FIELD: organic chemistry, pharmacy. SUBSTANCE: invention proposes dimers of compounds 4-phenylpiperidine, 4-phenyl-1,2,3,6-tetrahydropyridine or 4-phenylpiperazine or dimers of spirocyclic piperidine of the general formula (I) where n has values from 1 to 5; R1-R4 mean hydrogen atom, halogen atom, trifluoromethyl-group, C1-6-alkyl; R5 and R6 each means hydrogen atom or bound they form ethylene bridge; X means O, S, SO2, CO or (CH2)m where m = 0 or 1, or X means NR7 where R7 means C1-6-alkyl, cycloalkyl, phenyl, or X means CR8R9 where R8 and R9 are taken from hydroxyl and phenyl optionally substituted with halogen atom and (1) Z1 means hydrogen atom and Z2 means (CH2)p where p = 0; Y means N, C or CH and dotted line indicates optional bond, i. e. if Y is C then it means a bond; (2) Z1 and Y are bound by a simple bond forming spirocyclic structure and in this case Y means C and dotted line indicates the absence of a bond; Z1 means O, S, (CH2)q where q = 1, 2 or 3; or Z1 means CH2O,CH2S,CH2CH2O,CH2CH2S, CH=CH, CH=CHCH2,CH2OCH2,CH2SCH2 and Z2 means O, S or (CH2)p where p = 0 or 1. Synthesized compounds can be used as ligands of sigma-receptors. Invention relates to a pharmaceutical composition binding sigma-receptors also. EFFECT: improved method of synthesis, sigma-receptor binding. 10 cl, 1 tbl, 14 ex
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Authors
Dates
1999-04-27—Published
1993-06-09—Filed