethyl)-6-methoxypyridin-2-yl)isobutyramide hydrochloride (Single Enantiomer)

(195) MS (ESI) m/z: 238 (M+H).sup.+.

Amine-29: N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)-2-hydroxy-2-methylpropanamide hydrochloride (Single Enantiomer)

(196) MS (ESI) m/z: 238 (M+H).sup.+.

(197) <Carboxylic Acid Part>

Carboxylic Acid-1: 5-methyl-6-(2,2,2-trifluoroethoxy)nicotinic acid

(198) To a suspension of sodium hydride (60% in mineral oil, 1.16 g, 29.0 mmol) in DMA (48 mL) is added 2,2,2-trifluoroethanol (1.39 mL, 19.3 mmol) at rt. After stirring at rt for 20 min, 6-fluoro-5-methylnicotinic acid (1.50 g, 9.67 mmol) is added to the suspension, and the mixture is stirred at 90 C. for 18 hours. After cooling to rt, the mixture is poured into 2 M hydrochloric acid (200 mL), and the aqueous layer is extracted with EtOAc-hexane (2:1, 300 mL). The combined organic layer is dried over sodium sulfate and concentrated in vacuo to give 2.27 g of the title compound as a yellow oil. This is used for the next step without further purification.

(199) MS (ESI) m/z: 234 (MH).sup.

(200) Carboxylic acid-2 to 8 are prepared according to the procedure similar to that described in Carboxylic acid-1, using the appropriate starting materials and reagents.

Carboxylic Acid-2: 4-methyl-6-(2,2,2-trifluoroethoxy)nicotinic acid

(201) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.06 (1H, br s), 8.63 (1H, s), 6.95 (1H, s), 5.04 (2H, q, J=9.2 Hz), 2.53 (3H, s), MS (ESI) m/z: 236 (M+H).sup.+.

Carboxylic Acid-3: 6-(2,2-difluoroethoxy)-5-methylnicotinic acid

(202) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.09 (1H, br s), 8.56 (1H, d, J=2.2 Hz), 8.07 (1H, d, J=2.2 Hz), 6.42 (1H, tt, J=54.3, 3.7 Hz), 4.66 (2H, td, J=14.7, 3.7 Hz), 2.21 (3H, s), MS (ESI) m/z: 218 (M+H).sup.+.

Carboxylic Acid-4: 5-methyl-6-(2,2,3,3-tetrafluoropropoxy)nicotinic acid

(203) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.74 (1H, d, J=2.2 Hz), 8.09 (1H, d, J=2.2 Hz), 6.00 (1H, tt, J=52.7, 3.7 Hz), 4.84 (2H, t, J=12.5 Hz), 2.28 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 268 (M+H)+, 266 (MH).sup..

Carboxylic Acid-5: 5-methyl-6-(3,3,3-trifluoropropoxy)nicotinic acid

(204) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.73 (1H, d, J=2.2 Hz), 8.04 (1H, d, J=2.2 Hz), 4.66 (2H, t, J=6.6 Hz), 2.75-2.55 (2H, m), 2.24 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 248 (MH).sup..

Carboxylic Acid-6: 6-(2,2-difluoropropoxy)nicotinic acid

(205) MS (ESI) m/z: 216 (MH).sup..

Carboxylic Acid-7: 5-chloro-6-(3,3,3-trifluoropropoxy)nicotinic acid

(206) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.77 (1H, d, J=2.2 Hz), 8.29 (1H, d, J=1.5 Hz), 4.72 (2H, t, J=6.6 Hz), 2.78-2.63 (2H, m) (a signal due to COOH is not observed),

(207) MS (ESI) m/z: 270 (M+H).sup.+.

Carboxylic Acid-8: 5-chloro-6-(2,2-difluoropropoxy)nicotinic acid

(208) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.77 (1H, d, J=2.2 Hz), 8.31 (1H, d, J=2.2 Hz), 4.64 (2H, t, J=11.7 Hz), 1.80 (3H, t, J=18.3 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 252 (M+H).sup.+.

Carboxylic Acid-9: 2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinic acid

: 2,2,2-trifluoroethyl 2-chloro-6-(2,2,2-trifluoroethoxyl)nicotinate

(209) To a mixture of 2-chloro-6-hydroxynicotinic acid (5.00 g, 23.1 mmol) and cesium carbonate (18.8 g, 57.6 mmol) in DMA (100 mL) is added dropwise 2,2,2-trifluoroethyl trifluoromethanesulfonate (6.65 mL, 46.1 mmol) at 0 C. After stirring at 0 C. for 4 h, the mixture is poured into water (300 mL), and the aqueous layer is extracted with EtOAc-toluene (2:1, 150 mL3). The combined organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (5:1) to give 4.81 g (63% yield) of the title compound as a white solid.

(210) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.26 (1H, d, J=8.4 Hz), 6.89 (1H, d, J=8.4 Hz), 4.81 (2H, q, J=8.4 Hz), 4.69 (2H, q, J=8.4 Hz).

: methyl 2-methoxy-6-(2,2,2-trifluoroethoxyl)nicotinate

(211) To a stirred solution of 2,2,2-trifluoroethyl 2-chloro-6-(2,2,2-trifluoroethoxyl)nicotinate (2.5 g, 7.41 mmol, Step-1) in THF (37 mL) is added sodium methoxide (1.20 g, 22.2 mmol) at rt. After stirring at rt for 2 h, the mixture is poured into saturated aqueous ammonium chloride solution (100 mL), and the aqueous layer is extracted with EtOAc (150 mL3). The combined organic layer is washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 1.90 g (97%) of the title compound. This is used for the next step without further purification.

(212) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.21 (1H, d, J=8.0 Hz), 6.47 (1H, d, J=8.0 Hz), 4.79 (2H, q, J=8.8 Hz), 4.07 (3H, s), 3.87 (3H, s), MS (ESI) m/z: 266 (M+H).sup.+.

: 2-methoxy-6-(2,2,2-trifluoroethoxy)nicotinic acid

(213) A mixture of methyl 2-methoxy-6-(2,2,2-trifluoroethoxyl)nicotinate (600 mg, 2.26 mmol, Step-2) and 2 M aqueous sodium hydroxide solution (2 mL) in THF (10 mL) is stirred at 60 C. for 12 hours. After cooling to rt, the mixture is neutralized by 2 M hydrochloric acid. This is poured into water (30 mL), and the aqueous layer is extracted with EtOAc (30 mL3). The combined organic layer is dried over sodium sulfate and concentrated in vacuo to give 535 mg (94%) of the tile compound as a white solid.

(214) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.41 (1H, d, J=8.8 Hz), 6.62 (1H, d, J=8.8 Hz), 4.81 (2H, q, J=8.0 Hz), 4.17 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 252 (M+H).sup.+.

(215) Carboxylic acid-10 to 18 are prepared according to the procedure similar to that described in Carboxylic acid-9, using the appropriate starting materials and reagents.

Carboxylic Acid-10: 2-methoxy-6-(3,3,3-trifluoropropoxy)nicotinic acid

(216) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 7.92 (1H, d, J=8.1 Hz), 6.30 (1H, d, J=8.1 Hz), 4.51 (2H, t, J=5.9 Hz), 3.84 (3H, s), 2.86-2.74 (2H, m) (a signal due to COOH is not observed), MS (ESI) m/z: 264 (MH).sup..

Carboxylic Acid-11: 6-(2,2-difluoroethoxy)-2-methoxynicotinic acid

(217) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.39 (1H, d, J=8.8 Hz), 6.59 (1H, d, J=8.0 Hz), 6.12 (1H, tt, J=54.9, 3.7 Hz), 4.60 (2H, td, J=13.2, 4.4 Hz), 4.17 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 234 (M+H).sup.+.

Carboxylic Acid-12: 2,6-bis(2,2,2-trifluoroethoxy)nicotinic acid

(218) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.38 (1H, d, J=8.1 Hz), 6.64 (1H, d, J=8.1 Hz), 6.44 (1H, br s), 4.90-4.65 (4H, m), MS (ESI) m/z: 320 (M+H).sup.+.

Carboxylic Acid-13: 2-(2-methoxyethoxy)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(219) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.42 (1H, d, J=8.8 Hz), 6.65 (1H, d, J=8.1 Hz), 4.77 (2H, q, J=8.8 Hz), 4.68-4.65 (2H, m), 3.86-3.78 (2H, m), 3.45 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 296 (M+H).sup.+.

Carboxylic Acid-14: 2-(2,2-difluoroethoxy)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(220) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.42 (1H, d, J=8.8 Hz), 6.67 (1H, d, J=8.8 Hz), 6.18 (1H, tt, J=55.0, 4.4 Hz), 4.81-4.70 (4H, m) (a signal due to COOH is not observed), MS (ESI) m/z: 302 (M+H).sup.+.

Carboxylic Acid-15: 2-(4-fluorophenoxy)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(221) .sup.1H-NMR (270 MHz, CDCl.sub.3) delta 8.45 (1H, d, J=8.6 Hz), 7.13 (4H, d, J=6.6 Hz), 6.66 (1H, d, J=8.6 Hz), 4.36 (2H, q, J=8.6 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 332 (M+H).sup.+.

Carboxylic Acid-16: 2-(3-methoxypropoxy)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(222) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 12.61 (1H, br s), 8.14 (1H, d, J=8.4 Hz), 6.56 (1H, d, J=8.4 Hz), 5.05 (2H, q, J=9.2 Hz), 4.40 (2H, t, J=6.2 Hz), 3.47 (2H, t, J=6.2 Hz), 3.22 (3H, s), 1.94 (2H, quintet, J=6.2 Hz), MS (ESI) m/z: 310 (M+H).sup.+.

Carboxylic Acid-17: 2-(2-(2-oxopyrrolidin-1-yl)ethoxy)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(223) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.09 (1H, d, J=8.2 Hz), 6.53 (1H, d, J=8.2 Hz), 5.04 (2H, q, J=8.8 Hz), 4.42 (2H, t, J=5.5 Hz), 3.56-3.22 (4H, m), 2.18 (2H, t, J=8.0 Hz), 1.93-1.81 (2H, m) (a signal due to COOH is not observed), MS (ESI) m/z: 349 (M+H).sup.+.

Carboxylic Acid-18: 2-(2-morpholinoethoxy)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(224) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.20 (1H, d, J=8.0 Hz), 6.66 (1H, d, J=8.0 Hz), 5.09 (2H, q, J=8.8 Hz), 4.85-4.72 (2H, m), 3.95-3.75 (4H, m), 3.56-3.05 (6H, m) (a signal due to COOH is not observed), MS (ESI) m/z: 351 (M+H).sup.+.

Carboxylic Acid-19: 5-fluoro-6-(2,2,2-trifluoroethoxy)nicotinic acid

: 2-chloro-5-fluoro-6-(2,2,2-trifluoroethoxy)nicotinic acid

(225) A mixture of 2,6-dichloro-5-fluoronicotinic acid (25.0 g, 119 mmol), 2,2,2-trifluoroethanol (17.1 mL, 238 mmol) and sodium hydroxide (14.3 g, 1.36 mol) in water (600 ml) is stirred for 40 hours at 80 C. After cooling to 0 C., the mixture is acidified by the addition of 2 M hydrochloric acid to give a white suspension, which is collected by filtration to give 32.2 g (99% yield) of the title compound as a white solid. This is used for the next step without further purification.

(226) MS (ESI) m/z: 274 (M+H).sup.+.

: 5-fluoro-6-(2,2,2-trifluoroethoxy)nicotinic acid

(227) A mixture of 2-chloro-5-fluoro-6-(2,2,2-trifluoroethoxy)nicotinic acid (32.2 g, 118 mmol, Step-1), triethylamine (23.0 mL, 165 mmol), and 10% palladium on activated carbon (1.0 g) in ethanol (600 mL) is stirred at rt for 5 hours under a hydrogen atmosphere (1 atm). The mixture is filtered through a pad of Celite, and the filtrate is concentrated in vacuo. The residue is dissolved in water (300 mL) and acidified by 2 M hydrochloric acid. The formed precipitate is collected by filtration to give 21.0 g (75%) of the title compound as a white solid.

(228) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.40 (1H, br), 8.55 (1H, d, J=1.8 Hz), 8.13 (1H, dd, J=10.3, 1.8 Hz), 5.16 (2H, q, J=9.2 Hz), MS (ESI) m/z: 238 (MH).sup..

Carboxylic Acid-20: 6-(3,3,3-trifluoropropyl)nicotinic acid

: (3,3,3-trifluoropropyl)magnesium bromide

(229) Magnesium (0.30 g, 12.4 mmol) is added to flame dried flask. To the flask is added a solution of 3-bromo-1,1,1-trifluoropropane (1.2 mL, 11.3 mmol) in THF (11 mL), and the mixture is refluxed with stirring for 2 hours. This material is used for the next step.

: methyl 6-(3,3,3-trifluoropropyl)nicotinate

(230) To a solution of methyl 6-chloronicotinate (0.70 g, 4.08 mmol), iron(III) acetylacetonate (0.14 g, 0.41 mmol) and 1-methyl-2-pyrrolidinone (0.23 mL, 2.39 mmol) in THF (23 mL) is added (3,3,3-trifluoropropyl)magnesium bromide (8.16 mL, 8.16 mmol, Step-1), and the mixture is stirred at rt for 30 minutes. The reaction mixture is poured into water, and the aqueous layer is extracted with EtOAc. The separated organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (3:1) to give 0.95 g (99% yield) of the title compound as a white solid.

(231) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 9.14 (1H, d, J=2.2 Hz), 8.22 (1H, dd, J=8.1, 2.2 Hz), 7.27 (1H, d, J=8.1 Hz), 3.95 (3H, s), 3.13-3.08 (2H, m), 2.71-2.55 (2H, m), MS (ESI) m/z: 234 (M+H).sup.+.

: 6-(3,3,3-trifluoropropyl)nicotinic acid

(232) The title compound is prepared in quantitative yield (987 mg, a white solid) from methyl 6-(3,3,3-trifluoropropyl)nicotinate (949 mg, Step-2) in a similar manner to Step-3 of Carboxylic acid-9.

(233) MS (ESI) m/z: 220 (M+H).sup.+.

(234) Carboxylic acid-21 is prepared according to the procedure similar to that described in Carboxylic acid-20, using the appropriate starting materials and reagents.

Carboxylic Acid-21: 5-methyl-6-(3,3,3-trifluoropropyl)nicotinic acid

(235) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.82 (1H, s), 8.04 (1H, s), 3.05-3.00 (2H, m), 2.83-2.70 (2H, m), 2.34 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 232 (MH).sup..

Carboxylic Acid-22: 4-(2,2-difluoroethoxy)-3-methylbenzoic acid

: methyl 4-(2,2-difluoroethoxy)-3-methylbenzoate

(236) To a solution of methyl 4-hydroxy-3-methylbenzoate (1.50 g, 9.03 mmol), 2,2-difluoroethanol (889 mg, 10.8 mmol), and triphenylphosphine (3.55 g, 13.5 mmol) in THF (40 mL) is added dropwise diethyl azodicarboxylate (40% in toluene solution, 4.92 mL, 10.8 mmol) at 0 C. The mixture is stirred at rt for 30 min, then at 60 C. for 2 hours. After removal of solvent, the residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (18:1) to give 1.86 g (90% yield) of the title compound as a white crystalline.

(237) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.90-7.85 (2H, m), 6.79 (1H, d, J=8.8 Hz), 6.13 (1H, tt, J=54.9, 4.4 Hz), 4.24 (2H, dt, J=12.5, 3.7 Hz), 3.89 (3H, s), 2.27 (3H, s).

: 4-(2,2-difluoroethoxy)-3-methylbenzoic acid

(238) The title compound is prepared in quantitative yield (1.06 g, a white solid) from methyl 4-(2,2-difluoroethoxy)-3-methylbenzoate (1.0 g, Step-1) in a similar manner to Step-3 of Carboxylic acid-9.

(239) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.97-7.90 (2H, m), 6.83 (1H, d, J=8.1 Hz), 6.14 (1H, tt, J=54.9, 4.4 Hz), 4.26 (2H, dt, J=12.5, 4.4 Hz), 2.28 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 215 (MH).sup..

(240) Carboxylic acid-23 to 26 are prepared according to the procedure similar to that described in Carboxylic acid-22, using the appropriate starting materials and reagents.

Carboxylic Acid-23: 5-(3,3,3-trifluoropropoxy)picolinic acid

(241) MS (ESI) m/z: 234 (MH).sup..

Carboxylic Acid-24: 3-(3,3,3-trifluoropropoxyl)benzoic acid

(242) MS (ESI) m/z: 233 (MH).sup..

Carboxylic Acid-25: 3-methoxy-4-(2,2,2-trifluoroethoxyl)benzoic acid

(243) MS (ESI) m/z: 249 (MH).sup..

Carboxylic Acid-26: 2-methoxy-4-(2,2,2-trifluoroethoxyl)benzoic acid

(244) .sup.1H-NMR (270 MHz, CDCl.sub.3) delta 8.19 (1H, d, J=8.2 Hz), 6.66-6.62 (2H, m), 4.43 (2H, q, J=7.9 Hz), 4.07 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 251 (M+H).sup.+.

Carboxylic Acid-27: 6-(2,2,3,3,3-pentafluoropropoxy)nicotinic acid

: methyl 6-(2,2,3,3,3-pentafluoropropoxy)nicotinate

(245) To a stirred suspension of sodium hydride (4.9 g, 120 mmol, 60% in oil) in DMA (100 mL) is added dropwise 2,2,3,3,3-pentafluoropropan-1-ol (8.1 mL, 82 mmol) at 0 C. After stirring for 10 minutes, a solution of methyl 6-chloronicotinate (7.0 g, 41 mmol) in DMA (120 mL) is added dropwise to the suspension at 0 C., and the mixture is stirred for 30 minutes at rt. Then, the mixture is stirred at 90 C. for 2 hours. After cooled to rt, 2M aqueous sodium hydroxide is added (pH is around 6). The mixture is extracted with hexane/EtOAc (1:2, 200 mL). The organic layer is washed with water, brine, and dried over sodium sulfate. The organic solvent is concentrated under reduced pressure to give 8.4 g of the title compound as a crude product (include 2,2,3,3,3-pentafluoropropyl 6-(2,2,3,3,3-pentafluoropropoxy)nicotinate as a byproduct). The residue is used for the next step without further purification.

(246) MS (ESI) m/z: 286 (M+H).sup.+.

:6-(2,2,3,3,3-pentafluoropropoxy)nicotinic acid

(247) The title compound is prepared in 62% yield (6.8 g, an off-white solid, yield is based on methyl 6-chloronicotinate) from methyl 6-(2,2,3,3,3-pentafluoropropoxy)nicotinate (8.4 g, crude from Step-1) in a similar manner to Step-3 of Carboxylic acid-9.

(248) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.90 (1H, d, J=2.2 Hz), 8.29 (1H, dd, J=8.8, 2.2 Hz), 6.94 (1H, d, J=8.8 Hz), 4.93 (2H, t, J=11.7 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 270 (MH).sup..

(249) Carboxylic acid-28 is prepared according to the procedure similar to that described in Carboxylic acid-27, using the appropriate starting materials and reagents.

Carboxylic Acid-28: 1-(2,2,2-trifluoroethoxyl)isoquinoline-4-carboxylic acid

(250) MS (ESI) m/z: 272 (M+H).sup.+.

Carboxylic Acid-29: 2-fluoro-4-(2,2,2-trifluoroethoxy)benzoic acid

: 2,2,2-trifluoroethyl 2-fluoro-4-(2,2,2-trifluoroethoxy)benzoate

(251) To a mixture of 2-fluoro-4-hydroxybenzoic acid (500 mg, 3.20 mmol) and potassium carbonate (2.21 g, 16.0 mmol) in DMF (8 mL) is added 2,2,2-trifluoroethyl trifluoromethanesulfonate (2.23 g, 9.61 mmol), and the mixture is stirred at 80 C. for 2 hours. After cooling to rt, the mixture is poured into water (100 mL), and the aqueous layer is extracted with EtOAc (100 mL2). The combined organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (10:1) to give 792 mg (77% yield) of the title compound as a colorless oil.

(252) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.99 (1H, t, J=8.8 Hz), 6.81 (1H, dd, J=8.8, 2.9 Hz), 6.73 (1H, dd, J=11.7, 2.9 Hz), 4.69 (2H, q, J=8.1 Hz), 4.41 (2H, q, J=8.1 Hz).

: 2-fluoro-4-(2,2,2-trifluoroethoxyl)benzoic acid

(253) The title compound is prepared in 89% yield (525 mg, a white solid) from 2,2,2-trifluoroethyl 2-fluoro-4-(2,2,2-trifluoroethoxyl)benzoate (790 mg, Step-1) in a similar manner to Step-3 of Carboxylic acid-9.

(254) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 7.87 (1H, t, J=8.8 Hz), 7.09 (1H, dd, J=13.2, 2.9 Hz), 6.99 (1H, dd, J=8.8 Hz), 4.89 (2H, q, J=8.8 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 237 (MH).sup..

(255) Carboxylic acid-30 to 32 is prepared according to the procedure similar to that described in Carboxylic acid-29, using the appropriate starting materials and reagents.

Carboxylic Acid-30: 3-methyl-4-(2,2,2-trifluoroethoxyl)benzoic acid

(256) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.98-7.90 (2H, m), 6.83 (1H, d, J=8.0 Hz), 4.43 (2H, q, J=7.3 Hz), 2.31 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 233 (MH).sup..

Carboxylic Acid-31: 4-(2,2-difluoropropoxy)-3-methylbenzoic acid

(257) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 12.67 (1H, br s), 7.80-7.76 (2H, m), 7.08 (1H, d, J=8.1 Hz), 4.37 (2H, t, J=12.5 Hz), 2.21 (3H, s), 1.77 (3H, t, J=19.1 Hz), MS (ESI) m/z: 231 (M+H).sup.+.

Carboxylic Acid-32: 3-chloro-4-(2,2-difluoropropoxy)benzoic acid

(258) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 7.92 (1H, d, J=1.8 Hz), 7.88 (1H, dd, J=8.4, 1.8 Hz), 7.32 (1H, d, J=8.4 Hz), 4.48 (2H, t, J=12.4 Hz), 1.76 (3H, t, J=19.4 Hz),

(259) MS (ESI) m/z: 249 (MH).sup..

Carboxylic Acid-33: 6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylic acid

: methyl 6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate

(260) To a suspension of sodium hydride (60% in mineral oil, 232 mg, 5.79 mmol) in DMF is added 2,2,2-trifluoroethanol (580 mg, 5.79 mmol) at 0 C., and the mixture is stirred at rt for 15 min. Then, methyl 6-chloropyridazine-3-carboxylate (500 mg, 2.90 mmol) is added, and the mixture is stirred at rt for 1 hour. Then, the mixture is poured into water (100 mL), and the aqueous layer is extracted with EtOAc (100 mL2). The combined organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (3:1 to 1:1) to give 159 mg (23% yield) of the title compound as a white solid.

(261) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.17 (1H, d, J=8.8 Hz), 7.23 (1H, d, J=8.8 Hz), 5.03 (2H, q, J=8.0 Hz), 4.06 (3H, s), MS (ESI) m/z: 237 (M+H).sup.+.

: 6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylic acid

(262) The title compound is prepared in 99% yield (145 mg, a white solid) from methyl 6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate (155 mg, Step-1) in a similar manner to Step-3 of Carboxylic acid-9.

(263) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.18 (1H, d, J=8.8 Hz), 7.55 (1H, d, J=8.1 Hz), 5.28 (2H, q, J=8.8 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 221 (MH).sup..

(264) Carboxylic acid-34 and 35 is prepared according to the procedure similar to that described in Carboxylic acid-33, using the appropriate starting materials and reagents.

Carboxylic Acid-34: 6-(2,2,3,3,3-pentafluoropropoxy)pyridazine-3-carboxylic acid

(265) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.8 (1H, brs), 8.19 (1H, d, J=9.51 Hz), 7.55 (1H, d, J=9.51 Hz), 5.39 (2H, t, J=12.4 Hz), MS (ESI) m/z: 273 (M+H).sup.+.

Carboxylic Acid-35: 6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxylic acid

(266) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.15 (1H, d, J=8.8 Hz), 7.45 (1H, d, J=8.8 Hz), 6.74 (1H, dt, J=51.2, 5.9 Hz), 5.14 (2H, t, J=13.9 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 253 (MH).sup..

Carboxylic Acid-36: 1-methyl-5-(2,2,2-trifluoroethoxy)-1H-pyrazole-3-carboxylic acid

: methyl 1-methyl-5-(2,2,2-trifluoroethoxy)-1H-pyrazole-3-carboxylate

(267) The title compound is prepared in 95% yield (290 mg, a white solid) from methyl 5-hydroxy-1-methyl-1H-pyrazole-3-carboxylate (200 mg, 1.28 mmol) in a similar manner to Step-1 of Carboxylic acid-29.

(268) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 6.16 (1H, s), 4.43 (2H, q, J=7.3 Hz), 3.92 (3H, s), 3.78 (3H, s), MS (ESI) m/z: 239 (M+H).sup.+.

: 1-methyl-5-(2,2,2-trifluoroethoxy)-1H-pyrazole-3-carboxylic acid

(269) The title compound is prepared in quantitative yield (290 mg, a white solid) from methyl 1-methyl-5-(2,2,2-trifluoroethoxy)-1H-pyrazole-3-carboxylate (290 mg, 1.22 mmol) in a similar manner to Step-3 of Carboxylic acid-9.

(270) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 6.33 (1H, s), 4.94 (2H, q, J=8.8 Hz), 3.65 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 223 (MH).sup..

(271) Carboxylic acid-37 is prepared according to the procedure similar to that described in carboxylic acid-36, using the appropriate starting materials and reagents.

Carboxylic Acid-37: 1-methyl-5-(2,2,3,3,3-pentafluoropropoxy)-1H-pyrazole-3-carboxylic acid

(272) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 12.7 (1H, brs), 6.39 (1H, s), 5.05 (2H, t, J=13.2 Hz), 3.64 (3H, s), MS (ESI) m/z: 273 (MH).sup..

Carboxylic Acid-38: 6-methyl-5-(2,2,2-trifluoroethoxy)picolinic acid

: 6-iodo-2-methyl-3-(2,2,2-trifluoroethoxyl)pyridine

(273) The title compound is prepared in quantitative yield (2.96 g, a colorless oil) from 6-iodo-2-methylpyridin-3-ol (2.10 g, 8.91 mmol) in a similar manner to Step-1 of Carboxylic acid-29.

(274) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.57 (1H, d, J=8.79 Hz), 6.79 (1H, d, J=8.04 Hz), 4.33 (2H, q, J=8.07 Hz), 2.49 (3H, s), MS (ESI) m/z: 317 (M+H).sup.+.

: ethyl 6-methyl-5-(2,2,2-trifluoroethoxy)picolinate

(275) A mixture of 6-iodo-2-methyl-3-(2,2,2-trifluoroethoxyl)pyridine (2.95 g, 9.30 mmol, Step-1), palladium(II) acetate (209 mg, 0.93 mmol), 1,1-bis(diphenylphosphino)ferrocene (1.03 g, 1.86 mmol), and triethylamine (2.59 mL, 18.6 mmol) in ethanol-DMF (1:1, 40 mL) is stirred at 60 C. for 12 hours under carbon monoxide atmosphere. After cooling to rt, the mixture is filtered through a pad of Celite, and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (10:1) to give 2.29 g (93% yield) of the title compound as a brown solid.

(276) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.01 (1H, d, J=8.8 Hz), 7.13 (1H, d, J=8.0 Hz), 4.46 (2H, q, J=7.3 Hz), 4.44 (2H, q, J=7.3 Hz), 2.60 (3H, s), 1.43 (3H, t, J=7.3 Hz),

(277) MS (ESI) m/z: 264 (M+H).sup.+.

: 6-methyl-5-(2,2,2-trifluoroethoxy)picolinic acid

(278) The title compound is prepared in 91% yield (1.86 g, a white solid) from ethyl 6-methyl-5-(2,2,2-trifluoroethoxy)picolinate (2.29 g, 8.70 mmol, Step-2) in a similar manner to Step-3 of Carboxylic acid-9.

(279) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 7.93 (1H, d, J=8.1 Hz), 7.56 (1H, d, J=8.8 Hz), 4.92 (2H, q, J=8.8 Hz), 2.42 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 234 (MH).sup..

Carboxylic Acid-39: 6-methyl-2-(2,2,2-trifluoroethoxy)nicotinic acid

: 6-chloro-2-(2,2,2-trifluoroethoxy)nicotinic acid

(280) A mixture of 2,6-dichloronicotinic acid (3.00 g, 15.6 mmol), potassium tert-butoxide (5.26 g, 46.9 mmol), and 2,2,2-trifluoroethanol (52 mL) is refluxed with stirring for 5 days. After cooling to rt, excess 2,2,2-trifluoroethanol is evaporated in vacuo. The residue is poured into water, and the mixture is acidified by 2 M hydrochloric acid. The formed precipitate is collected by filtration to give 4.08 g of the title compound, which contains 2-chloro-6-(2,2,2-trifluoroethoxy)nicotinic acid. This is used for the next step without further purification.

(281) MS (ESI) m/z: 256 (M+H).sup.+.

: methyl 6-chloro-2-(2,2,2-trifluoroethoxyl)nicotinate

(282) To a solution of 6-chloro-2-(2,2,2-trifluoroethoxy)nicotinic acid (4.08 g, Step-1) in MeOH (50 mL) is added thionyl chloride (4.66 mL, 63.9 mmol) at 0 C. The mixture is refluxed with stirring for 2.5 hours. After cooling to rt, the solvent is evaporated in vacuo. The residual oil is purified by column chromatography on silica gel eluting with hexane/EtOAc (20:1) to give 2.90 g of the title compound, which contains methyl 2-chloro-6-(2,2,2-trifluoroethoxyl)nicotinate. This is used for the next step without further purification.

(283) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.22 (1H, d, J=8.0 Hz), 7.09 (1H, d, J=8.0 Hz), 4.83 (2H, q, J=8.4 Hz), 3.92 (3H, s), MS (ESI) m/z: 270 (M+H).sup.+.

: methyl 6-methyl-2-(2,2,2-trifluoroethoxyl)nicotinate

(284) To a solution of methyl 6-chloro-2-(2,2,2-trifluoroethoxyl)nicotinate (2.70 g, Step-2) and [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II) dichloromethane complex (816 mg, 1.0 mmol) in dioxane (50 mL) is added dropwise a solution of dimethylzinc (1.0 M hexane solution, 40.0 mL) at rt. The mixture is stirred at 75 C. for 1 hour. After cooling to rt, the reaction is carefully quenched by water. The mixture is diluted with EtOAc and water, and filtered through a pad of Celite. The filtrate is extracted with EtOAc. The combined organic layer is washed with water, dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (20:1) to give 1.51 g (39% from 2,6-dichloronicotinic acid) of the title compound as a white solid.

(285) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.13 (1H, d, J=7.7 Hz), 6.89 (1H, d, J=7.7 Hz), 4.85 (2H, q, J=8.6 Hz), 3.89 (3H, s), 2.48 (3H, s), MS (ESI) m/z: 250 (M+H).sup.+.

: 6-methyl-2-(2,2,2-trifluoroethoxy)nicotinic acid

(286) The title compound is prepared in quantitative yield (94 mg, a white solid) from methyl 6-methyl-2-(2,2,2-trifluoroethoxyl)nicotinate (100 mg, 0.40 mmol, Step-3) in a similar manner to Step-3 of Carboxylic acid-9.

(287) MS (ESI) m/z: 236 (M+H).sup.+.

Carboxylic Acid-40: 2-morpholino-6-(2,2,2-trifluoroethoxy)nicotinic acid

: 2,2,2-trifluoroethyl 2-morpholino-6-(2,2,2-trifluoroethoxyl)nicotinate

(288) A mixture of 2,2,2-trifluoroethyl 2-chloro-6-(2,2,2-trifluoroethoxyl)nicotinate (0.30 g, 0.89 mmol, Step-1 of Carboxylic acid-9), morpholine (0.77 mL, 8.89 mmol) and triethylamine (0.62 mL, 4.44 mmol) in THF (2 mL) is stirred at 140 C. for 10 min under microwave irradiation. The reaction mixture is poured into water, and the aqueous layer is extracted with EtOAc. The organic layer is dried over sodium sulfate and concentrated in vacuo to give 0.35 g (>99% yield) of the title compound as a yellow solid. This material is used for the next step without further purification.

(289) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.16 (1H, d, J=8.4 Hz), 6.33 (1H, d, J=8.4 Hz), 4.72 (2H, q, J=8.4 Hz), 4.63 (2H, q, J=8.4 Hz), 3.82 (4H, t, J=4.8 Hz), 3.44 (4H, t, J=4.8 Hz), MS (ESI) m/z: 389 (M+H).sup.+.

: 2-morpholino-6-(2,2,2-trifluoroethoxy)nicotinic acid

(290) The title compound is prepared in quantitative yield from 2,2,2-trifluoroethyl 2-morpholino-6-(2,2,2-trifluoroethoxyl)nicotinate (230 mg, Step-1) in a similar manner to Step-3 of Carboxylic acid-9.

(291) MS (ESI) m/z: 307 (M+H).sup.+.

(292) Carboxylic acid-41 to 45 are prepared according to the procedure similar to that described in Carboxylic acid-40, using the appropriate starting materials and reagents.

Carboxylic Acid-41: 2-(piperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(293) MS (ESI) m/z: 305 (M+H).sup.+.

