Xin T, Ding J, Zhang X P
Shanghai Institute of Pharmaceutical Industry.
Yao Xue Xue Bao. 1993;28(11):865-9.
The title compounds 6-24 were obtained by the reaction of 5 with corresponding benzaldehydes. 5 was prepared with ethyl 7-chloro-6-fluoro-1,4-dihydro-4-oxo-3- quinolinecarboxylate by hydrolysis, amination and condensation with piperazine. Anti-bacterial activities of 5-24 were tested in vitro.
标题化合物6 - 24是通过5与相应的苯甲醛反应得到的。5是由7 - 氯 - 6 - 氟 - 1,4 - 二氢 - 4 - 氧代 - 3 - 喹啉羧酸乙酯经水解、胺化并与哌嗪缩合制备而成。对5 - 24的抗菌活性进行了体外测试。