Compounds with a combination of cannabinoid CB
Compounds with a combination of cannabinoid CB 1 antagonism and serotonin reuptake inhibition, pharmaceutical compositions containing these compounds, methods for preparing these compounds, methods for preparing novel intermediates useful for their synthesis, and methods for preparing these compositions are disclosed. Uses of such compounds and compositions, particularly their use in administering them to patients to achieve a therapeutic effect in psychosis, anxiety, depression, attention deficits, cognitive disorders, obesity, drug dependence, Parkinson's disease, Alzheimer's disease, pain disorders, neuropathic pain disorders and sexual disorders are disclosed. In at least one embodiment, the invention relates to compounds of the general formula (1): wherein the substitutents have the definitions given in the specification.
1. A compound of formula (1):
or a tautomer, stereoisomer, N-oxide, or a pharmacologically acceptable salt of any of the foregoing, wherein:
A is (A 2 ):
wherein the wavy bond is the point at which the fragment is attached to moiety N (wherein N represents a non-basic nitrogen atom) in formula (1), R 1 and R 2 independently are chosen from a hydrogen atom, a trifluoromethyl group, and a halogen atom, R 4 is chosen from a hydrogen atom, a halogen atom, methyl, ethyl, trifluoromethyl, hydroxymethyl, fluoromethyl, 2,2,2-trifluoroethyl, propyl, methylsulfanyl, methylsulfinyl, methylsulfonyl, ethylsulfanyl, ethylsulfinyl, ethylsulfonyl, C 1 3 -dialkyl-aminomethyl, pyrrolidin-1-ylmethyl, piperidin-1-ylmethyl, and morpholin-4-ylmethyl group, and
the NRTB sequence of formula (1) is chosen from one of the fragments (NRTB 1 ), (NRTB 2 ), (NRTB 3 ), (NRTB 5 ), (NRTB 6 ), (NRTB 7 ), (NRTB 8 ), (NRTB 9 ), and (NRTB 10 ):
wherein R is chosen from a hydrogen atom and a (C 1 -C 3 )-alkyl group.
2. A compound as claimed in claim 1 , wherein A is:
wherein the wavy bond is the point at which the fragment is attached to the non-basic nitrogen atom N in formula (1).
3. A compound chosen from:
2-(2-chlorophenyl)-1-(4-chlorophenyl)-5-ethyl-1H-imidazole-4-carboxylic acid [7-(2-amino-ethoxyimino)-7[4-(trifluoromethyl)phenyl] heptyl]amide; and
[2-(2-chlorophenyl)-1-(4-chlorophenyl)-5-ethyl-1H-imidazole-4-yl] {4-[4-(5-fluoro-1H-indol3-yl)butyl]piperazin-1-yl}methanone.
4. A compound as claimed in claim 1 , wherein said compound is an optically active enantiomer.
5. A pharmaceutical composition comprising, at least one pharmaceutically acceptable carrier and/or at least one pharmaceutically acceptable auxiliary substance, a pharmacologically active amount of at least one compound of formula (1):
or a tautomer, stereoisomer, N-oxide, or a pharmacologically acceptable salt of any of the foregoing, wherein:
A is (A 2 ):
wherein the wavy bond is the point at which the fragment is attached to moiety N (wherein N represents a non-basic nitrogen atom) in formula (1), R 1 and R 2 independently are chosen from a hydrogen atom, a trifluoromethyl group, and a halogen atom, R 4 is chosen from a hydrogen atom, a halogen atom, methyl, ethyl, trifluoromethyl, hydroxymethyl, fluoromethyl, 2,2,2-trifluoroethyl, propyl, methylsulfanyl, methylsulfinyl, methylsulfonyl, ethylsulfanyl, ethylsulfinyl, ethylsulfonyl, C 1-3 -dialkyl -aminomethyl, pyrrolidin-1-ylmethyl, piperidin-1-ylmethyl, and morpholin-4-ylmethyl group, and
the NRTB sequence of formula (1) is chosen from one of the fragments (NRTB 1 ), (NRTB 2 ), (NRTB 3 ), (NRTB 5 ), (NRTB 6 ), (NRTB 7 ), (NRTB 8 ), (NRTB 9 ), and (NRTB 10 ):
wherein R is chosen from a hydrogen atom and a (C 1 -C 3 )-alkyl group.