Carboxylic Acid-42: 2-(4-methoxypiperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(294) MS (ESI) m/z: 335 (M+H).sup.+.

Carboxylic Acid-43: 2-((2-methoxyethyl)(methyl)amino)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(295) MS (ESI) m/z: 309 (M+H).sup.+.

Carboxylic Acid-44: 2-(4-methylpiperazin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(296) MS (ESI) m/z: 320 (M+H).sup.+.

Carboxylic Acid-45: 2-(4-hydroxypiperidin-1-yl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(297) MS (ESI) m/z: 321 (M+H).sup.+.

Carboxylic Acid-46: 2-(4-fluorophenyl)-6-(2,2,2-trifluoroethoxy)nicotinic acid

(298) A mixture of 2,2,2-trifluoroethyl 2-chloro-6-(2,2,2-trifluoroethoxyl)nicotinate (200 mg, 0.59 mmol, Step-1 of Carboxylic acid-9), 4-fluorophenylboronic acid (166 mg, 1.19 mmol), tetrakis(triphenylphosphine)palladium(0) (137 mg, 0.12 mmol), and saturated aqueous sodium bicarbonate solution (3 mL) in DME (12 mL) is refluxed with stirring for 16 hours. After cooling to rt, the mixture is filtered through a pad of Celite. The filtrate is concentrated in vacuo. The residue is poured into water, the mixture is acidified by 2 M hydrochloric acid, and extracted with EtOAc. The separated organic layer is washed with water, dried over sodium sulfate, and concentrated in vacuo. The residual solid is washed with hexane to give 146 mg (78%) of the title compound as a white solid.

(299) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.09 (1H, br s), 8.15 (1H, d, J=8.4 Hz), 7.66-7.58 (2H, m), 7.31-7.23 (2H, m), 7.04 (1H, d, J=8.4 Hz), 5.08 (2H, q, J=8.8 Hz), MS (ESI) m/z: 316 (M+H).sup.+.

Carboxylic Acid-47: 5-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylic acid

: A mixture of 6-chloro-4-methyl-3-(2,2,2-trifluoroethoxyl)pyridazine and 3-chloro-4-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine (2:1)

(300) To a stirred solution of 2,2,2-trifluoroethanol (2.03 g, 20.2 mmol), DMF (20 mL) and THF (10 mL) is added 60% sodium hydride (0.78 g, 20.2 mmol) at 0 C. carefully. After stirring at rt for 1 hour, this solution is added to a solution of 3,6-dichloro-4-methylpyridazine (3.00 g, 18.4 mmol) in DMF (20 mL) at 0 C. slowly. The resulting mixture is stirred at rt for 1 hour. The mixture is poured into ice-water, and the aqueous layer is extracted with EtOAc (200 mL). The organic layer is washed with water (200 mL2), and dried over sodium sulfate. After removal of the organic solvent, the residue is purified by column chromatography on silica-gel eluting with n-hexane/EtOAc (9:1) to give 3.40 g of a mixture of the title compound (81% yield) as a white solid.

(301) MS (ESI) m/z: 227 (M+H).sup.+.

: ethyl 5-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate and ethyl 4-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate

(302) A mixture of 6-chloro-4-methyl-3-(2,2,2-trifluoroethoxyl)pyridazine and 3-chloro-4-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine (3.40 g, 15.0 mmol, Step-1), palladium(II) acetate (0.34 g, 1.50 mmol), 1,3-bis(diphenylphosphino)propane (1.24 g, 3.00 mmol), triethylamine (6.27 mL, 45.0 mmol), DMF (40 mL), and EtOH (20 mL) is stirred at 80 C. under carbon monoxide atmosphere (1 atm) for 20 hours. After cooling to rt, the mixture is diluted with EtOAc (200 mL). The organic layer is washed with water (200 mL2), and the organic layer is dried over sodium sulfate. After removal of the organic solvent, the residue is purified by column chromatography on silica-gel eluting with n-hexane/EtOAc (8:1-5:1) to give 2.15 g of ethyl 5-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate (54% yield, more polar product) as an off-white solid and 0.63 g of ethyl 4-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate (16% yield, less polar product) as pale yellow oil.

ethyl 5-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate (More Polar)

(303) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.99 (1H, d, J=1.5 Hz), 5.02 (2H, q, J=8.1 Hz), 4.50 (2H, q, J=7.3 Hz), 2.36 (3H, s), 1.46 (3H, t, J=7.3 Hz), MS (ESI) m/z: 265 (M+H).sup.+.

ethyl 4-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate (Less Polar)

(304) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.00 (1H, s), 4.99 (2H, q, J=8.1 Hz), 4.49 (2H, q, J=7.3 Hz), 2.58 (3H, s), 1.46 (3H, t, J=7.3 Hz), MS (ESI) m/z: 265 (M+H).sup.+.

:5-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylic acid

(305) The title compound is prepared in >99% yield (1.17 g, a pale brown solid) from ethyl 5-methyl-6-(2,2,2-trifluoroethoxyl)pyridazine-3-carboxylate (1.32 g, 5.00 mmol, Step-2) in a similar manner to Step-3 of Carboxylic acid-9.

(306) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.98 (1H, s), 5.19 (2H, q, J=8.8 Hz), 2.23 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 237 (M+H).sup.+.

(307) Carboxylic acid-48 is prepared according to the procedure similar to that described in carboxylic acid-47, using the appropriate starting materials and reagents.

Carboxylic Acid-48: 5-methyl-6-(2,2,3,3-tetrafluoropropoxy)pyridazine-3-carboxylic acid

(308) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.09 (1H, s), 6.76 (1H, tt, J=51.9, 5.1 Hz), 5.14 (2H, t, 13.2 Hz), 2.29 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 267 (MH).sup..

Carboxylic Acid-49: 4-methyl-5-(2,2,2-trifluoroethoxy)picolinic acid

:2-chloro-4-methyl-5-(2,2,2-trifluoroethoxyl)pyridine

(309) To a mixture of 6-chloro-4-methylpyridin-3-ol (2.00 g, 13.9 mmol) and cesium carbonate (6.81 g, 20.9 mmol) in DMF (40 mL) is added dropwise 2,2,2-trifluoroethyl trifluoromethanesulfonate (3.56 g, 15.3 mmol) at 0 C. After stirring at rt for 1 hour, the mixture is poured into water (300 mL). The aqueous layer is extracted with EtOAc (300 mL). The separated organic layer is washed with water (200 mL), dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with n-hexane/EtOAc (9:1) to give 3.00 g (95% yield) of the title compound as a white solid.

(310) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 7.90 (1H, s), 7.17 (1H, s), 4.43 (2H, q, J=7.3 Hz), 2.28 (3H, s), MS (ESI) m/z: 226 (M+H).sup.+.

: ethyl 4-methyl-5-(2,2,2-trifluoroethoxy)picolinate

(311) The title compound is prepared in 90% yield (3.14 g, a white solid) from 2-chloro-4-methyl-5-(2,2,2-trifluoroethoxyl)pyridine (3.00 g, 13.3 mmol, Step-1) in a similar manner to Step-2 of Carboxylic acid-47.

(312) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.24 (1H, s), 8.00 (1H, s), 4.57-4.42 (4H, m), 2.35 (3H, s), 1.44 (3H, t, J=6.6 Hz), MS (ESI) m/z: 264 (M+H).sup.+.

: 4-methyl-5-(2,2,2-trifluoroethoxy)picolinic acid

(313) The title compound is prepared in 92% yield (2.72 g, a white solid) from ethyl 4-methyl-5-(2,2,2-trifluoroethoxy)picolinate (3.30 g, 12.5 mmol, Step-2) in a similar manner to Step-3 of Carboxylic acid-9.

(314) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 8.12 (1H, s), 8.09 (1H, s), 4.55 (2H, q, J=7.6 Hz), 2.39 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 236 (M+H)+, 234 (MH).sup..

(315) Carboxylic acid-50 to 53 are prepared according to the procedure similar to that described in Carboxylic acid-49, using the appropriate starting materials and reagents.

Carboxylic Acid-50: 5-(2,2-difluoroethoxy)-4-methylpicolinic acid

(316) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.41 (1H, s), 7.93 (1H, s), 6.45 (1H, tt, J=54.2, 3.3 Hz), 4.58 (2H, td, J=14.7, 2.9 Hz), 2.25 (3H, s), MS (ESI) m/z: 218 (M+H).sup.+.

Carboxylic Acid-51: 4-methyl-5-(3,3,3-trifluoropropoxy)picolinic acid

(317) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.43 (1H, s), 8.04 (1H, s), 4.50 (2H, t, J=5.1 Hz), 3.0-2.8 (2H, m), 2.28 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 250 (M+H).sup.+.

Carboxylic acid-52

5-((4-fluorobenzyl)oxy)-4-methylpicolinic acid

(318) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.42 (1H, s), 7.92 (1H, s), 7.59-7.51 (2H, m), 7.28-7.21 (2H, m), 5.35 (2H, s), 2.26 (3H, s), MS (ESI) m/z: 262 (M+H).sup.+.

Carboxylic Acid-53: 5-(2,2-difluoropropoxy)-4-methylpicolinic acid

(319) .sup.1H-NMR (270 MHz, DMSO-d.sub.6) delta 8.40 (1H, s), 7.93 (1H, s), 4.56 (2H, t, J=12.5 Hz), 2.26 (3H, s), 1.78 (3H, t, J=19.1 Hz), MS (ESI) m/z: 232 (M+H).sup.+.

Carboxylic Acid-54: 6-methyl-5-(2,2,2-trifluoroethoxyl)pyrazine-2-carboxylic acid

: methyl 6-methyl-5-(2,2,2-trifluoroethoxyl)pyrazine-2-carboxylate

(320) A mixture of methyl 5-chloro-6-methylpyrazine-2-carboxylate (3.00 g, 16.1 mmol), 2,2,2-trifluoroethanol (32.2 g, 322 mmol), and potassium carbonate (3.33 g, 24.1 mmol) in DMF (30 mL) is stirred at 60 C. for 2 hours. After cooling to rt, the mixture is filtered off, and the filtrate is diluted with EtOAc (300 mL). The organic layer is washed with water (100 mL3) and dried over sodium sulfate. After filtration, the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting EtOAc to give 3.91 g (97% yield) of the title compound as a white solid.

(321) MS (ESI) m/z: 251 (M+H).sup.+.

: 6-methyl-5-(2,2,2-trifluoroethoxyl)pyrazine-2-carboxylic acid

(322) The title compound is prepared in 66% yield (2.44 g, a white solid) from methyl 6-methyl-5-(2,2,2-trifluoroethoxyl)pyrazine-2-carboxylate (3.91 g, 15.6 mmol, Step-1) in a similar manner to Step-3 of Carboxylic acid-9.

(323) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.36 (1H, br s), 8.67 (1H, s), 5.11 (2H, q, J=8.8 Hz), 2.48 (3H, s), MS (ESI) m/z: 235 (MH).sup..

Carboxylic Acid-55: 5-methyl-6-((2,2,2-trifluoroethyl)amino)nicotinic acid

(324) A mixture of methyl 6-fluoro-5-methylnicotinate (2.00 g, 11.8 mmol) and 2,2,2-trifluoroethanamine (9.37 g, 95 mmol) in N-methylpyrrolidone (24 mL) is stirred at 220 C. for 2.5 hours under microwave irradiation. The mixture is diluted with MeOH (30 mL), and 2 M aqueous sodium hydroxide solution (15 mL) is added to the mixture. After stirring at 50 C. for 1 hour, the mixture is acidified by 2 M hydrochloric acid, and extracted with EtOAc/hexane (100 mL3). The combined organic layer is washed with water (100 mL), and dried over sodium sulfate. After filtration, the filtrate is concentrated in vacuo. The residue is crystallized from diisopropyl ether to give 884 mg (32%) of the title compound as a pale pink solid.

(325) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.49 (1H, s), 7.78 (1H, s), 7.17 (1H, t, J=6.6 Hz), 4.35-4.21 (2H, m), 2.14 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 233 (MH).sup..

Carboxylic Acid-56: 5-methyl-6-(2-(2,2,2-trifluoroethoxy)ethoxy)nicotinic acid

(326) To a mixture of 2-(2,2,2-trifluoroethoxyl)ethanol (1.64 g, 11.4 mmol) and potassium tert-butoxide (1.38 g, 12.3 mmol) in DMF (30 mL) is added 6-fluoro-5-methylnicotinate (1.60 g, 9.46 mmol) at 0 C., and the mixture is stirred at rt for 1 hour. Then, MeOH (30 mL) and 0.7 M sodium hydroxide aqueous solution (45 mL) are added to the mixture. After stirring at rt for 1 hour, MeOH is evaporated in vacuo. The residual aqueous phase is acidified by 2 M hydrochloric acid, and the formed precipitate is collected by filtration to give 1.95 g (74%) of the title compound as a white solid.

(327) .sup.1H-NMR (300 MHz, DMSO-d.sub.3) delta 12.98 (1H, br s), 8.55 (1H, s), 8.01 (1H, s), 4.52-4.49 (2H, m), 4.16 (2H, q, J=9.5 Hz), 3.98-3.95 (2H, m), 2.19 (3H, s), MS (ESI) m/z: 280 (M+H).sup.+.

(328) Carboxylic acid-57 to 60 are prepared according to the procedure similar to that described in Carboxylic acid-56, using the appropriate starting materials and reagents.

Carboxylic Acid-57: 6-(2,2-difluoropropoxy)-5-methylnicotinic acid

(329) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.56 (1H, d, J=1.5 Hz), 8.07 (1H, d, J=1.5 Hz), 4.64 (2H, t, J=13.2 Hz), 2.22 (3H, s), 1.75 (3H, t, J=19.1 Hz) (a signal due to COOH is not observed), MS (ESI) m/z: 230 (MH).sup..

Carboxylic Acid-58: 6-((4-fluorobenzyl)oxy)-5-methylnicotinic acid

(330) .sup.1H-NMR (300 MHz, CDCl.sub.3/DMSO-d.sub.6) delta 8.69 (1H, d, J=2.2 Hz), 8.01 (1H, d, J=2.2 Hz), 7.45 (2H, dd, J=8.0, 5.1 Hz), 7.06 (2H, t, J=8.8 Hz), 5.43 (2H, s), 2.24 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 260 (MH).sup..

Carboxylic Acid-59: 4-methyl-5-(2,2,3,3-tetrafluoropropoxy)picolinic acid

(331) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.43 (1H, s), 7.92 (1H, s), 6.71 (1H, tt, J=51.6, 5.5 Hz), 4.86 (2H, t, J=13.0 Hz), 2.24 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 268 (M+H).sup.+.

Carboxylic Acid-60: 5-methyl-6-(2-(trifluoromethoxy)ethoxy)nicotinic acid

(332) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 13.03 (1H, br s), 8.55 (1H, s), 8.04 (1H, s), 4.65-4.57 (2H, m), 4.47-4.42 (2H, m), 2.19 (3H, s), MS (ESI) m/z: 266 (M+H).sup.+.

Carboxylic Acid-61: 5-methyl-6-((2,2,2-trifluoroethoxy)methyl)nicotinic acid

: diethyl 3-methylpyridine-2,5-dicarboxylate

(333) The title compound is prepared in 72% yield (2.05 g, a yellow oil) from 2,5-dibromo-3-methylpyridine (3.00 g, 12.0 mmol) in a similar manner to Step-2 of Carboxylic acid-47.

(334) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 9.10 (1H, d, J=1.5 Hz), 8.21 (1H, s), 4.52-4.39 (4H, m), 2.62 (3H, s), 1.48-1.40 (6H, m), MS (ESI) m/z: 238 (M+H).sup.+.

: ethyl 6-(hydroxymethyl)-5-methylnicotinate

(335) To a mixture of diethyl 3-methylpyridine-2,5-dicarboxylate (2.05 g, 8.63 mmol, Step-1) and calcium chloride (3.83 g, 34.5 mmol) in THF-EtOH (1:1, 50 mL) is added portionwise sodium borohydride (816 mg, 21.6 mmol) at 0 C. After stirring at rt for 18 hours, the reaction is carefully quenched with saturated ammonium chloride aqueous solution (300 mL), and the aqueous layer is extracted with DCM (300 mL). The separated organic layer is dried over sodium sulfate and concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with hexane/EtOAc (1:1) to give 1.25 g (74%) of the title compound as a pale yellow solid.

(336) .sup.1H-NMR (300 MHz, CDCl.sub.3) delta 9.02 (1H, s), 8.08 (1H, s), 4.74 (2H, s), 4.42 (2H, q, J=7.3 Hz), 2.28 (3H, s), 1.42 (3H, t, J=7.3 Hz), MS (ESI) m/z: 196 (M+H).sup.+.

