FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to derivatives of 5-phenyl-3-(piperidine-4-yl)-1,3,4-oxadiazole- -2(3H)-one of the general formula (I) where R1 means the group (C1-C4)-alkyl or (C3-C7)-cycloalkylmethyl; X1 means hydrogen or halogen atom or (C1-C4)-alkoxy-group or OR1 and X1 in common mean the group of the formula -OCH2O-, -O(CH2)2-, -O(CH2)2O- or -O(CH2)3O-; X2 means hydrogen atom or amino-group; X3 means hydrogen or halogen atom and R2 means hydrogen atom or possibly substituted group (C1-C6)-alkyl, or the group phenyl-(C1C4)-alkyl that can be substituted with phenyl ring, or the group phenyl-(C2-C3)-alkenyl, or the group phenoxy-(C2C4)-alkyl, or the group cyclo-(C3-C7)-alkylmethyl, or the group 2,3-dihydro-1H-indene-1-yl, or the group 2,3-dihydro-1H- -indene-2-yl, or the group of the general formula -(CH2)n-CO-Z where n = 1-6 and Z means the group piperidine-1-yl or 4-(dimethylamino)-piperidine-1-yl. Indicated compounds can be used for treatment and prophylaxis of disorders with implication of receptors 5-HT4 and/or H3, especially in the central nervous system, gastroenteric tract, lower urogenital organs or cardiovascular system. Invention describes method of synthesis of indicated compounds, pharmaceutical composition and drug also. EFFECT: improved method of synthesis, valuable medicinal and pharmacological properties. 7 cl, 1 tbl, 18 ex
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