Substituted N-phenyl-bipyrrolidine carboxamides and therapeutic use thereof
View Patent ↗The present invention discloses and claims a series of substituted N-phenyl-bipyrrolidine carboxamides of formula (I). wherein R, R 1 , R 2 , R 3 and R 4 are as described herein. More specifically, the compounds of this invention are modulators of H3 receptors and are, therefore, useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of diseases modulated by H3 receptors including diseases associated with the central nervous system. Additionally, this invention also discloses methods of preparation of substituted N-phenyl-bipyrrolidine carboxamides and intermediates therefor.
1. A method of therapeutically treating a disease in a patient, said disease selected from the group consisting of dementia, Alzheimer's disease, multiple sclerosis, schizophrenia, and attention deficit hyperactivity disorder, comprising administering to said patient a therapeutically effective amount of a compound of formula (I):
wherein
R, R 1 , R 2 and R 3 are the same or different and independently of each other chosen from hydrogen, (C 1 -C 4 )alkyl or CF 3 ;
R 4 is selected from the group consisting of cyclopropyl, cyclopentyl, cyclohexyl, bicyclo[2,2,1]heptyl, cyclopentylmethyl, tetrahydropyranyl, furanyl, 2-, 4- or 5-oxazolyl, 3-, 4- or 5-isoxazolyl and 3-, 4- or 5-pyrazolyl; wherein said R 4 is optionally substituted one or more times with a substituent selected from halogen, methyl, ethyl, pyridinyl, 2-oxo-2H-pyridin-1-yl and CF 3 ; or
a pharmaceutically acceptable salt thereof or an enantiomer or a diastereomer thereof optionally in combination with one or more pharmaceutically acceptable excipient, diluent or a carrier.
2. The method according to claim 1 , wherein the disease is schizophrenia.
3. The method according to claim 1 , wherein the disease is Alzheimer's disease.
4. The method according to claim 1 , wherein the disease is dementia.
5. The method according to claim 1 , wherein the compound is selected from the group consisting of:
cyclopropanecarboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
cyclopropanecarboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-2-trifluoromethyl-phenyl]-amide;
cyclopropanecarboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
cyclopropanecarboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2,2,3,3-tetramethyl-cyclopropanecarboxylic acid [2-methyl-4-(2(S)-methyl-[1,3′(S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2,2,3,3-tetramethyl-cyclopropanecarboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2,2,3,3-tetramethyl-cyclopropanecarboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2,2,3,3-tetramethyl-cyclopropanecarboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
cyclopentanecarboxylic acid [2-methyl-4-(2(S)-methyl-[1,3′(S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
cyclohexanecarboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2-cyclopentyl-N-[2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-acetamide;
2-cyclopentyl-N-[2-methyl-4-(2(S)methyl-[1,3′(S)]bipyrrolidinyl-1′-yl)-phenyl]-acetamide;
2-cyclopentyl-N-[4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-acetamide;
2-cyclopentyl-N-[3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-acetamide;
bicyclo[2.2.1]heptane-2-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
(1S,4R)-bicyclo[2.2.1]heptane-2-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
(1S,4R)-bicyclo[2.2.1]heptane-2-carboxylic acid [3-methyl-4-(2-methyl-[1,3]bipyrrolidinyl-1′-yl)-phenyl]-amide;
(1S,4R)-bicyclo[2.2.1]heptane-2-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
furan-3-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
furan-2-carboxylic acid [2-methyl-4-(2(S)-methyl-[1,3′(S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
5-(2-oxo-2H-pyridin-1-yl)-furan-2-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2-methyl-oxazole-4-carboxylic acid [2-methyl-4-(2(S)-methyl-[1,3′(S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3-methyl-isoxazole-5-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3,5-dimethyl-isoxazole-4-carboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3,5-dimethyl-isoxazole-4-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
1H-pyrazole-4-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
1H-pyrazole-4-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
1H-pyrazole-4-carboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
5-methyl-1H-pyrazole-3-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
5-methyl-1H-pyrazole-3-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
5-methyl-1H-pyrazole-3-carboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
5-methyl-1H-pyrazole-3-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
5-methyl-1H-pyrazole-3-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-2-trifluoromethyl-phenyl]-amide;
1,5-dimethyl-1H-pyrazole-3-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide; and
5-pyridin-4-yl-2H-pyrazole-3-carboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
or a pharmaceutically acceptable salt thereof.
6. The method according to claim 1 , wherein the compound is selected from the group consisting of:
cyclopropanecarboxylic acid [2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
2-cyclopentyl-N-[2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-acetamide;
cyclohexanecarboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
bicyclo[2.2.1]heptane-2-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
furan-3-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3-methyl-isoxazole-5-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide; and
3,5-dimethyl-isoxazole-4-carboxylic acid [3-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenyl]-amide;
or a pharmaceutically acceptable salt thereof.
7. The method according to claim 1 , wherein the compound is selected from the group consisting of:
cyclohexanecarboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
bicyclo[2.2.1]heptane-2-carboxylic acid [2-methyl-4-(2S-methyl-[1,3′S]bipyrrolidinyl-1′-yl)-phenyl]-amide;
tetrahydro-pyran-4-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide; and
3,5-dimethyl-isoxazole-4-carboxylic acid [2-methyl-4-(2(2S)-methyl-[1,3′(3′S)]bipyrrolidinyl-1′-yl)-phenyl]-amide;
or a pharmaceutically acceptable salt thereof.
8. The method according to claim 1 , wherein the compound is having the formula (II):
wherein R, R 1 , R 2 , R 3 and R 4 are as defined in claim 1 .