FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention relates to compounds of the formula (I): wherein: R1 represents hydrogen, halogen atom, CF3,, (1-3C)-alkyl or CN; m = 0, 1 or 2; R2 represents hydrogen atom or (1-3C)-alkyl; n = 3, 4, 5 or 6; R3 represents hydrogen, halogen atom or (1-4C)-alkyl; p = 0, 1 or 2, or its pharmacologically acceptable acid- -additive salt. Compounds by cl. 1 are prepared by interaction of compound of the formula (II): with compound of the formula (III): wherein L represents removable group, such as bromine atom. Compounds by cl. 1 can be prepared also by reduction of compound of the formula (IV): wherein A represents group -(CH2)n-1 to corresponding compound wherein A represents group -(CH2)n-1-NH2, and prepared amino- -derivative is subjected for interaction with derivative of phthalic anhydride of the formula (V): . Invention provides preparing 3-tetrahydropyridine-4-ylindoles eliciting high affinity to dopamine D2-receptor and inhibiting reuptake of serotonin. EFFECT: improved preparing method, valuable medicinal properties of compounds. 5 cl, 1 tbl
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Authors
Dates
2004-01-27—Published
1999-10-15—Filed