FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to quinolone and acridine compounds of the formula (I) or their pharmaceutically acceptable salt where R2 - H, (C1-C6)-alkyl, (C1-C4)-fluoroalkyl; R3 - H, CN, (C1-C6)-alkyl, (C1-C6)-fluoroalkyl, ethanoyl; or R2 and R3 form 1,4-butanediyl; R4 means a group of the formula (II) ; - H; R8 - H, (C1-C4)-alkoxy, NO2, CN, (C1-C4)-fluoroalkyl, halogen, (C1-C4)-alkyl; R9 - H, halogen, (C1-C4)-alkyl or (C1-C4)-fluoroalkyl; or R8 and R9 taken together form (C1-C3)-alkylenedihydroxy-group; R10 and R11 - H, -alkyl. Invention proposes also a compound of the formula (III) which is subjected for decarboxylation or dehydration to obtain a compound (I) where R3 - H. Invention proposes other methods for synthesis of compounds (I) also. Pharmaceutical composition has compounds based on these compounds and it shows relaxing effect on bladder smooth muscles. EFFECT: improved methods of synthesis, enhanced effectiveness of compounds. 18 cl, 43 ex, 3 dwg
Title |
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