Benzimidazole derivatives and their use for modulating the GABA
This invention relates to novel benzimidazole derivatives, pharmaceutical compositions containing these compounds, and methods of treatment therewith. The compounds of the invention are useful in the treatment of central nervous system diseases and disorders, which are responsive to modulation of the GABA A receptor complex, and in particular for combating anxiety and related diseases.
1. A compound of the general formula (I):
or an N-oxide thereof, or any of its stereoisomers or any mixture of its stereoisomers,
or a pharmaceutically acceptable salt thereof,
wherein R a , R b and R c independent of each other represent hydrogen, alkyl, cycloalkyl, cycloalkylakyl, alkenyl, alkynyl, hydroxy, alkoxy, alkoxyalkyl, arylalkyl, formyl, alkylcarbonyl or alkoxyalkylcarbonyl;
R d represents a heteroaryl group;
which heteroaryl group is optionally substituted with one or more substituents independently selected from the group consisting of:
halo, hydroxy, R′R″N—, R′R″N-alkyl, cyano, nitro, trifluoromethyl, trifluoromethoxy, hydrazino, alkoxy, cycloalkoxy, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, and alkynyl;
wherein R′ and R″ independent of each other are hydrogen or alkyl.
2. The compound of claim 1 , or an N-oxide thereof, or any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, wherein R a represents hydrogen, alkyl or arylalkyl.
3. The compound of claim 1 , or an N-oxide thereof, or any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, wherein R b represents hydrogen, alkyl, alkoxy, arylalkyl, formyl or alkylcarbonyl.
4. The compound of claim 1 , or an N-oxide thereof, or any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, wherein R c represents hydrogen or alkyl.
5. The compound of claim 1 , or an N-oxide thereof, or any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, wherein R d represents a heteroaryl group selected from thiazolyl, pyridyl, pyrimidyl and pyrazinyl;
which heteroaryl group is optionally substituted with one or more substituents independently selected from the group consisting of:
halo, hydrazino and alkoxy.
6. The compound of claim 1 , which is
C-[1-(3-Thiazol-2-yl-phenyl)-1H-benzoimidazol-5yl]-methylamine;
C-[1-(3-Pyridin-3-yl-phenyl)-1H-benzoimidazol-5-yl]-methylamine;
C-[1-(3-[6-Fluoro-pyridin-3-yl]-phenyl)-1H-benzoimidazol-5-yl]-methylamine;
C-[1-(3-[Pyridin-2-yl]-phenyl)-1H-benzoimidazol-5-yl]-methylamine;
C-[1-(3-Pyrazin-2-yl-phenyl)-1H-benzoimidazol-5-yl]methylamine;
1-[1-(3-Pyrazin-2-yl-phenyl)-1H-benzoimidazol-5-yl]-ethylamine;
1-[1-(3-Pyridin-3-yl-phenyl)-1H-benzoimidazol-5-yl]-ethylamine;
1-{1-[3-(6-Fluoro-pyridin-3-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethylamine;
1-{1-[3-(6-Hydrazino-pyridin-3-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethylamine;
1-[1-(3-Pyrimidin-5-yl-phenyl)-1H-benzoimidazol-5-yl]ethylamine;
N-[1-(3-Thiazol-2-yl-pheny)-1H-benzoimidazol-5-ylmethyl]-acetamide;
N-[1-(3-Pyridin-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]-acetamide;
N-(1-{1-[3-(2-Fluoro-pyridin-3-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethyl)-formamide;
N-(1-{1-[3-(2-Methoxy-pyridin-3-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethyl)-formamide;
N-(1-{1-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethyl)-formamide;
1-{1-[3-(2,4-Dimethoxy-pyrimidin-5-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethylamine;
1-{1-[3-(2-Methoxy-pyridin-3-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethylamine;
1-{1-[3-(2-Fluoro-pyridin-3-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethylamine;
Methyl-[1-(3-pyridin-3-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]-amine;
Dimethyl-[1-(3-pyridin-3-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]-amine;
Benzyl-{1- [1-(3-pyridin-3-yl-phenyl)-1H-benzoimidazol-5-yl]-ethyl}-amine;
Dibenzyl-{1-[1-(3-pyridin-3-yl-phenyl)-1H-benzoimidazol-5-yl]ethyl}-amine;
Methyl-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]amine;
Dimethyl-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]-amine;
Ethyl-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]amine;
Diethyl- [1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]-amine;
Benzyl-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]-amine;
Dibenzy-[1-(3-thiazol-2-yl-phenyl)-1H-benzoimidazol-5-ylmethyl]amine;
O-Methyl-N-{1-[1-(3-pyridin-3-yl-phenyl)-1H-benzoimidazol-5-yl]-ethyl}-hydroxylamine;
N-{1-[3-(thiazol-2-yl)-phenyl]-1H-benzoimidazol-5-ylmethyl}-formamide;
1-{1-[3-(5-Chloro-thiazol-2-yl)-phenyl]-1H-benzoimidazol-5-yl}-ethylamine;
or an N-oxide thereof, any of its isomers or any mixture of its isomers,
or a pharmaceutically acceptable salt thereof.
7. A pharmaceutical composition, comprising a therapeutically effective amount of a compound of claim 1 , or an N-oxide thereof, any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, together with at least one pharmaceutically acceptable carrier, excipient or diluent.
8. The compound of claim 1 , which is 1-{1-[3-(2-Methoxy-pyridin-3-yl)-phenyl]-1 H-benzoimidazol-5-yl}-ethylamine, or an N-oxide thereof, any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof.