FIELD: organic chemistry, medicine, pharmacy. SUBSTANCE: invention relates to new derivatives of 3(2)-pyridazinone of the general formula (I) where R1 - hydrogen atom, phenyl, methyl substituted with CH3O or CH3SO2NH, C2-C4-alkyl substituted with R8R9N, C3-C5-alkenyl substituted with phenyl optionally substituted with halogen atom; one of A and B is hydrogen atom and another - a group of the formula (II) where R2 and R3 - hydrogen atom independently, C1-C4-alkyl or they form piperazine or homopiperazine ring with adjacent group -N(CH2)nN-; R4 - hydrogen atom or C1-C4-alkyl; R5,R6 and R7 - hydrogen atom, C1-C4-alkoxy-group, CH3SO2NH; X - a simple valent bond, oxygen atom or a group -CH=CH-; m = 0-1; n = 2-3; R8 and R9 are C1-C4-alkyl independently or with nitrogen atom to which they are bond form morpholino- or 4-R10-piperazino-group where R10 is C1-C4-alkyl substituted with phenoxy-group or C3-C5-alkenyl substituted with phenyl-group or their acid-additive salts showing antiarrhythmic activity. Invention relates to also a pharmaceutical composition containing an effective amount of indicated compound in mixture with pharmaceutically acceptable carriers, diluting agents and/or filling agents. Invention proposes a method of an antiarrhythmic treatment that involves a prescription to patient an effective amount of indicated compound or its pharmaceutically acceptable salt. Activity of proposed compounds exceeds that of the known preparation, for example, sotalol. EFFECT: improved method of synthesis and treatment, enhanced activity of compounds synthesized. 6 cl, 4 tbl, 1 dwg
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Authors
Dates
1999-05-10—Published
1992-12-18—Filed