: ethyl 6-(chloromethyl)-5-methylnicotinate hydrochloride

(337) To a solution of ethyl 6-(hydroxymethyl)-5-methylnicotinate (1.25 g, 6.40 mmol, Step-2) in DCM (25 mL) is added thionyl chloride (0.93 mL, 12.8 mmol) at 0 C. After stirring at rt for 1 hour, the solvent is removed in vacuo to give 1.37 g (quantitative yield) of the title compound as a pale yellow solid.

(338) MS (ESI) m/z: 214 (M+H).sup.+.

:5-methyl-6-((2,2,2-trifluoroethoxy)methyl)nicotinic acid

(339) To a mixture of 2,2,2-trifluoroethanol (3.84 g, 38.4 mmol) and cesium carbonate (8.33 g, 25.6 mmol) in DMF (20 mL) is added ethyl 6-(chloromethyl)-5-methylnicotinate hydrochloride (1.37 g, 6.39 mmol, Step-3). After stirring at 40 C. for 20 hours, 2 M aqueous sodium hydroxide solution (20 mL), water (20 mL), THF (20 mL), and EtOH (20 mL) are added to the mixture. After stirring at 60 C. for 3 hours, the mixture is acidified by 2 M hydrochloric acid (pH is around 4). The organic solvent is removed by evaporation, and the residual aqueous layer is extracted with EtOAc/hexane. The separated organic layer is washed with water, dried over sodium sulfate, and concentrated in vacuo. The residue is crystallized from hexane to give 1.06 g (66%) of the title compound as a white solid.

(340) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.85 (1H, d, J=1.5 Hz), 8.11 (1H, s), 4.84 (2H, s), 4.22-4.12 (2H, m), 2.40 (3H, s) (a signal due to COOH is not observed), MS (ESI) m/z: 248 (MH).sup..

Carboxylic Acid-62: 6-(4,4-difluoropiperidin-1-yl)-5-methylnicotinic acid

(341) A mixture of methyl 6-fluoro-5-methylnicotinate (2.00 g, 11.8 mmol), 4,4-difluoropiperidine hydrochloride (4.66 g, 29.6 mmol), and cesium carbonate (13.5 g, 41.4 mmol) in DMF is stirred at 120 C. for 16 hours. After cooling to rt, 1 M aqueous sodium hydroxide solution (50 mL) and MeOH (50 mL) are added to the resulting mixture. After stirring at 60 C. for 3 hours, the mixture is acidified by 2 M hydrochloric acid (pH is around 4), and MeOH is removed in vacuo. The formed white precipitate is collected by filtration to give 1.17 g (39%) of the title compound as a white solid.

(342) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 8.60 (1H, s), 7.95 (1H, s), 3.60-3.20 (4H, m), 2.30 (3H, s), 2.19-2.02 (4H, m), MS (ESI) m/z: 257 (M+H).sup.+.

Example Synthesis Part

Example 5: 5-methyl-N-((2-propionamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide

(343) To a mixture of N-(4-(aminomethyl)pyridin-2-yl)propionamide (20 mg, 0.11 mmol, Amine-2), 5-methyl-6-(2,2,2-trifluoroethoxy)nicotinic acid (29 mg, 0.12 mmol, Carboxylic acid-1) and N,N-diisopropylethylamine (0.078 mL, 0.45 mmol) in DMF (0.5 mL) is added a solution of HBTU (51 mg, 0.13 mmol) in DMF (0.5 mL) at room temperature. After stirring at room temperature for 3 days, the mixture is diluted with EtOAc (6 mL), washed with water, and dried over sodium sulfate. The organic layer is purified by column chromatography on NH-silica gel eluting with EtOAc and then by preparative LC-MS to give 3.6 mg of the title compound.

(344) Examples except for the alternative routes described below are prepared according to the procedure similar to that described in Example 5, using the appropriate amine and the carboxylic acid (see Table 1). The reactants are commercially available materials or obtained by conventional methods known to those skilled in the art, otherwise noted in the intermediate synthesis part.

(345) The procedures for the alternative route are described below.

Example 1: N-((2-acetamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide

: N-((2-aminopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxyl)nicotinamide

(346) To a stirred solution of 6-(2,2,2-trifluoroethoxy)nicotinic acid (300 mg, 1.36 mmol), 4-(aminomethyl)pyridin-2-amine (167 mg, 1.36 mmol), and N,N-diisopropylethylamine (0.95 mL, 5.43 mmol) in DMF (6 mL) is added HBTU (772 mg, 2.04 mmol) at room temperature. After stirring at 60 C. for 2 hours, the mixture is diluted with EtOAc (50 mL), washed with water (50 mL2), and dried over sodium sulfate. After removal of the solvent, the residue is purified by column chromatography on silica-gel eluting with DCM/MeOH (50:1-10:1) to give 330 mg (75%) of the title compound as a white solid.

(347) .sup.1H-NMR (300 MHz, DMSO-d.sub.6) delta 9.11 (1H, t, J=5.9 Hz), 8.74 (1H, d, J=2.2 Hz), 8.26 (1H, dd, J=8.8 and 2.2 Hz), 7.81 (1H, d, J=5.1 Hz), 7.11 (1H, d, J=8.8 Hz), 6.42 (1H, d, J=5.1 Hz), 6.34 (1H, s), 5.87 (2H, s), 5.08 (2H, q, J=8.8 Hz), 4.35 (1H, s), 4.33 (1H, s), MS (ESI) m/z: 327 (M+H).sup.+.

: N-((2-acetamidopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxy)nicotinamide

(348) To a stirred solution of N-((2-aminopyridin-4-yl)methyl)-6-(2,2,2-trifluoroethoxyl)nicotinamide (25 mg, 0.077 mmol, Step-1) and pyridine (0.037 mL, 0.46 mmol) in DMA (1 mL) is added acetyl chloride (0.016 mL, 0.23 mmol) at room temperature. After 1 hour, the mixture is diluted with EtOAc (3 mL), washed with water (3 mL), and dried over sodium sulfate. The organic layer is purified by column chromatography on NH-silica gel eluting with EtOAc and then by preparative LC-MS to give 6.9 mg of the title compound.

(349) MS (ESI) m/z: 367 (MH).sup..

(350) Examples 2, 3, 4, and 9 are prepared according to the procedure similar to that described in Example 1 using the appropriate acid chlorides.

Example 72: N-(4-(1-(3-(4-(trifluoromethoxy)phenyl)ureido)ethyl)pyridin-2-yl)isobutyramide (Single Enantiomer)

(351) A mixture of 1-isocyanato-4-(trifluoromethoxy)benzene (19 mg, 0.092 mmol) and N-(4-(1-aminoethyl)pyridin-2-yl)isobutyramide hydrochloride (single enantiomer) (15 mg, 0.062 mmol, Amine-12), and N,N-diisopropylethylamine (0.021 mL, 0.12 mmol) in DMA is stirred at 60 C. for 2 hours. After cooling to rt, the mixture is diluted with EtOAc (3 mL), washed with water (3 mL), dried over sodium sulfate, and concentrated. The residue is diluted with MeOH (4 mL) and applied onto a strong cation exchange cartridge (BondElute SCX, 1 g/6 mL, Varian Inc.), and the solid phase matrix is rinsed with MeOH (5 mL). The crude mixture is eluted with 1M ammonia in MeOH (5 mL) and concentrated. This is purified by preparative LC-MS to give 15.4 mg (61% yield) of the title compound.

(352) MS (ESI) m/z: 411 (M+H).sup.+.

(353) Examples 164, 165, and 166 are prepared according to the procedure similar to that described in Example 72. Example 164 is prepared from 1-isocyanato-3-(trifluoromethyl)benzene and N-(4-(1-aminoethyl)pyridin-2-yl)isobutyramide hydrochloride (single enantiomer) (Amine-12). Example 165 is prepared from 1-isocyanato-4-(trifluoromethyl)benzene and N-(4-(1-aminoethyl)pyridin-2-yl)isobutyramide hydrochloride (single enantiomer) (Amine-12). Example 166 is prepared from 1-isocyanato-4-(trifluoromethoxy)benzene and N-(4-(1-aminoethyl)-6-methylpyridin-2-yl)acetamide hydrochloride (single enantiomer) (Amine-8).

Example 180: N-(1-(2-isobutyramidopyridin-4-yl)ethyl)-6-(trifluoromethyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide (Single Enantiomer)

(354) A mixture of N-(4-(1-aminoethyl)pyridin-2-yl)isobutyramide hydrochloride (20 mg, 0.082 mmol, Amine-12), 4-nitrophenyl chloroformate (18 mg, 0.090 mmol), and triethylamine (0.034 mL, 0.25 mmol) in DCM (1 mL) is stirred at rt for 1 hour. Then, 6-(trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride (20 mg, 0.082 mmol) and DBU (25 mg, 0.16 mmol) are added. After stirring at rt, the mixture is diluted with EtOAc (3 mL), washed with water (3 mL), dried over sodium sulfate, and concentrated. The residue is diluted with MeOH (4 mL) and applied onto a strong cation exchange cartridge (BondElute SCX, 1 g/6 mL, Varian Inc.), and the solid phase matrix is rinsed with MeOH (5 mL). The crude mixture is eluted with 1M ammonia in MeOH (5 mL) and concentrated. This is purified by preparative LC-MS to give 9.4 mg (26% yield) of the title compound.

(355) MS (ESI) m/z: 435 (M+H).sup.+.

(356) The observed MS (positive or negative mode) and retention time by LC-MS of all examples are described in Table 2. Each chemical structure of Amine part for synthesis of Example is described as a free-base in Table 1. .sup.1H-NMR of Example 31, 61, and 149 are described in Table 3.

