FIELD: medicine. SUBSTANCE: present invention describes quinolone-and napthyridonecarboxylic acid derivatives of formula I: wherein A is CH, CF, CCL, C-OCH3, C-CH3 and N′,; X1 is hydrogen, halogen, NH2, and CH3; R1 is alkyl having 1-3 carbon atoms, FCH2CH2-, cyclopropyl, phenyl which is mono-to trisubstituted by halogen: or A and R1 are C-O-CH2-CH(CH)3 bridge; R2 is hydrogen, alkyl having 1-3 carbon atoms which is substituted by hydroxy group, halogen or amino group, or 5-methyl-2-oxo-1,3-dioxol-4-yl-methyl; 8 is residue of formulae; wherein Y is 0 or CH2; R3 is oxoalkyl having 2-5 carbon atoms; CH2-CO-C6H5, CH2CH2CO2R′, , CH=CH-CO2R′ or CH2CH2-CN wherein R′ is hydrogen or alkyl having 1-3 carbon atoms, R4 is hydrogen, alkyl having 1-3 carbon atoms, oxoalkyl having 2-5 carbon atoms, CH2-CO-C6H5, CH2CH2CO2R′, R′O2C-CH=C-CO2R′, or CH2CH2-CN or 5-methyl-2-oxo-1,3-dioxol-4-yl methyl wherein R′ is hydrogen or alkyl having 1-3 carbon atoms, in admixture with isomers or individual isomers, hydrates and salts thereof. The present invention also describes method of preparation of drug containing said compounds. EFFECT: improved properties of the drug. 5 cl, 1 dwg, 4 tbl
Title |
Year |
Author |
Number |
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