FIELD: organic synthesis. SUBSTANCE: invention provides quinolone- and naphthiridonecarboxylic acid derivatives of general formula T-Q, wherein Q is residue of general formula (a), in which R1 is C1-4-alkyl optionally substituted by 1-2 halogen atoms, cyclopropyl, or dihalogen substituted phenyl; R2 hydroxyl, C1-3-alkoxy; X1 halogen; X2 hydrogen, halogen, methyl, methoxy, amino, or vinyl; A nitrogen or CR3 group; R3 hydrogen, halogen, methyl, methoxy, vinyl, difluoromethoxy, or, together with R1 residue, -*O-CH2-CH-CH3 bridge, in which labeled oxygen atom is bound to A group carbon atom; and T is residue of general formula (b), wherein B is amino group and R4 hydrogen; isomer mixture or individual isomers in the form of hydrate or salt. Compounds T-Q show antibacterial activity. EFFECT: extended choice of antibacterial drugs. 4 cl, 2 tbl, 31 ex
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Authors
Dates
2000-02-20—Published
1995-10-03—Filed