(357) TABLE-US-00002 TABLE 1 carboxylic acid Ex Structure Name part amine part 1 0 N-((2-acetamidopyridin- 4-yl) methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide alternative route 2 N-((2-propionamidopyridin- 4-yl)methyl)-6- (2,2,2-trifluoroethoxy) nicotinamide alternative route 3 N-((2-(cyclo- propanecarboxamido) pyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide alternative route 4 N-((2-benzamidopyridin- 4-yl) methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide alternative route 5 5-methyl-N-((2- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 6 5-chloro-N-((2- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 7 0 N-((2- propionamidopyridin- 4-yl)methyl)-4- (2,2,2-trifluoroethoxy) benzamide 8 N-((2- isobutyramidopyridin- 4-yl)methyl)-6- (2,2,2-trifluoroethoxy) nicotinamide 9 N-((2- (cyclobutanecarboxamido) pyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide alternative route 10 N-((2- propionamidopyridin- 4-yl)methyl)-6- (3,3,3-trifluoropropxoy) nicotinamide 11 0 2-methoxy-N-((2- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 12 N-((2-methyl-6- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 13 5-methyl-N-((2-methyl-6- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 14 5-chloro-N-((2-methyl-6- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 0 15 5-fluoro-N-((2-methyl-6- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 16 N-((2- (cyclopropane- carboxamido) pyridin-4- yl)methyl)-6-(3,3,3- trifluoropropoxy) nicotinamide 17 4-methyl-N-((2-methyl-6- propionamidopyridin-4- yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 0 18 2-methoxy-N-((2- methyl-6- propionamidopyridin- 4-yl)methyl)-6-(2,2,2- trifluoroethoxy) nicotinamide 19 N-((2- propionamidopyridin- 4-yl)methyl)-5- (2,2,2-trifluoroethoxy) picolinamide 20 N-((2-methyl-6- propionamidopyridin-4- yl)methyl)-5-(2,2,2- trifluoroethoxy) picolinamide 21 0 N-(1-(2- acetamidopyridin-4-yl) ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 22 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 23 N-(1-(2-(cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 24 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 0 25 N-(1-(2- acetamidopyridin- 4-yl) ethyl)-5-methyl-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 26 5-methyl-N-(1-(2- propionamidopyridin- 4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 27 N-(1-(2- (cyclopropane- carboxamido) pyridin-4-yl)ethyl)- 5-methyl-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 28 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methyl-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 29 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 30 N-(1-(2-methyl-6- propionamidopyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 31 0 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 32 N-(1-(2-isobutyramido-6- methylpyrimidin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 33 N-(1-(2-isobutyamido-6- methylpyrimidin-4- yl)ethyl)-5-methyl-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 34 N-(1-(2-acetamido-6- methylpyrimidin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 00 01 35 02 N-(1-(6-methyl-2- propionamidopyrimidin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 03 04 36 05 N-(1-(2- (cyclopropane- carboxamido)-6- methylpyrimidin-4-yl) ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 06 07 37 08 N-(1-(2-acetamido-6- methylpyrimidin-4-yl) ethyl)-5-methyl-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 09 0 38 N-(1-(2- (cyclopropane- carboxamido)- 6-methylpyrimidin-4-yl) ethyl)-5-methyl-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 39 5-methyl-N-(1- (6-methyl-2- propionamidopyrimidin- 4-yl) ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 40 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 41 0 N-(1-(2-methyl-6- propionamidopyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 42 N-(1-(2- (cyclopropane- carboxamido)- 6-methylpyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 43 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 44 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-6- (3,3,3-trifluoropropyl) nicotinamide (single enantiomer) 0 45 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5-chloro-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 46 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 47 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5-methyl-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 0 48 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-2-methoxy-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 49 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 50 N-(1-(2-acetamido-6- methylpyridin-4- yl)ethyl)-4- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 51 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-4-(1,1,2,2- tetrafluoroethoxy) benzamide (single enantiomer) 52 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-3- chloro-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 53 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-4- (2,2-difluoroethoxy)- 3-methylbenzamide (single enantiomer) 54 N-(1-(2-acetamido-6- methylpyridin-4- yl)ethyl)-6- (2,2-difluoroethoxy)-5- methylnicotinamide (single enantiomer) 0 55 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- methyl-6-(2,2,3,3- tetrafluoropropoxy) nicotinamide (single enantiomer) 56 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- methoxy-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 57 6-(2,2-difluoroethoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methylnicotinamide (single enantiomer) 0 58 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (3,3,3-trifluoropropoxy) nicotinamide (single enantiomer) 59 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (2,2,3,3,3- pentafluoropropoxy) nicotinamide (single enantiomer) 60 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methyl-6-(2,2,3,3- tetrafluoropropoxy) nicotinamide (single enantiomer) 61 0 N-(1-(2- isobutyramidopyridin- 4-yl)ethy)-5- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 62 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 63 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- (1,1,2,2-tetrafluoroethoxy) benzamide (single enantiomer) 64 N-(1-(2- isobutyamidopyridin- 4-yl)ethyl)-4- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 0 65 N-(1-(2- isobutyamidopyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 66 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (3,3,3-trifluoropropyl) nicotinamide (single enantiomer) 67 N-(4-(1-(2-(4- (trifluoromethyl) phenyl)acetamido) ethyl)pyridin-2-yl) isobutyamide (single enantiomer) 00 68 01 N-(4-(1-(2-(4- (trifluoromethoxy) phenyl)acetamido) ethyl)pyridin- 2-yl)isobutyramide e(singlenantiomer) 02 03 69 04 N-(4-(1-(2-(4- (trifluoromethyl) phenoxy)acetamido) ethyl)pyridin- 2-yl)isobutyramide (single enantiomer) 05 06 70 07 N-(4-(1-(2-(2- (trilfuoromethyl) phenoxy)acetamido) ethyl)pyridin-2-yl) isobutyamide (single enantiomer) 08 09 71 0 N-(1-(2- isobutyamidopyridin- 4-yl)ethyl)-4- (perfluoroethoxy) benzamide (single enantiomer) 72 N-(4-(1-(3-(4- (trifluoromethoxy) phenyl) ureido)ethyl)pyridin-2- yl)isobutyramide (single enantiomer) alternative route 73 5-chloro-N-(1-(2- (cyclopropane- carboxamido) pyridin-4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 74 N-(1-(2- (cyclopropane- carboxamido) pyridin-4-yl)ethyl)- 5-fluoro-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 75 0 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-2-methoxy-6- (2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 76 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 77 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 78 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 0 79 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(3,3,3- trifluoropropyl) nicotinamide (single enantiomer) 80 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 81 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-3-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 0 82 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-4-(1,1,2,2- tetrafluoroethoxy) benzamide (single enantiomer) 83 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-5-methyl- 6-(2,2,3,3- tetrafluoropropoxy) nicotinamide (single enantiomer) 84 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,3,3,3- pentafluoropropoxy) nicotinamide (single enantiomer) 85 0 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 86 N-(4-(1-(2-(4- (trifluoromethyl) phenyl)acetamido) ethyl)pyridin-2- yl)cyclopropane- carboxamide (single enantiomer) 87 N-(4-(1-(2-(4- (trifluoromethyl) phenoxy) acetamido)ethyl) pyridin-2-yl) cyclopropane- carboxamide (single enantiomer) 88 N-(1-(2- (cyclopropane- carboxamido) pyridin-4-yl)ethyl)- 2-(1,1,1-trifluoro-2- methylpropan-2-yl) quinoline-6-carboxamide (single enantiomer) 0 89 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-5- (trifluoromethoxy)- 1H-indole-2- carboxamide (single enantiomer) 90 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6- (trifluoromethoxy)-1H- indazole-3- carboxamide (single enantiomer) 91 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 0 92 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-3- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 93 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-6- (2,2,3,3,3- pentafluoropropoxy) nicotinamide (single enantiomer) 94 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-4- (perfluoroethoxy) benzamide (single enantiomer) 95 0 N_(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-2- (4-(trifluoromethyl) phenoxy)acetamide (single enantiomer) 96 N-(1-(6-methyl-2- propionamido- pyrimidin- 4-yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 97 N-(1-(2- isobutyramido- 6-methylpyrimidin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 98 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-5- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 0 99 5-chloro-N-(1-(2- propionamidopyridin- 4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 100 5-fluoro-N-(1-(2- propionamidopyridin- 4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 101 6-(2,2-difluoroethoxy)- 5-methyl-N-(1-(2- propionamidopyridin- 4-yl)ethyl) nicotinamide (single enantiomer) 00 102 01 2-methoxy-N-(1-(2- propionamidopyridin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 02 03 103 04 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-4- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 05 06 104 07 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-6- (3,3,3-trifluoropropoxy) nicotinamide (single enantiomer) 08 09 105 0 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-6- (3,3,3-trifluoropropyl) nicotinamide (single enantiomer) 106 4-(perfluoroethoxy)- N-(1-(2- propionamidopyridin- 4-yl)ethyl)benzamide (single enantiomer) 107 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-3- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 108 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-4- (1,1,2,2- tetrafluoroethoxy) benzamide (single enantiomer) 0 109 5-methyl-N-(1-(2- propionamidopyridin-4- yl)ethyl)-6-(2,2,3,3- tetrafluoropropoxy) nicotinamide (single enantiomer) 110 6-(2,2,3,3,3- pentafluoropropoxy)- N-(1-(2- propionamidopyridin- 4-yl)ethyl) nicotinamide (single enantiomer) 111 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 0 112 4-(2,2-difluoroethoxy)- 3-methyl-N-(1-(2- propionamidopyridin- 4-yl)ethyl)benzamide (single enantiomer) 113 N-(1-(2- (cyclopropane- carboxamido) pyridin-4-yl)ethyl)- 6-methyl-2-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 114 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-4-((2,2,2- trifluoroethoxy)methyl) benzamide (single enantiomer) 115 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-4-((2,2,2- trifluoroethoxy)methyl) benzamide (single enantiomer) 116 N-(1-(2-(3- methylbutanamido) pyridin-4-yl)ethyl)- 6-(2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 117 2-fluoro-N-(1-(2- isobutyramidopyridin-4- yl)ethyl)-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 118 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) pyridazine- 3-carboxamide (single enantiomer) 0 119 N-(1-(2-acetamido-6- methylpyrimidin-4- yl)ethyl)-2-methoxy-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 120 2-methoxy-N-(1- (6-methyl-2- propionamidopyrimidin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 121 N-(1-(2- (cyclopropane- carboxamido)-6- methylpyrimidin- 4-yl)ethyl)-2- methoxy-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 122 N-(1-(2-isobutyramido-6- methylpyrimidin-4- yl)ethyl)-2-methoxy- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 123 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- (3,3,3-trifluoropropoxy) picolinamide (single enantiomer) 124 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- (2,2,3,3,3- pentafluoropropoxy) picolinamide (single enantiomer) 125 0 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- (2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 126 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(4- (trifluoromethyl) phenoxy) propanamide (single enantiomer) 127 6-(2,2,3,3,3- pentafluoropropoxy)- N-(1-(2- propionamidopyridin- 4-yl)ethyl) pyridazine-3- carboxamide (single enantiomer) 128 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,3,3,3- pentafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 0 129 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (2,2,3,3,3- pentafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 130 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) pyridazine- 3-carboxamide (single enantiomer) 131 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 0 132 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 133 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-6- (2,2,3,3,3- pentafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 134 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-6-(2,2,3,3- tetrafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 135 00 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-6- (2,2,3,3- tetrafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 01 02 136 03 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,3,3- tetrafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 04 05 137 06 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (2,2,3,3- tetrafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 07 08 138 09 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 0 139 N-(1-(2- isobutyamidopyrimidin- 4-yl)ethyl)-2- methoxy-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 140 N-(1-(2- (cyclobutane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 141 N-(1-(2- acrylamidopyridin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enanitomer) 0 142 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- (3,3,3-trifluoropropoxy) benzamide (single enantiomer) 143 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methyl-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 144 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 4-(3,3,3- trifluoropropooxy) benzamide (single enantiomer) 145 0 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-3- (3,3,3-trifluoropropoxy) benzamide (single enantiomer) 146 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 5-methyl-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 147 N-(1-(2-methyl-6- propionamidopyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 148 N-(1-(2- (cyclopropane- carboxamido)- 6-methylpyridin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 0 149 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 150 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-3- methyl-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 151 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-3- methyl-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 0 152 5-(2,2,3,3,3- pentafluoropropoxy)- N-(1-(2- propionamidopyridin- 4-yl) ethyl)picolinamide (single enantiomer) 153 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-5-(2,2,3,3,3- pentafluoropropoxy) picolinamide (single enantiomer) 154 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5-(2,2,3,3,3- pentafluoropropoxy) picolinamide (single enantiomer) 155 0 N-(1-(2- propionamidopyridin- 4-yl)ethyl)-5- (2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 156 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-5-(2,2,3,3- tetrafluoropropxoy) picolinamide (single enantiomer) 157 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-5- (2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 158 N-(1-(2- (cyclobutane- carboxamido) pyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 0 159 N-(1-(2- acrylamidopyridin- 4-yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 160 N-(1-(2- (cyclohexane- carboxamido) pyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enntiomer) 161 N-(1-(2- pivalamidopyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 0 162 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 163 N-(1-(2- butyramidopyridin- 4-yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 164 N-(4-(1-(3-(3- (trifluoromethyl) phenyl)ureido) ethyl)pyridin-2- yl)isobutyramide (single enantiomer) alternative route 165 N-(4-(1-(3-(4- (trifluoromethyl) phenyl)ureido) ethyl)pyridin-2- yl)isobutyramide (single enantiomer) alternative route 166 N-(6-methyl-4-(1-(3-(4- (trifluoromethoxy) phenyl)ureido) ethyl)pyridin-2- yl)acetamide (single enantiomer) alternative route 167 0 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-2-methoxy- 6-(2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 168 N-(1-(2- (cyclobutane- carboxamido) pyridin-4- yl)ethyl)-2-methoxy- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 169 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-6- (2,2-difluoropropoxy) nicotinamide (single enantiomer) 170 6-(2,2-difluoropropoxy)- N-(1-(2- propionamidopyridin- 4-yl) ethyl)nicotinamide (single enantiomer) 00 01 171 02 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2- difluoropropoxy) nicotinamide (single enantiomer) 03 04 172 05 6-(2,2-difluoropropoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl) nicotinamide (single enantiomer) 06 07 173 08 2-hydroxy-N-(1-(2- isobutyramidopyridin-4- yl)ethyl)-4- (trifluoromethyl) benzamide (single enantiomer) 09 0 174 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- methoxy-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 175 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-2-methoxy- 6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 176 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-2- methoxy-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 177 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-6- (2,2-difluoroethoxy)- 2-methoxynicotinamide (single enantiomer) 178 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-(2,2- difluoroethoxy)-2- methoxynicotinamide (single enantiomer) 179 6-(2,2-difluoroethoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- methoxynicotinamide (single enantiomer) 180 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (trifluoromethyl)-3,4- dihydroisoquinoline- 2(1H)-carboxamide (single enantiomer) alternative route 181 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-1- methyl-5-(2,2,2- trifluoroethoxy)- 1H-pyrazole-3- carboxamide (single enantiomer) 182 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-6-methyl-5- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 183 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-6-methyl- 5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 184 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- methyl-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 0 185 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 186 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-methyl- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 187 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-2-methoxy-6- (2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 188 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-6-methyl- 5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 189 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-(2,2,3,3,3- pentafluoropropoxy) picolinamide (single enantiomer) 190 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-(2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 191 0 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 192 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-methyl- 6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 193 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-6-(3,3,3- trifluoropropyl) nicotinamide (single enantiomer) 194 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-6-(2,2,3,3,3- pentafluoropropoxy) nicotinamide (single enantiomer) 0 195 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-5-methyl-6- (2,2,3,3- tetrafluoropropoxy) nicotinamide (single enantiomer) 196 6-(2,2-difluoroethoxy)-N- (1-(2-isobutyramido-6- methylpyridin-4-yl)ethyl)- 2-methoxynicotinamide (single enantiomer) 197 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-2-methoxy-6- (3,3,3-trifluoro- propxy)nicotinamide (single enantiomer) 0 198 6-(2,2-difluoropropoxy)- N-(1-(2-isobutyramido- 6-methylpyridin-4-yl) ethyl) nicotinamide (single enantiomer) 199 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-6-(2,2,3,3,3- pentafluoropropoxy) pyridazine- 3-carboxamide (single enantiomer) 200 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 201 0 2-fluoro-N-(1-(2- isobutyramido- 6-methylpyridin- 4-yl)ethyl)-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 202 N-(1-(2- isobutyramido-6- methylpyridin-4- yl)ethyl)-3-methyl-4- (2,2,2- trifluoroethoxy) benzamide (single enantiomer) 203 3-chloro-N-(1-(2- isobutyramido- 6-methylpyridin- 4-yl)ethyl)-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 204 4-(2,2-difluoroethoxy)- N-(1-(2-isobutyramido- 6-methylpyridin-4-yl) ethyl)-3-methylbenzamide (single enantiomer) 00 01 205 02 N-(1-(2- isobutyramido-6- methylpyridin-4-yl) ethyl)-4-(3,3,3- trifluoropropoxy) benzamide (single enantiomer) 03 04 206 05 N-(1-(2- isobutyramido-6- methylpyridin-4- yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 06 07 207 08 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-4- (perfluoroethoxy) benzamide (single enantiomer) 09 0 208 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-2- (piperidin-1-yl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 209 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- (piperidin-1-yl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 210 N-(1-(2-acetamido-6- methylopyridin-4-yl)ethyl)- 2-morpholin-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 211 0 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- moprholin-6-(2,2,2- trifluoroethoxy) (single enantiomer) 212 N-(1-(2-isobutyramido- 6-methylpyridin-4-yl) ethyl)-2-morpholin- 6-(2,2,2-trifluoro- ethoxy)nicotinamide (single enantiomer) 213 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-2-(4- methoxypiperidin-1-yl)- 6-(2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 214 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(4- methoxypiperidin-1-yl)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 215 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-2-(4- methoxypiperidin- 1-yl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 216 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 2-((2-methoxyethyl) (methyl)amino)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enanitomer) 217 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-((2- methoxyethyl)(methyl) amino)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 218 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 2,6-bis(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 219 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2,6-bis (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 220 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-2,6-bis(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 221 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-2-(2- methoxyethoxy)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 222 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(2- methoxyethoxy)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 223 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-2-(2- methoxyethoxy)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 224 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)-2- (2,2-difluoroethoxy)- 6-(2,2,2- trilfuoroethoxy) nicotinamide (single enantiomer) 0 225 2-(2,2-difluoroethoxy)- N-(1-(2- isobutyramidopyridin-4-yl) ethyl)-6-(2,2,2- trifluoroethoxy)nicotinamide (single enantiomer) 226 2-(2,2-difluoroethoxy)-N- (1-(2-isobutyramido-6- methylpyridin-4-yl)ethyl)- 6-(2,2,2- trifluoroethoxy)nicotinamide (single enantiomer) 227 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)-3- methoxy-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 0 228 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-3- methoxy-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 229 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-3-methoxy-4- (2,2,2- trifluoroethoxy)benzamide (single enantiomer) 230 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 2-hydroxy- 4-(trifluoromethyl) benzamide (single enantiomer) 231 0 2-hydroxy-N-(1-(2- isobutyramido-6- methylpyridin-4-yl)ethyl)- 4-(trifluoromethyl) benzamide (single enantiomer) 232 2-hydroxy-N-(1-(2- isobutyramidopyridin-4- yl)ethyl)-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 233 2-hydroxy-N-(1-(2- isobutyramido-6- methylpyridin-4-yl)ethyl)- 4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 234 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-2-(4- fluorophenoxy)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 235 2-(4-fluorophenoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 236 2-(4-fluorophenoxy)-N-(1- (2-isobutyramido-6- methylpyridin-4-yl)ethyl)- 6-(2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 237 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-2-methoxy-4- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 00 238 01 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- methoxy-4-(2,2,2- trifluoroethoxy) benzamide (single enantiomer) 02 03 239 04 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-2-methoxy-4- (2,2,2-trifluoroethoxy) benzamide (single enantiomer) 05 06 240 07 N-(1-(2- (cyclopropane- carboxamido)- 6-methoxypyridin- 4-yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantomer) 08 09 241 0 N-(1-(2-isobutyramido-6- methoxypyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 242 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- ((2,2,2-trifluoroethoxy) methyl) benzamide (single enantiomer) 243 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-4-((2,2,2- trifluoroethoxy)methyl) benzamide (single enantiomer) 244 N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 2-methoxy-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 245 N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 5-(2,2,3,3,3- pentafluoropropoxy) picolinamide (single enantiomer) 246 N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 2-(piperidin-1-yl)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 247 N-(1-(2-(2-hydroxy- 2-methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 2-morpholino-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 248 2-(4-fluorophenoxy)- N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 6-(2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 249 N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 2-(2-methoxyethoxy)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 250 N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 2,6-bis(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 251 0 2-(2,2-difluoroethoxy)- N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl)ethyl)- 6-(2,2,2-trilfuoroethoxy) nicotinamide (single enantiomer) 252 N-(1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl) ethyl)-2-(4- (trifluoromethyl)phenyl) thiazole-4-carboxamide (single enantiomer) 253 3-chloro-N-(1-(2- isobutyramidopyridin-4- yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 254 3-chloro-N-(1-(2- isobutyramido-6- methylpyridin- 4-yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 0 255 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-3- chloro-4- (trifluoromethoxy) benzamide (single enantiomer) 256 N-(1-(2-acetamido-6- methylpyridin-4- yl)ethyl)-2-hydroxy- 4-(2,2,2-trifluoroethoxy) benzamide (single enantiomer) 257 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(4- methylpiperazin-1-yl)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 258 2-(4-hydroxypiperidin- 1-yl)-N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 259 2-(4-hydroxypiperidin- 1-yl)-N-(1-(2- isobutyramido-6- methylpyridin- 4-yl)ethyl)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 260 2-(4-fluorophenyl)-N- (1-(2-isobutyramido-6- methylpyridin-4-yl)ethyl)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 261 0 N-(1-(2-acetamido-6- methylpyridin-4- yl)ethyl)-2-(4- fluorophenyl)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 262 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(3- methoxypropoxy)- 6-(2,2,2-trifluoro- ethoxy)nicotinamide (single enantiomer) 263 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-2-(3- methoxypropoxy)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 264 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-2-(3- methoxypropoxy)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 265 2-hydroxy-N- (1-(2-(2-hydroxy-2- methylpropanamido)-6- methylpyridin-4-yl) ethyl)- 4-(2,2,2-trifluoroethoxy) benzamide (single enantiomer) 266 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-6-(2,2,3,3- tetrafluoropropoxy) pyridazine- 3-carboxamide (single enantiomer) 267 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(2-(2- oxopyrrolidin-1-yl) ethoxy)-6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 0 268 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-2-(2-(2- oxopyrrolidin- 1-yl)ethoxy)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 269 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 1-methyl-5-(2,2,3,3,3- pentafluoropropoxy)-1H- pyrazole-3-carboxamide (single enantiomer) 270 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-1-methyl- 5-(2,2,3,3,3- pentafluoropropoxy)- 1H-pyrazole-3- carboxamide (single enantiomer) 271 00 1-methyl-5-(2,2,3,3,3- pentafluoropropoxy)-N- (1-(2-propionamido- pyridin- 4-yl)ethyl)-1H-pyrazole- 3-carboxamide (single enantiomer) 01 02 272 03 N-(1-(2-acetamido-6- methylpyridin-4- yl)ethyl)-2- methoxy-4- (trifluoromethoxy) benzamide (single enantiomer) 04 05 273 06 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2- methoxy-4- (trifluoromethoxy) benzamide (single enantiomer) 07 08 274 09 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-2-methoxy-4- (trifluoromethoxy) benzamide (single enantiomer) 0 275 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-2- hydroxy-4- (trifluoromethoxy) benzamide (single enantiomer) 276 2-hydroxy-N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 277 2-hydroxy-N-(1-(2- isobutyramido-6- methylpyridin- 4-yl)ethyl)-4- (trifluoromethoxy) benzamide (single enantiomer) 0 278 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-2-(2- morpholinoethoxy)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 279 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-2-(2- morpholinoethoxy)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 280 N-(1-(2-acetamido- 6-methylpyridin- 4-yl)ethyl)-2- (2-morpholinoethoxy)- 6-(2,2,2- trifluoroethoxy) nicotinamide (single enantiomer) 281 0 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-3- fluoro-4- (trifluoromethoxy) benzamide (single enantiomer) 282 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- methyl-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 283 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methyl-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 284 N-(1-(2-isobutyramido- 6- methylpyridin-4- yl)ethyl)-5-methyl-6- (2,2,2-trifluoro- ethoxy)pyridazine-3- carboxamide (single enantiomer) 0 285 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-5-methyl- 6-(2,2,2-trifluoro- ethoxy)pyridazine-3- carboxamide (single enantiomer) 286 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-4- methyl-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 287 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- methyl-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 0 288 N-(1-(2-isobutyramido-6- methylpyridin-4-yl) ethyl)-4-methyl-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 289 N-(1-(2- (cyclopropane- carboxamido) pyridin-4- yl)ethyl)-4-methyl- 5-(2,2,2-trifluoro- ethoxy)picolinamide (single enantiomer) 290 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-4-methyl-5- (2,2,2-trifluoroethoxy) picolinamide (single enantiomer) 291 0 4-methyl-N-(1-(2- propionamidopyridin-4- yl)ethyl)-5-(2,2,2- trifluoroethoxy) picolinamide (single enantiomer) 292 5-methyl-N-(1-(2- propionamidopyridin-4- yl)ethyl)-6-(2,2,2- trifluoroethoxy) pyridazine-3- carboxamide (single enantiomer) 293 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-methyl-6- (2,2,2-trifluoroethoxy) pyridazine- 3-carboxamide (single enantiomer) 294 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-6- methyl-5-(2,2,2- trifluoroethoxy) pyrazine-2- carboxamide (single enanitomer) 0 295 N-(1-(2-isobutyramido-6- methylpyridin-4- yl)ethyl)-6-methyl- 5-(2,2,2-trifluoro- ethoxy)pyrazine-2- carboxamide (single enantiomer) 296 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-5- methyl-6-((2,2,2- trifluoroethyl)amino) nicotinamide (single enantiomer) 297 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- methyl-6-(2-(2,2,2- trifluoroethoxy)ethoxy) nicotinamide (single enantiomer) 0 298 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-methyl- 6-(2-(2,2,2- trifluoroethoxy)ethoxy) nicotinamide (single enantiomer) 299 N-(1-(2-acetamido-6- methylpyridin-4- yl)ethyl)-6- (2,2-difluoropropoxy)- 5-methylnicotinamide (single enantiomer) 300 6-(2,2-difluoropropoxy)- N-(1-(2-isobutyramido- 6-methylpyridin- 4-yl)ethyl)- 5-methylnicotinamide (single enantiomer) 301 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- (2,2-difluoroethoxy)-4- methylpicolinamide (single enantiomer) 302 5-(2,2-difluoroethoxy)-N- (1-(2-isobutyramido-6- methylpyridin-4-yl)ethyl)- 4-methylpicolinamide (single enantiomer) 303 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-4- methyl-5-(3,3,3- trifluoropropoxy) picolinamide (single enantiomer) 304 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-4-methyl- 5-(3,3,3- trifluoropropoxy) picolinamide (single enantiomer) 00 01 305 02 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-3-methyl- 4-(trifluoromethoxy) benzamide (single enantiomer) 03 04 306 05 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-3-methyl-4- (trifluoromethoxy) benzamide (single enantiomer) 06 07 307 08 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-1- (2,2,2-trifluoroethoxy) isoquinoline-4- carboxamide (single enantiomer) 09 0 308 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 5-methyl-6-((2,2,2- trifluoroethoxy)methyl) nicotinamide (single enantiomer) 309 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- methyl-6-(3,3,3- trifluoropropyl) nicotinamide (single enantiomer) 310 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-methyl- 6-(3,3,3- trifluoropropyl) nicotinamide (single enantiomer) 311 0 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- chloro-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 312 5-chloro-N-(1-(2- isobutyramido- 6-methylpyridin- 4-yl)ethyl)-6-(3,3,3- trifluoropropoxy) nicotinamide (single enantiomer) 313 N-(1-(2-acetamido-6- methylpyridin-4-yl)ethyl)- 5-chloro-6-(2,2- difluoropropoxy) nicotinamide (single enantiomer) 314 5-chloro-6-(2,2- difluoropropoxy)- N-(1-(2- isobutyramido-6- methylpyridin-4- yl)ethyl)nicotinamide (single enantiomer) 0 315 N-(1-(2-acetamido-6- methylpyridin- 4-yl)ethyl)-6- ((4-fluorobenzyl)oxy)-5- methylnicotinamide (single enantiomer) 316 6-((4-fluorobenzyl)oxy)- N-(1-(2-isobutyramido-6- methylpyridin-4-yl) ethyl)- 5-methylnicotinamide (single enantiomer) 317 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-4- methyl-5-(2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 0 318 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-4-methyl- 5-(2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 319 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-6-(4,4- difluoropiperidin-1-yl)- 5-methylnicotinamide (single enantiomer) 320 6-(4,4-difluoropiperidin- 1-yl)-N-(1-(2- isobutyramido- 6-methylpyridin- 4-yl)ethyl)-5- methylnicotinamide (single enantiomer) 321 0 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-methyl-6- (2,2,3,3- tetrafluoropropoxy) nicotinamide (single enantiomer) 322 N-(1-(2-acetamidopyridin- 4-yl)ethyl)-5- (2,2,3,3,3- pentafluoropropoxy) picolinamide (single enantiomer) 323 N-(1-(2- acetamidopyridin-4- yl)ethyl)-6-methyl-5- (2,2,2-trifluoroethoxy) pyrazine-2-carboxamide (single enantiomer) 324 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-6-(2,2- difluoropropoxy)-5- methylnicotinamide (single enantiomer) 0 325 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-chloro-6- (3,3,3-trifluoropropoxy) nicotinamide (single enantiomer) 326 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-6- (trifluoromethyl)-1H- benzo[d]imidazole-2- carboxamide (single enantiomer) 327 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-6-((4- fluorobenzyl)oxy)-5- methylnicotinamide (single enantiomer) 0 328 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- methyl-5-(2,2,2- trifluoroethoxy)pyrazine-2- carboxamide (single enantiomer) 329 6-(2,2-difluoropropoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methylnicotinamide (single enantiomer) 330 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-6- (trifluoromethyl)-1H- benzo[d]imidazole-2- carboxamide (single enantiomer) 331 0 6-((4-fluorobenzyl)oxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methylnicotinamide (single enantiomer) 332 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- methyl-5-(2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 333 N-(1-(2-acetamidopyridin- 4-yl)ethyl)-5-(2,2- difluoroethoxy)-4- methylpicolinamide (single enantiomer) 334 5-(2,2-difluoroethoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)- 4-methylpicolinamide (single enantiomer) 0 335 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-4-methyl-5- (3,3,3-trifluoropropoxy) picolinamide (single enantiomer) 336 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- methyl-5-(3,3,3- trifluoropropoxy) picolinamide (single enantiomer) 337 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-methyl-6- (3,3,3-trifluoropropoxy) nicotinamide (single enantiomer) 000 338 001 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-2-(4- fluorophenoxy)-6- (2,2,2-trifluoroethoxy) nicotinamide (single enantiomer) 002 003 339 004 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-4-methyl-5- (2,2,3,3- tetrafluoropropoxy) picolinamide (single enantiomer) 005 006 340 007 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-methyl-6- (2,2,3,3- tetrafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 008 009 341 010 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- methyl-6-(2,2,3,3- tetrafluoropropoxy) pyridazine- 3-carboxamide (single enantiomer) 011 012 342 013 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5- methyl-6-(2,2,3,3- tetrafluoropropoxy) pyridazine- 3-carboxamide (single enantiomer) 014 015 343 016 N-(1-(2-isobutyramido- 6-methylpyridin-4- yl)ethyl)-5-methyl- 6-(2,2,3,3- tetrafluoropropoxy) pyridazine-3- carboxamide (single enantiomer) 017 018 344 019 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-((4- fluorobenzyl)oxy)-4- methylpicolinamide (single enantiomer) 020 021 345 022 N5-((4-fluorobenzyl) oxy)-N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- methylpicolinamide (single enantiomer) 023 024 346 025 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-(2,2- difluoropropoxy)-4- methylpicolinamide (single enantiomer) 026 027 347 028 N-(1-(2-acetamido-6- methylpyridin-4-yl) ethyl)-5- (2,2-difluoropropoxy)- 4-methylpicolinamide (single enantiomer) 029 030 348 031 5-(2,2-difluoropropoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-4- methylpicolinamide (single enantiomer) 032 033 349 034 5-(2,2-difluoropropoxy)- N-(1-(2-isobutyramido- 6-methylpyridin-4-yl) ethyl)- 4-methylpicolinamide (single enantiomer) 035 036 350 037 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-5-methyl-6- (2-(trifluoromethoxy) ethoxy) nicotinamide (single enantiomer) 038 039 351 040 N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-5-methyl-6- (2-(trifluoro- methoxy)ethoxy) nicotinamide (single enantiomer) 041 042 352 043 N-(1-(2- isobutyramido-6- methylpyridin-4- yl)ethyl)-5-methyl-6-(2- (trifluoromethoxy) ethoxy) nicotinamide (single enantiomer) 044 045 353 046 N-(1-(2- isobutyramido-6- methylpyridin-4- yl)ethyl)-5-methyl-6- (trifluoromethyl) nicotinamide (single enantiomer) 047 048 354 049 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-4-(2,2- difluoropropoxy)-3- methylbenzamide (single enantiomer) 050 051 355 052 4-(2,2- difluoropropoxy)- N-(1-(2- isobutyramidopyridin- 4-yl)ethyl)-3- methylbenzamide (single enantiomer) 053 054 356 055 4-(2,2-difluoropropoxy)- N-(1-(2-isobutyramido- 6-methylpyridin- 4-yl)ethyl)- 3-methylbenzamide (single enantiomer) 056 057 357 058 N-(1-(2- acetamidopyridin- 4-yl)ethyl)-3-chloro-4- (2,2-difluoropropoxy) benzamide (single enantiomer) 059 060 358 061 3-chloro-4-(2,2- difluoropropoxy)- N-(1-(2-iso- butyramidopyridin-4-yl) ethyl)benzamide (single enantiomer) 062 063 359 064 3-chloro-4-(2,2- difluoropropoxy)- N-(1-(2- isobutyramido-6- methylpyridin-4- yl)ethyl)benzamide (single enantiomer) 065 066

