| abstract |
7-Substituted-6-fluor-1,4-dihydro-4-oxo-quinoline-, naphthyridine- and benzoxazine carboxylic acids of formula (I), wherein R<1> is a cycloalkyl group or a phenyl group which may be substituted by one or two halogen atoms; R<2> is hydrogen, a halogen atom, an alkyl group, a hydroxy group or an amino group; R<3> is hydrogen, hydroxy or amino; R<4> is a 1,2,3-triazol-1-yl group, a 1,2,4-triazol-1-yl group, a 1,2,3,4-tetrazol-1-yl or a 1,2,3,4-tetrazol-2-yl group, each of which may have 1 to 2 substituents selected from the group consisting of alkyl, COOH, CH2NH2, amino and phenyl groups; and x is N, CH, C-F or C-OCH3; n is 0, 1 or 2; or (II) may be (III), are described, as well as a process for their preparation and their use as antibacterial agents. |