Stefancich G, Artico M, Corelli F, Massa S, Panico S, Simonetti N
Farmaco Sci. 1985 Apr;40(4):237-48.
The synthesis of 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1H-pyrrol-1-yl)quinoline-3-carboxy lic acid, a new fluorinated high broad-spectrum antibacterial agent related to nalidixic acid is described. The title compound has been prepared by the reaction of 4-fluoro-3-(1H-pyrrol-1-yl)aniline with diethyl ethoxymethylenemalonate, cyclization of the malonate obtained to the quinolinecarboxylate ester, ethylation of the ester, followed by hydrolysis with aqueous sodium hydroxide. The new derivative proved very active against both gram-positive and gram-negative bacteria. Its activities in comparison with those of nalidixic acid, pipemidic acid, piromidic acid and enoxacin were found to be greatly superior with regard to the unfluorinated compounds and somewhat superior also to enoxacin. The known 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(pyrrolidin-1-yl)quinoline-3- carboxylic acid, here prepared by catalytic hydrogenation of the pyrrole moiety of the title compound, has been found to be less active as an antibacterial agent.
描述了一种与萘啶酸相关的新型含氟高广谱抗菌剂1-乙基-6-氟-1,4-二氢-4-氧代-7-(1H-吡咯-1-基)喹啉-3-羧酸的合成。标题化合物是通过4-氟-3-(1H-吡咯-1-基)苯胺与乙氧基甲基丙二酸二乙酯反应,将所得丙二酸环化生成喹啉羧酸酯,酯进行乙基化,然后用氢氧化钠水溶液水解制备的。新衍生物对革兰氏阳性菌和革兰氏阴性菌均表现出很高的活性。与萘啶酸、吡哌酸、匹美酸和依诺沙星相比,就未氟化的化合物而言,其活性大大优于它们,对依诺沙星也略占优势。通过标题化合物吡咯部分的催化氢化制备的已知1-乙基-6-氟-1,4-二氢-4-氧代-7-(吡咯烷-1-基)喹啉-3-羧酸,已发现其作为抗菌剂的活性较低。