(358) TABLE-US-00003 TABLE 2 Ex tR (min) m/z 1 1.38 367.3 2 1.47 381.3 3 1.51 393.3 4 1.63 429.2 5 1.57 395.2 6 1.60 415.1 7 1.47 380.2 8 1.55 395.2 9 1.59 407.2 10 1.47 395.2 11 1.60 411.2 12 1.53 395.2 13 1.62 409.2 14 1.65 429.1 15 1.58 413.2 16 1.50 407.3 17 1.57 409.3 18 1.66 425.2 19 1.47 381.3 20 1.53 395.2 21 1.43 381.2 22 1.52 395.2 23 1.59 409.1 24 1.62 411.1 25 1.54 395.2 26 1.62 409.3 27 1.65 421.3 28 1.69 423.3 29 1.52 395.3 30 1.62 409.2 31 1.70 423.3 32 1.59 424.3 33 1.70 438.3 34 1.45 396.3 35 1.53 410.4 36 1.55 422.3 37 1.55 410.4 38 1.66 436.4 39 1.63 424.3 40 1.52 395.3 41 1.60 409.3 42 1.63 421.3 43 1.68 423.3 44 1.41 393.3 45 1.64 429.3 46 1.51 409.3 47 1.61 409.3 48 1.66 425.3 49 1.57 380.3 50 1.51 394.3 51 1.55 412.3 52 1.61 428.2 53 1.51 390.3 54 1.50 391.3 55 1.61 441.3 56 1.76 441.1 57 1.60 407.1 58 1.61 425.1 59 1.74 461.0 60 1.70 457.1 61 1.63 411.1 62 1.68 396.0 63 1.64 428.0 64 1.61 410.0 65 1.72 411.1 66 1.52 409.1 67 1.62 394.1 68 1.66 410.1 69 1.68 410.1 70 1.69 410.1 71 1.81 446.0 72 1.69 411.1 73 1.71 443.0 74 1.64 427.0 75 1.74 439.1 76 1.60 409.1 77 1.59 408.1 78 1.58 423.1 79 1.49 407.1 80 1.69 409.1 81 1.62 408.1 82 1.62 426.1 83 1.68 455.1 84 1.72 459.1 85 1.65 394.1 86 1.59 392.1 87 1.65 408.1 88 1.83 471.0 89 1.72 433.0 90 1.63 434.0 91 1.62 395.3 92 1.56 394.3 93 1.66 445.2 94 1.71 430.2 95 1.59 394.3 96 1.54 412.0 97 1.59 426.0 98 1.56 397.0 99 1.68 430.9 100 1.60 415.0 101 1.54 393.0 102 1.70 427.0 103 1.55 396.0 104 1.55 411.0 105 1.45 395.1 106 1.74 432.0 107 1.58 396.0 108 1.58 414.0 109 1.64 443.0 110 1.68 446.9 111 1.61 382.0 112 1.55 392.0 113 1.74 423.0 114 1.60 421.9 115 1.54 410.0 116 1.69 425.0 117 1.66 426.1 118 1.61 410.2 119 1.59 428.2 120 1.67 442.2 121 1.69 454.2 122 1.73 456.2 123 1.66 425.1 124 1.76 461.2 125 1.65 443.1 126 1.73 424.2 127 1.67 448.1 128 1.70 460.1 129 1.74 462.1 130 1.53 398.2 131 1.57 410.2 132 1.51 398.1 133 1.65 448.1 134 1.53 430.1 135 1.55 430.1 136 1.59 442.1 137 1.63 444.1 138 1.64 410.9 139 1.67 442.1 140 1.66 423.1 141 1.54 395.1 142 1.64 424.0 143 1.71 439.1 144 1.55 410.1 145 1.58 410.1 146 1.62 425.1 147 1.60 412.1 148 1.64 424.1 149 1.68 426.1 150 1.71 424.0 151 1.61 410.1 152 1.69 447.0 153 1.72 459.1 154 1.66 447.0 155 1.58 429.0 156 1.61 441.0 157 1.55 429.0 158 1.67 423.1 159 1.55 395.1 160 1.81 451.1 161 1.74 425.1 162 1.47 383.1 163 1.63 411.1 164 1.66 395.2 165 1.66 395.2 166 1.59 397.1 167 1.61 413.1 168 1.81 453.1 169 1.48 392.2 170 1.50 393.2 171 1.54 405.1 172 1.58 407.1 173 1.72 396.1 174 1.78 455.1 175 1.75 453.0 176 1.68 441.0 177 1.57 409.1 178 1.63 421.1 179 1.67 423.1 180 1.69 435.1 181 1.40 400.1 182 1.54 397.1 183 1.67 423.1 184 1.71 424.7 185 1.78 425.1 186 1.76 439.1 187 1.82 455.1 188 1.78 439.1 189 1.81 475.1 190 1.69 457.1 191 1.66 439.1 192 1.75 453.2 193 1.57 423.1 194 1.79 475.1 195 1.75 471.1 196 1.72 437.2 197 1.84 469.2 198 1.62 421.1 199 1.79 476.1 200 1.65 424.1 201 1.71 442.1 202 1.75 438.1 203 1.75 458.1 204 1.65 420.2 205 1.68 438.1 206 1.72 410.2 207 1.85 459.3 208 1.87 480.1 209 1.97 494.1 210 1.58 482.1 211 1.68 496.1 212 1.75 510.1 213 1.69 510.1 214 1.80 523.4 215 1.86 538.1 216 1.64 484.1 217 1.74 498.2 218 1.74 495.0 219 1.83 509.1 220 1.89 523.1 221 1.66 471.1 222 1.77 485.1 223 1.83 499.1 224 1.67 477.0 225 1.77 491.0 226 1.83 505.1 227 1.49 426.1 228 1.59 440.1 229 1.65 454.1 230 1.60 382.1 231 1.78 410.1 232 1.71 426.0 233 1.78 440.1 234 1.81 507.0 235 1.91 520.3 236 1.96 535.1 237 1.58 426.1 238 1.68 440.1 239 1.74 454.1 240 1.71 439.1 241 1.75 441.1 242 1.61 423.5 243 1.67 438.1 244 1.70 471.1 245 1.69 491.0 246 1.91 524.1 247 1.63 526.1 248 1.86 551.1 249 1.71 515.1 250 1.78 539.1 251 1.72 521.1 252 1.82 493.0 253 1.78 430.0 254 1.85 444.0 255 1.68 416.0 256 1.61 412.0 257 1.57 508.9 258 1.58 510.0 259 1.64 524.1 260 1.84 519.1 261 1.69 491.1 262 1.82 498.3 263 1.88 513.2 264 1.71 485.1 265 1.66 456.1 266 1.67 458.1 267 1.60 536.3 268 1.65 550.4 269 1.54 448.4 270 1.70 476.4 271 1.56 448.3 272 1.63 412.1 273 1.74 426.1 274 1.80 440.1 275 1.66 398.1 276 1.75 412.1 277 1.83 426.1 278 1.70 540.2 279 1.76 554.3 280 1.59 526.2 281 1.60 400.1 282 1.55 412.2 283 1.66 426.2 284 1.72 440.2 285 1.62 424.1 286 1.57 411.2 287 1.67 425.1 288 1.73 439.2 289 1.63 423.1 290 1.50 397.0 291 1.59 411.1 292 1.58 412.1 293 1.49 398.2 294 1.59 412.1 295 1.76 440.2 296 1.36 410.1 297 1.54 455.2 298 1.69 483.2 299 1.53 407.2 300 1.69 435.2 301 1.46 393.1 302 1.63 421.1 303 1.59 425.1 304 1.75 453.1 305 1.62 396.1 306 1.78 423.8 307 1.64 447.1 308 1.39 425.1 309 1.47 409.1 310 1.63 437.1 311 1.61 444.7 312 1.76 473.1 313 1.58 427.1 314 1.73 455.1 315 1.68 437.0 316 1.83 465.1 317 1.57 443.0 318 1.73 471.0 319 1.51 432.1 320 1.67 460.2 321 1.51 429.0 322 1.56 432.9 323 1.52 398.0 324 1.47 393.0 325 1.55 430.9 326 1.45 392.0 327 1.62 423.0 328 1.69 426.0 329 1.63 421.0 330 1.61 420.0 331 1.77 451.0 332 1.67 457.0 333 1.40 379.0 334 1.57 407.0 335 1.53 411.0 336 1.69 439.0 337 1.51 411.0 338 1.73 492.9 339 1.51 429.0 340 1.50 429.9 341 1.55 444.0 342 1.66 458.0 343 1.72 472.0 344 1.65 423.0 345 1.80 451.0 346 1.48 393.2 347 1.54 407.2 348 1.65 421.2 349 1.71 435.2 350 1.54 427.2 351 1.69 455.2 352 1.75 469.2 353 1.61 409.2 354 1.49 392.3 355 1.64 420.3 356 1.70 434.3 357 1.51 412.2 358 1.65 440.2 359 1.71 454.2

