2,5-disubstituted phenyl carboxamide orexin receptor antagonists
The present invention is directed to 2,5-disubstituted phenyl carboxamide compounds which are antagonists of orexin receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which orexin receptors are involved.
1. A compound of the formula I:
wherein:
A 1 is selected from the group consisting of phenyl and pyridyl;
A 2 is selected from the group consisting of phenyl and pyridyl;
A 3 is selected from the group consisting of phenyl, naphthyl, C 3-6 cycloalkyl, and heterocycle;
R 1a , R 1b and R 1c may be absent if the valency of A 1 does not permit such substitution and are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxyl,
(4) C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl, phenyl or napthyl,
(5) —O—C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl,
(6) heteroaryl, wherein heteroaryl is selected from pyrrolyl, imidazolyl, indolyl, pyridyl, and pyrimidinyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ,
(7) phenyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ,
(8) —O-phenyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 , and
(9) —NH—C 1-6 alkyl, or —N(C 1-6 alkyl)(C 1-6 alkyl), which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ;
R 2a , R 2b and R 2c may be absent if the valency of A 2 does not permit such substitution and are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxyl,
(4) C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl or napthyl,
(5) —O—C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl,
(6) heteroaryl, wherein heteroaryl is selected from pyrrolyl, imidazolyl, indolyl, pyridyl, and pyrimidinyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ,
(7) phenyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ,
(8) —O-phenyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 , and
(9) —NH—C 1-6 alkyl, or —N(C 1-6 alkyl)(C 1-6 alkyl), which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ;
R 3a , R 3b and R 3c may be absent if the valency of A 3 does not permit such substitution and are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxyl,
(4) C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl, phenyl or napthyl,
(5) —O—C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl,
(6) heteroaryl, wherein heteroaryl is selected from pyrrolyl, imidazolyl, indolyl, pyridyl, and pyrimidinyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ,
(7) phenyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl, or NO 2 ,
(8) —O-phenyl, which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 , and
(9) —NH—C 1-6 alkyl, or —N(C 1-6 alkyl)(C 1-6 alkyl), which is unsubstituted or substituted with halogen, hydroxyl, C 1-6 alkyl, —O—C 1-6 alkyl or —NO 2 ;
R 4 is hydrogen and R 5 is hydrogen;
R 6 is hydrogen, C 1-6 alkyl or C 3-6 cycloalkyl;
or a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 wherein A 1 is phenyl.
3. The compound of claim 1 wherein A 1 is pyridyl.
4. The compound of claim 1 wherein A 2 is phenyl.
5. The compound of claim 1 wherein A 2 is pyridyl.
6. The compound of claim 1 wherein A 3 is phenyl.
7. The compound of claim 1 wherein R 1a , R 1b and R 1c are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen,
(3) hydroxyl,
(4) C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl or napthyl, and
(5) —O—C 1-6 alkyl, which is unsubstituted or substituted with halogen, hydroxyl or phenyl.
8. The compound of claim 7 wherein R 1a , R 1b and R 1c are independently selected from the group consisting of:
(1) hydrogen,
(2) chloro,
(3) fluororo, and
(4) methyl.
9. The compound of claim 1 wherein R 2a , R 2b and R 2c are independently selected from the group consisting of:
(1) hydrogen,
(2) chloro,
(3) fluoro,
(4) bromo,
(5) methoxy,
(6) t-butoxy,
(7) difluoromethyl, and
(8) trifluoromethyl.
10. The compound of claim 1 wherein R 3a , R 3b and R 3c are independently selected from the group consisting of:
(1) hydrogen,
(2) halogen, and
(3) C 1-6 alkyl.
11. A compound which is selected from the group consisting of:
N-(3,4-Dimethoxybenzyl)-3′,5′-dimethyl-4-pyridin-3-ylbiphenyl-3-carboxamide;
N-[(5,6-dimethoxypyridin-2-yl)methyl]-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(3-chloro-4-methoxybenzyl)-2-pyrazin-2-yl-5-(5-methylpyridin-3-yl)benzamide;
N-(3,4-dimethoxybenzyl)-3′,5′-dimethyl-4-(1-methyl-1H-pyrazol-4-yl)biphenyl-3-carboxamide;
3′,5′-dichloro-N-(3,4-dimethoxybenzyl)-4-pyridin-3-ylbiphenyl-3-carboxamide;
N-(3-chloro-4-methoxybenzyl)-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(3,4-dimethoxybenzyl)-2-(5-fluoropyridin-3-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(3-ethyl-4-methoxybenzyl)-3′,5′-dimethyl-4-pyrazin-2-ylbiphenyl-3-carboxamide;
N-[4-methoxy-3-(trifluoromethyl)benzyl]-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(4-ethyl-3-methoxybenzyl)-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-[4-(difluoromethoxy)-3-methoxybenzyl]-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(3-cyclopropyl-4-methoxybenzyl)-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(3,4-dimethoxybenzyl)-2-(4-methyl-1,3-oxazol-5-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-[(5,6-dimethoxypyridin-2-yl)methyl]-4-(5-methylpyridin-3-yl)biphenyl-2-carboxamide;
N-[(6-ethyl-5-methoxypyridin-2-yl)methyl]-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-[3,4-bis(difluoromethoxy)benzyl]-2-(1-methyl-1H-pyrazol-4-yl)-5-(5-methylpyridin-3-yl)benzamide;
N-(3-cyclopropyl-4-methoxybenzyl)-4-(5-fluoropyridin-3-yl)-3′,5′-dimethylbiphenyl-3-carboxamide;
N-(3-ethoxy-4-methoxybenzyl)-4-(5-fluoropyridin-3-yl)-3′,5′-dimethylbiphenyl-3-carboxamide;
N-[(6-cyclopropyl-5-methoxypyridin-2-yl)methyl]-4-(5-fluoropyridin-3-yl)-3′,5′-dimethylbiphenyl-3-carboxamide;
or a pharmaceutically acceptable salt thereof.
12. A pharmaceutical composition which comprises an inert carrier and a compound of claim 1 or a pharmaceutically acceptable salt thereof.
13. A method for enhancing the quality of sleep in a mammalian patient in need thereof which comprises administering to the patient a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof.
14. A method for treating insomnia in a mammalian patient in need thereof which comprises administering to the patient a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof.
15. A method for treating or controlling obesity in a mammalian patient in need thereof which comprises administering to the patient a therapeutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof.