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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL ACTIVITY OF SOME N-SUBSTITUTED DERIVATIVES OF 6-FLUORO-1-METHYL-4-OXO-7-(PIPERAZIN-1-YL)-4H-[1,3]THIAZETO[3,2-A]QUINOLINE-3-CARBOXYLIC ACID
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SYNTHESIS, CHARACTERIZATION AND ANTIBACTERIAL ACTIVITY OF SOME N-SUBSTITUTED DERIVATIVES OF 6-FLUORO-1-METHYL-4-OXO-7-(PIPERAZIN-1-YL)-4H-[1,3]THIAZETO[3,2-A]QUINOLINE-3-CARBOXYLIC ACID

机译:6-氟-1-甲基-4-甲基-4-氧代-7-(哌嗪-1-基)-4H- [1,3]噻吩并[3,2-A]的一些N-取代衍生物的合成,表征和抗菌活性QUINOLINE-3-羧酸

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Objective: N-substituted derivatives of 6-fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-4H-[1, 3] thiazeto [3, 2-a] quinoline-3-carboxylic acid: Synthesis and antibacterial activity. Me thods: In the present study N-substituted derivatives of 6-fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid were prepared by using Triethylamine and DMF. This procedure was modified by adding tetra butyl ammonium bromide (TBAB) to facilitate completion in few reactions. Other reactions which did not proceed in both the aforementioned ways were facilitated by the use of Morwet-D425. All the new title compounds were characterized by their spectral data and were screened for antibacterial activity. Results: Some of the reported compounds were synthesized using the process disclosed by us in U.S.Pat.No.8, 410,268B2. In our present work, we have achieved good yields and purity. Many compounds exhibited substantial antibacterial activity. Conclusion: It can be inferred that the title compounds with substituted phenyl and quinoline rings exhibited comparable antibacterial activity with respect to the standard
机译:目的:6-氟-1-甲基-4-氧代-7-(哌嗪-1-基)-4H- [1,3]噻嗪[3,2-a]喹啉-3-羧酸的N-取代衍生物:合成和抗菌活性。方法:在本研究中,N-取代的6-氟-1-甲基-4-氧代-7-(哌嗪-1-基)-4H- [1,3]噻嗪并[3,2-a]喹啉的衍生物通过使用三乙胺和DMF制备-3-羧酸。通过添加四丁基溴化铵(TBAB)修改此程序,以促进在很少的反应中完成。使用Morwet-D425可以促进上述两种方法均未进行的其他反应。所有新标题化合物均以其光谱数据为特征,并筛选了抗菌活性。结果:使用我们在美国专利第8号410,268B2中公开的方法合成了一些报道的化合物。在我们目前的工作中,我们已经获得了良好的产量和纯度。许多化合物表现出显着的抗菌活性。结论:可以推断,带有取代的苯基和喹啉环的标题化合物显示出与标准品相当的抗菌活性

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