(359) TABLE-US-00004 TABLE 3 Example salt data 31 free .sup.1H-NMR (CDCl.sub.3, 300 MHz) 8.30 (1H, d, J = 2.9 Hz), 8.16 (1H, d, J = 8.8 Hz), 8.20-8.13 (1H, m), 8.09 (1H, s), 7.79 (1H, br s), 7.34 (1H, dd, J = 8.8, 2.9 Hz), 6.91 (1H, s), 5.19 (1H, quintet, J = 7.3 Hz). 4.46 (2H, q, J = 7.3 Hz), 2.51 (1H, septet, J = 6.6 Hz), 2.42 (3H, s), 1.59 (3H, d, J = 6.6 Hz), 1.24 (6H, d, J = 7.3 Hz). 61 HCl .sup.1H-NMR (DMSO-d.sub.6, 300 MHz) 11.51 (1H, br s), 9.27 (1H, d, J = 8.1 Hz), 8.49 salt (1H, d, J = 2.9 Hz), 8.30 (1H, d, J = 5.8 Hz), 8.02 (1H, d, J = 8.8 Hz), 7.86 (1H, s), 7.71 (1H, dd, J = 8.8, 2.9 Hz), 7.40 (1H, d, J = 5.8 Hz), 5.17 (1H, quintet, J = 7.3 Hz), 5.01 (2H, q, J = 8.8 Hz), 2.77 (1H, septet, J = 6.6 Hz), 1.54 (3H, d, J = 7.3 Hz), 1.02 (6H, d, J = 7.3 Hz) (a signal due to HCl is not observed). 149 free .sup.1H-NMR (CDCl.sub.3, 300 MHz) 8.26 (1H, d, J = 8.8 Hz), 8.19 (1H, d, J = 8.1 Hz), 8.10 (1H, s), 7.82 (1H, br s), 7.25 (1H, d, J = 8.8 Hz), 6.90 (1H, s), 5.22 (1H, quintet, J = 6.6 Hz), 5.01 (2H, q, J = 8.1 Hz), 2.51 (1H, septet, J = 6.6 Hz), 2.42 (3H, s), 1.61 (3H, d, J = 7.3 Hz), 1.24 (6H, d, J = 6.6 Hz).

(360) Pharmacological Assays

(361) In Vitro Human Voltage Gated Sodium Channels Activity

(362) The inhibitory activities of compounds against voltage gated sodium channels are determined by methodology well known in the art.

(363) The ability of the amide derivatives of the formula (I) to inhibit the Na.sub.v1.3, Na.sub.v1.7 and Na.sub.v1.5 channels is measured by Fluorescence Resonance Energy Transfer (FRET) assay and electrophysiology assay described below.

(364) FRET Assay

(365) This screen is used to determine the effects of compounds on human Na.sub.v1.3, human Na.sub.v1.7, and human Na.sub.v1.5 channels, utilizing electrical field stimulation (EFS) system in 96-well plate format on FDSS (Hamamatsu Photonics) platform. The change of membrane potential is monitored with FRET dye pair, oxonol (DiSBAC2(3)) and coumarin (CC2-DMPE).

(366) Cell Maintenance:

(367) Each HEK293 cells expressing human Na.sub.v1.3 channels and HEK293 cells expressing human Na.sub.v1.5 channels are grown in T225 flasks, in a 5% CO.sub.2 humidified incubator to about 80% confluence. Media composition consists of Dulbecco's Modified Eagle Medium (high glucose), 10% FCS, 100 units/mL Penicillin, 100 microgram/mL Streptomycin and 500 microgram/mL Geneticin.

(368) CHO cells expressing human Na.sub.v1.7 channels are grown in T225 flasks, in a 5% CO.sub.2 humidified incubator to about 80% confluence. Media composition consists of HAM/F12 with Glutamax I, 10% FCS, 100 units/mL Penicillin and 100 microgram/mL Hygromycin.

(369) Protocol: Seed each cell lines (110.sup.5 cells/well) into poly-D-lysine coated 96-well plates prior to experimentation. Incubate at 37 C. in 5% CO.sub.2 for 24 hours. Wash each well with assay buffer (140 mM NaCl, 4.5 mM KCl, 10 mM D-Glucose, 2 mM CaCl.sub.2, 1 mM MgCl.sub.2, 10 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), pH 7.4 adjusted with NaOH) twice. Add 1st loading solution containing 10 microM CC2-DMPE and 0.06% Pluronic F-127 in assay buffer. Incubate the plate at rt in dark for 1 hour. Remove 1st loading solution and added 2nd loading solution containing 15 microM DiSBAC2(3), 0.555 mM VABSC-1 and 0.004% Pluronic F-127 in assay buffer. Place the plate under the dark at rt for 25 minutes. Add compound solutions into the assay plate. Set the assay plate in FDSS and placed an EFS device on the plate. Measure EFS-induced fluorescent response by FDSS.

(370) The data are analyzed and reported as normalized ratios of intensities measured at 440 nm. The process of calculating these ratios is performed as follows:

(371) $\begin{array}{cc}\begin{array}{c}\mathrm{FIR}=\mathrm{Fluorescence}\mathrm{Integration}\mathrm{Ratio}\\ =\mathrm{the}\mathrm{integral}\mathrm{of}\mathrm{the}\mathrm{ratio}\mathrm{normalized}\mathrm{by}\\ \mathrm{baseline}\left(\mathrm{before}\mathrm{EFS}\right)\end{array}\%\mathrm{inhibition}\left(\mathrm{abbreviated}\mathrm{as}\mathrm{Inh}.\right)=\left(1-\frac{\left(\begin{array}{c}\mathrm{FIR}\mathrm{of}\mathrm{each}\mathrm{well}-\\ \mathrm{median}\mathrm{FIR}\mathrm{in}100\%\mathrm{Inh}.\end{array}\right)}{\left(\begin{array}{c}\mathrm{median}\mathrm{FIR}\mathrm{in}0\%\mathrm{Inh}.-\\ \mathrm{median}\mathrm{FIR}\mathrm{in}100\%\mathrm{Inh}.\end{array}\right)}\right\}100& \left[\mathrm{Math}.1\right]\end{array}$

(372) This analysis is performed using a computerized specific program designed for FDSS generated data. Fluorescence ratio values are plotted using XLfit to determine an IC.sub.50 value for each compound.

(373) All tested compounds show less than about 3 microM of IC.sub.50 against Na.sub.v1.3 and/or Na.sub.v1.7 in the above assays. Preferable compounds show less than about 1 microM of IC.sub.50 against Na.sub.v1.3 and/or Na.sub.v1.7 in the above assays.

(374) Compounds with IC.sub.50 against Na.sub.v1.3<1 microM and/or Na.sub.v1.7<1 microM are:

(375) Examples 3, 12, 13, 14, 18, 20, 22, 23, 24, 25, 26, 29, 30, 31, 32, 37, 40, 42, 43, 46, 50, 54, 55, 56, 59, 60, 61, 64, 66, 67, 68, 75, 76, 78, 80, 84, 85, 89, 93, 94, 95, 102, 109, 110, 115, 118, 120, 122, 124, 125, 127, 128, 129, 132, 133, 136, 146, 147, 149, 150, 151, 152, 153, 154, 163, 167, 172, 174, 175, 176, 177, 179, 180, 181, 186, 187, 189, 190, 191, 192, 194, 195, 196, 197, 198, 199, 200, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216, 218, 219, 220, 221, 222, 223, 224, 226, 229, 230, 231, 232, 233, 234, 235, 236, 239, 241, 242, 243, 244, 245, 248, 250, 251, 252, 253, 255, 256, 260, 261, 262, 263, 264, 266, 269, 270, 274, 275, 276, 277, 278, 279, 282, 283, 284, 286, 287, 288, 289, 290, 291, 292, 293, 294, 295, 298, 299, 300, 301, 302, 303, 307, 309, 310, 311, 313, 315, 316, 317, 318, 319, 321, 322, 324, 325, 326, 327, 330, 331, 332, 335, 336, 337, 338, 339, 340, 341, 342, 343, 344, 345, 346, 347, 348, 349, 350, 351, 353, 354, 356, and 359.

(376) Regarding all tested compounds, the ratio of activities against Na.sub.v1.5 vs. Na.sub.v1.3 or Na.sub.v1.7 is more than three times. For example, the activities of Example 12 against Na.sub.v1.5, Na.sub.v1.3 and N.sub.v1.7 are more than 30 microM, 0.51 microM, and 1.0 microM, respectively.

(377) Electrophysiology Assay for Navs

(378) Whole cell patch clamp recording is used to assess the efficacy or selectivity of Na channel blocker on human Na.sub.v1.3 (hSCN3A) expressing HEK293 cells or human N.sub.v1.7 (hSCN9A) expressing CHO cells. Human Na.sub.v1.3 expressing HEK293 cells are grown in growth media which contain: Dulbecco's Phosphate-Buffered Saline (DMEM), 10% heat-inactivated fetal bovine serum (FBS) (Hyclone Laboratories Inc), 100 microgram/mL Penicillin/100 U/mL Streptomycin, 150 microgram/mL Zeocin, 3 microgram/mL Geneticin. Human Na.sub.v1.7 expressing CHO cells are grown in growth media which comprised: HAM/F-12, 9% heat-inactivated FBS (Hyclone Laboratories Inc) and 100 microgram/mL Penicillin/100 U/mL Streptomycin, 100 microgram/mL Hygromycin.

(379) Na channel expressing cells are dissociated by 0.05% trypsine-EDTA, and then seeded on cover glass for 24 to 48 hr.

(380) Glass pipettes are pulled to a tip diameter of 1 to 2 micrometer on a pipette puller. The pipettes are filled with the intracellular solution and a chloridized silver wire is inserted along its length, which is then connected to the headstage of the voltage-clamp amplifier (Axon Instruments or HEKA elektronik). The extracellular recording solution consists of (mM): 140 NaCl, 5 KCl, 2 CaCl.sub.2, 1 MgCl.sub.2, 10 HEPES, and 10 Glucose, pH 7.4 adjusted with NaOH. The internal solution consists of (mM): 120 CsF, 15 NaCl, 10 EGTA, 10 HEPES, pH 7.2 adjusted with CsOH; Upon insertion of the pipette tip into the bath, the pipette resistance is noted (acceptable range is between 1 to 3 megaohm). The junction potential between the pipette and bath solutions is zeroed on the amplifier. After establishing the whole-cell configuration, approximately 10 minutes are allowed for the pipette solution to equilibrate within the cell before beginning recording. Currents are lowpass filtered between 2 to 5 kHz and digitally sampled at 10 kHz.

(381) The normalized steady-state inactivation curve is constructed using 2 sec (for vehicle) or 60 sec (for drugs) conditioning pulse to different potentials followed immediately by the test pulse to 10 mV. Peak currents are plotted as fraction of the maximum current at the conditioning potentials ranging from 120 mV to 40 mV for Na.sub.v1.3 and from 130 mV to 60 mV for Na.sub.v1.7. V1/2 or k values are estimated from Boltzmann fits. The affinity of drugs to resting state of Na channels (K.sub.resting or K.sub.r) is assessed by 30 msec test pulse from a negative holding potential of 120 or 130 mV, where virtually all channels are in the resting state. K.sub.r value is calculated by a conventional 1:1 binding model:
K.sub.resting(K.sub.r)={[drug]I.sub.max,drug/(I.sub.max,controlI.sub.max,drug)}

(382) where K.sub.resting (=K.sub.r) is a dissociation constant for the resting state and [drug] is compound concentration. I.sub.max, control and I.sub.max, drug are peak currents in the absence and presence of compound, respectively.

(383) The affinity of drug to inactivated state of Na channels (K.sub.inact or K.sub.i) is estimated from the shift of the availability curve by compound. Interaction of the compound with the channel on inactivated state is evaluated by the following equation:
K.sub.inact(K.sub.i)={[drug]/((1+[drug]/Kr)*exp(V/k)1)}[Math.2]
where K.sub.inact (=K.sub.i) is a dissociation constant for the inactivated state. V is the compound-induced voltage shift of half maximal voltage of Boltzmann curve and k is the slop factor on presense of compound.

(384) All tested compounds of the invention show potent activities in this model. For example, the activities (Ki) of Example 29 against Na.sub.v1.7 is 0.95 microM.

(385) In Vivo Assay

(386) Chronic Constriction Injury (CCI)-Induced Static Allodynia in Rats

(387) Male Sprague-Dawley rats at 7 weeks old are purchased from Charles River Japan Inc., and housed in groups of two per cage under a 12-h light/dark cycle (lights on at 07:00) with access to food and water ad libitum. CCI-induced static allodynia is assessed by von Frey hair (VFH) test. Surgery is performed according to the method of Bennett G J and Xie Y K (Pain 1988, 33: 87-107). The animals are anesthetized with intraperitoneal injection of pentobarbital sodium. The left common sciatic nerve is exposed at the level of the middle of the thigh, freed of adhering tissue, and four ligatures are loosely tided around it by using 4-0 silk thread. The incision is sutured, and the rats are allowed to recover in their cages with soft bedding. Sham operation is performed in the same manner except of sciatic nerve ligation. The animals are individually placed in a Plexiglas test chamber on an elevated grid to acclimate for 1 hour before the day of testing. On postoperative day (POD) 14-28, evaluation is performed using a series of calibrated VFH (Semmes-Winstein monofilaments) with 0.4, 0.6, 1, 2, 4, 6, 8 and 15 g force. VFH starting with the 2 g force is applied in an ascending or descending fashion according to a modified Dixon up-down method described by Chaplan S R et al. (J Neurosci Methods 1994, 53: 55-63). Each VFH is presented to the plantar surface of the operated hind paw with steady upward pressure until bent for approximately 6 seconds. In the absence of a paw withdrawal, a stronger stimulus is presented. In the event of a paw withdrawal, the next weaker stimulus is chosen. After the initial change from positive to negative or vice verse, 4 more stimulations are applied. The 6-score pattern of positive and negative responses is converted into a 50% paw withdrawal threshold (PWT) using the following formula:
50% PWT(g)=(10.sup.[Xf+])/10,000[Math.3]
where Xf is the value (in log units) of the final VFH used, is the tabular value for the pattern of positive/negative responses and is the mean difference between stimuli in log units (here, 0.224).

