FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention relates to benzenesulfone derivatives of the formula (I) where R1 means hydrogen atom; R2 means hydrogen atom, trifluoromethyl group or (lower) alkyl; R3 means hydrogen atom or amino-group; or R1 and R2 or R3 and R2 in common form the group -CH=CH-CH=CH-; Z means pyrimidine-4-yl, pyridine-4-yl, pyridine-2-yl or phenyl; R4 and R5 each means independently hydrogen atom, (lower) alkyl, trifluoromethyl group, halogen atom, (lower) alkoxyl-group, nitrile, amino-group, (lower) alkylamino-group, di-(lower) alkylamino-group, piperazinyl, morpholinyl, pyrrolidinyl, vinyl, C3-C6-cycloalkyl, C3-C6-cycloalkenyl, tert. -butylethynyl, hydroxyalkylethynyl, phenylethynyl, naphthyl, thiophenyl or phenyl that can be substituted with halogen atom, (lower) alkoxyl-group, (lower) alkyl, trifluoromethyl group or nitro-group, or group , -morpholine-4-yl or ; n=2-4; R6 and R7 each means independently each of other hydrogen atom or (lower) alkyl, and their pharmaceutically acceptable salts. Invention describes also a medicinal agent based on the claimed compounds that elicit selective affinity to 5-HT-6 receptors. They are useful for treatment and prophylaxis of the central nervous system disturbances. EFFECT: valuable medicinal properties of compounds. 11 cl, 1 tbl
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Authors
Dates
2003-04-10—Published
1999-01-15—Filed