(388) In the cases where continuous positive or negative responses are observed all the way out to the end of the stimulus spectrum, values of 0.25 and 15 g are assigned, respectively. The animals showing static allodynia (<3 g of 50% PWT) by CCI surgery are selected for evaluation and randomized to be nearly equal mean 50% PWT across all groups. The compounds of the invention or their vehicles are administered systemically. The rats are habituated to the chamber for at least 20 minutes before each measurement. The 50% PWT is measured at the appropriated time after compound administration.

(389) All tested compounds of the invention show potent activities in this model.

(390) Complete Freund's Adjuvant (CFA)-Induced Thermal Hyperalgesia in Rats

(391) Male Sprague-Dawley rats at 6 weeks old are purchased from Charles River Japan Inc., and housed in groups of two per cage under a 12-h light/dark cycle (lights on at 07:00) with access to food and water ad libitum. CFA-induced thermal hyperalgesia is assessed using the plantar test apparatus (Ugo Basile) as described by Hargreaves K et al. (Pain 1988, 32: 77-88). The animals are placed in an apparatus consisting of individual testing box on an elevated glass table and allowed to acclimate for at least 10 minutes. Following the habituation, a mobile radiant heat source is located under the table and heat stimulation is applied to the plantar surface of the right hind paw. The latency to remove its hind paw is defined as paw withdrawal latency (PWL) in sec. The cut-off point is set at 30 seconds to prevent tissue damage. CFA is prepared at a concentration of 2 to 3 mg/mL of Mycobacterium tuberculosis H37 RA in liquid paraffin. After disinfections with 70% ethanol, the rats are injected intraplantarly with 100 microL of CFA (200-300 microgram) into the right hind paw. Two days after CFA injection, PWL is measured in the same manner as mentioned above. The animals showing decrease of the PWL (hyperalgesia) by CFA injection are selected for evaluation and randomized to be nearly equal mean PWL across all groups. The compounds of the invention or their vehicles are administered systemically. The rats are habituated to the apparatus for at least 10 minutes before each measurement. The PWL is measured at the appropriated time after compound administration.

(392) All tested compounds of the invention show potent activities in this model.

(393) CFA-Induced Weight Bearing Deficit in Rats

(394) Male Sprague-Dawley rats at 7 weeks old are purchased from Charles River Japan Inc., and housed in groups of two per cage under a 12-h light/dark cycle (lights on at 07:00) with access to food and water ad libitum. CFA-induced weight bearing (WB) deficit is assessed using Incapacitance Tester (Linton Instrumentation). The animals are habituated to a plastic case that comes with Incapacitance tester before the day of CFA injection. On the day of CFA injection, the weight distribution of each hind paw is measured 3 times per rat using the tester, and the difference of weight distribution, weight on the right (injected) paw minus weight on left (non-injected) paw, is defined as WB deficit value in g. The duration of the each measurement is adjusted to 3 seconds. CFA is prepared at a concentration of 2-3 mg/mL of Mycobacterium tuberculosis H37 RA in liquid paraffin. After disinfections with 70% ethanol, the rats are injected intraplantarly with 100 microL of CFA (200-300 microgram) into the right hind paw. Two days after CFA injection, the weight distribution of each hind paw is measured and the WB deficit value is calculated in the same manner as mentioned above. The animals showing decrease of the WB deficit (>30%) by CFA injection are selected for evaluation and randomized to be nearly equal across all groups. The compounds of the invention or their vehicles are administered systemically. The weight distribution of each hind paw is measured at the appropriated time after compound administration, and the WB deficit value is calculated as previously explained.

(395) All tested compounds of the invention show potent activities in this model.

(396) Paw Incision-Induced Static Allodynia in Rats

(397) Male Sprague-Dawley rats at 7 weeks old are purchased from Charles River Japan Inc., and housed in groups of two per cage under a 12-h light/dark cycle (lights on at 07:00) with access to food and water ad libitum. Paw incision-induced static allodynia is assessed by VFH test. Surgery is performed according to the procedure described by Brennan et al. (Pain 1996, 64: 493-501). The animals are initially anesthetized with 3-4% isoflurane/O.sub.2 mixture in an anesthetic chamber and maintained with 2-3% delivered through a nose cone. The plantar surface of the right hind paw is sterilized with 7.5% povidone-iodine solution. A 1-cm longitudinal incision is made with a number 11 blade, through skin and fascia of the plantar aspect of the paw, starting 0.5 cm from the proximal edge of the heel and extending toward the toes. The plantaris muscle is elevated using forceps and retracted. The muscle origin and insertion remain intact. After hemostasis with gentle pressure, the skin is apposed with 2 sutures of 5-0 nylon. The wound site is covered with Terramycin ointment, and the rats are allowed to recover in their cages with soft bedding. The animals are individually placed in a Plexiglas test chamber on an elevated grid to acclimate for 1 hour before the day of surgery. On POD1, evaluation is performed using a series of calibrated VFH (0.008, 0.02, 0.04, 0.07, 0.16, 0.4, 0.6, 1, 1.4, 2, 4, 6, 8, 10, 15 and 26 g). Starting with the 0.16 g force in an ascending or descending fashion, each VFH is presented to the proximal end of the wound near the lateral heel with steady upward pressure until bent for approximately 6 seconds. In the absence of a paw withdrawal (negative response), a stronger stimulus is presented. In the event of a paw withdrawal (positive response), the next weaker stimulus is chosen. The lowest amount of force required to elicit two positive responses is defined as PWT in g. In the cases where continuous positive or negative responses are observed all the way out to the end of the stimulus spectrum, values of 0.008 and 26 g are assigned, respectively. The animals showing <1.4 g of PWT by incisional surgery are selected for evaluation and randomized to be nearly equal median PWT across all groups. The compounds of the invention or their vehicles are administered systemically. The rats are habituated to the chamber for at least 20 minutes before each measurement. The PWT is measured at the appropriated time after compound administration.

(398) All tested compounds of the invention show potent activities in this model.

(399) Paclitaxel-Induced Static Allodynia in Rats

(400) Male Sprague-Dawley rats at 7 weeks old are purchased from Charles River Japan Inc., and housed in groups of two per cage under a 12-h light/dark cycle (lights on at 07:00) with access to food and water ad libitum. Paclitaxel-induced static allodynia is assessed by VFH test. Treatment of paclitaxel is performed according to the method of Polomano R C et al. (Pain 2001, 94: 293-304). Paclitaxel (2 mg) is injected intraperitoneally on four alternate days (Days 1, 3, 5 and 7) in a volume of 1 mL/kg. Cumulative dose is 8 mg/kg. In sham group, the vehicle (a mixture of 16.7% Cremophor EL and 16.7% ethanol in saline) is treated as the same schedule. The animals are individually placed in a Plexiglas test chamber on an elevated grid to acclimate before the day of testing. On Days 15-29, evaluation is performed using a series of calibrated VFH with 0.4, 0.6, 1, 2, 4, 6, 8 and 15 g force. VFH starting with the 2 g force is applied in an ascending or descending fashion according to a modified Dixon up-down method described by Chaplan S R et al. (J Neurosci Methods 1994, 53: 55-63). Each VFH is presented to the plantar surface of the operated hind paw with steady upward pressure until bent for approximately 6 seconds. In the absence of a paw withdrawal, a stronger stimulus is presented. In the event of a paw withdrawal, the next weaker stimulus is chosen. After the initial change from positive to negative or vice versa, 4 more stimulations are applied. The 6-score pattern of positive and negative responses is converted into a 50% PWT using the following formula:
50% PWT(g)=(10.sup.[Xf+])/10,000
where Xf is the value (in log units) of the final VFH used, is the tabular value for the pattern of positive/negative responses and is the mean difference between stimuli in log units (here, 0.224).
In the cases where continuous positive or negative responses are observed all the way out to the end of the stimulus spectrum, values of 0.25 and 15 g are assigned, respectively. The animals showing static allodynia (<4 g of 50% PWT) by paclitaxel treatment are selected for evaluation and randomized to be nearly equal mean 50% PWT across all groups. The compounds of the invention or their vehicles are administered systemically. The rats are habituated to the chamber for at least 20 minutes before the measurement. The 50% PWT is measured at the appropriated time after compound administration. Statistical analysis is performed by unpaired t-test or ANOVA with Dunnett's post-hoc test compared to the vehicle group.
All tested compounds of the invention show potent activities in this model.

(401) Formalin-Induced Nociceptive Behaviors in Rats

(402) Male Sprague-Dawley rats at 6 weeks old are purchased from Charles River Japan Inc., and housed in groups of two per cage under a 12-h light/dark cycle (lights on at 07:00) with access to food and water ad libitum. Formalin test is performed during the light cycle. The animals are acclimated to the testing chamber for at least 30 minutes prior to formalin injection. A mirror is placed behind and/or under the chamber to aid observation. The 50 microL of 5% formalin solution is injected subcutaneously into the plantar surface of the right hind paw. Immediately after the injection, the rats are individually placed in the chamber, and the pain-related behaviors are recorded. After the testing, the time spent licking and/or biting of the injected paw are counted in 5-minutes bins for 45 minutes following the formalin treatment. The sum of time spent licking/biting in seconds from time 0 to 5 minutes is considered as the early phase, whereas the late phase is taken as the sum of time spent licking/biting typically from 15 to 45 minutes. The compounds of the invention or their vehicles are administered systemically at the appropriated time point before the formalin injection. Statistical analysis is performed by unpaired t-test or ANOVA with Dunnett's post-hoc test compared to the vehicle group.

(403) All tested compounds of the invention show potent activities in this model.

(404) Human Dofetilide Binding Assay

(405) Human HERG transfected HEK293S cells are prepared and grown in-house. The collected cells are suspended in 50 mM Tris-HCl (pH 7.4 at 4 C.) and homogenized using a handheld Polytron PT 1200 disrupter set at full power for 20 sec on ice. The homogenates are centrifuged at 48,000g at 4 C. for 20 min. The pellets are then resuspended, homogenized, and centrifuged once more in the same manner. The final pellets are resuspended in an appropriate volume of 50 mM Tris-HCl, 10 mM KCl, 1 mM MgCl.sub.2 (pH 7.4 at 4 C.), homogenized, ali-quoted and stored at 80 C. until use. An aliquot of membrane fractions is used for protein concentration determination using BCA protein assay kit (PIERCE) and ARVOsx plate reader (Wallac). Binding assays are conducted in a total volume of 30 microL in 384-well plates. The activity is measured by PHERAstar (BMG LABTECH) using fluorescence polarization technology. Ten microL of test compounds are incubated with 10 microL of fluorescence ligand (6 nM Cy3B tagged dofetilide derivative) and 10 microL of membrane homogenate (6 microgram protein) for 120 minutes at room temperature. Nonspecific binding is determined by 10 microM E4031 at the final concentration.

(406) All tested compounds of the invention show higher IC.sub.50 values in human dofetilide binding than IC.sub.50 values in Na.sub.v1.3 or Na.sub.v1.7 FRET Assay. The high IC.sub.50 values in human dofetilide binding activities lead to reducing the risk of cardiovascular adverse events.

(407) Metabolic Stability Assay:

(408) Half-Life in Human Liver Microsomes (HLM)

(409) Test compounds (1 microM) are incubated with 3.3 mM MgCl.sub.2 and 0.78 mg/mL HLM (HL101) or 0.74 mg/mL HLM (Gentest UltraPool 150) in 100 mM potassium phosphate buffer (pH 7.4) at 37 C. on the 96-deep well plate. The reaction mixture is split into two groups, a non-P450 and a P450 group. Nicotinamide adenine dinucleotide phosphate (NADPH) is only added to the reaction mixture of the P450 group. (NADPH generation system is also used instead of NADPH.) An aliquot of samples of P450 group is collected at 0, 10, 30, and 60 min time point, where 0 min time point indicated the time when NADPH is added into the reaction mixture of P450 group. An aliquot of samples of non-P450 group is collected at 10 and 65 min time point. Collected aliquots are extracted with acetonitrile solution containing an internal standard. The precipitated protein is spun down in centrifuge (2000 rpm, 15 min). The compound concentration in supernatant is measured by LC/MS/MS system.

(410) The half-life value is obtained by plotting the natural logarithm of the peak area ratio of compounds/internal standard versus time. The slope of the line of best fit through the points yield the rate of metabolism (k). This is converted to a half-life value using following equations: Half-life=ln 2/k

(411) The compounds of this invention show preferable stability, which show the above-mentioned practical use.

(412) Drug-Drug Interaction Assay

(413) This method essentially involves determining the percent inhibition of metabolites formation from probes (tacrine (Sigma A3773-1G) 2 microM, dextromethorphan (Sigma D-9684) 5 microM, diclofenac (Sigma D-6899-10G) 5 microM, and midazolam (ULTRAFINE UC-429) 2 microM) at 3 microM of the each compound.

(414) More specifically, the assay is carried out as follows. The compounds (60 microM, 10 microL) are pre-incubated in 170 microL of mixture including 0.1 mg protein/mL human liver microsomes, 100 mM potassium phosphate buffer (pH 7.4), 1 mM MgCl.sub.2 and probes as substrate for 5 min. Reaction is started by adding a 20 microL of 10 mM NADPH (20 microL of NADPH generating system, which consist of 10 mM NADP.sup.+, 50 mM DL-isocitric acid and 10 U/mL isocitric dehydrogenase, is also used). The assay plate is incubated at 37 C. Acetonitrile is added to the incubate solution at appropriate time (e.g. 8 min).

(415) The metabolites' concentration in the supernatant is measured by LC/MS/MS system.

(416) The degree of drug drug interaction is interpreted based on generation % of metabolites in the presence or absence of test compound.

(417) The compounds of this invention show preferable results, which show the above-mentioned practical use.

(418) Plasma Protein Binding Assay

(419) Plasma protein binding of the test compound (1 microM) is measured by the method of equilibrium dialysis using 96-well plate type equipment.

(420) HTD96a, regenerated cellulose membranes (molecular weight cut-off 12,000-14,000, 22 mm120 mm) are soaked for overnight in distilled water, then for 15 minutes in 30% ethanol, and finally for 20 minutes in dialysis buffer (Dulbecco's phosphate buffered saline, pH7.4). Frozen plasma of human, Sprague-Dawley rats, and Beagle dogs are used. The dialysis equipment is assembled and added 150 microL of compound-fortified plasma to one side of each well and 150 microL of dialysis buffer to the other side of each well. After 4 hours incubation at 37 C. for 150 rpm, aliquots of plasma and buffer are sampled. The compound in plasma and buffer are extracted with 300 microL of acetonitrile containing internal standard compounds for analysis. The concentration of the compound is determined with LC/MS/MS analysis.

(421) The fraction of the compound unbound is calculated by the following equation (A) or (B):
[Math.4]
fu=1{([plasma].sub.eq[buffer].sub.eq)/([plasma].sub.eq)}(A)
wherein [plasma].sub.eq and [buffer].sub.eq are the concentrations of the compound in plasma and buffer, respectively.

(422) $\begin{array}{cc}\left[\mathrm{Math}.5\right]& \\ \mathrm{fu}\left(\%\right)=\frac{\mathrm{Cb}/\mathrm{Cis},b4}{\mathrm{Cp}/\mathrm{Cis},p\frac{4}{3}}100& \left(B\right)\end{array}$
wherein Cp is the peak area of the compound in plasma sample;
Cis,p is the peak area of the internal standard in plasma sample;
Cb is the peak area of the compound in buffer sample;
Cis,b is the peak area of the internal standard in buffer sample;
4 and 4/3 is the reciprocal of the dilution rate in plasma and buffer, respectively.
The compounds of this invention show preferable plasma protein binding, which show the above-mentioned practical use.

(423) Equilibrium Aqueous Solubility Study

(424) The DMSO solution (2 microL, 30 mM) of each compound is dispensed into each well of a 96-well glass bottom plate. Potassium phosphate buffer solution (50 mM, 198 microL, pH 6.5) is added to each well, and the mixture is incubated at 37 C. with rotation shaking for 24 hours. After centrifugation at 2000 g for 5 minutes, the supernatant is filtered through the polycarbonate Isopore Membrane. The concentration of samples is determined by a general gradient HPLC method (J. Pharm. Sci., 2006, 95, 2115-2122).

(425) All publications, including but not limited to, issued patents, patent applications, and journal articles, cited in this application are each herein incorporated by reference in their entirety. Although the invention has been described above with reference to the disclosed embodiments, those skilled in the art will readily appreciate that the specific experiments detailed are only illustrative of the invention. It should be understood that various modifications can be made without departing from the spirit of the invention. Accordingly, the invention is limited only by the following claims.

INDUSTRIAL APPLICABILITY

(426) The amide derivatives of the present invention are useful in the treatment of a wide range of disorders, particularly pain, acute pain, chronic pain, neuropathic pain, inflammatory pain, visceral pain, nociceptive pain including post-surgical pain, and mixed pain types involving the viscera, gastrointestinal tract, cranial structures, musculoskeletal system, spine, urogenital system, cardiovascular system and CNS, including cancer pain, back pain, orofacial pain and chemo-induced pain.