文摘

(合成及抗菌活性3-chloro-4) - substitutedphenyl -azetidinonyl / thiazolidinonyl-4 - (3-acetanilido) oxa /噻唑

作者(年代):Kaur Indu辛格,Hemlata Sunil Kumar Arun Kumar Ashok Kumar

Cyclocandensation 2 - [(substitutedbenzylidene)氨基]4 - (3 - acetanilido)唑(3 a-3j)和2 - [(substitutedbenzylidene)氨基]4 - (3 - acetanilido)噻唑(7 a-7j)和氯乙酰氯为n - 2 - [3 - chloro-4 (substitutedphenyl) 2-oxoazetidin-1-yl] 4 - (3-acetanilido)唑(4 a-4j)和n - [3-chloro-4 - (substitutedphenyl) 2-oxoazetidin-1-yl] 4 - (3 - acetanilido)噻唑(8 a-8j) respectively.N-2 - [2 - (substitutedphenyl) 4-oxo 1-thiazolidinyl] 4 - (3-acetanilido)唑(5 a-5j)和n - [2 - (substitutedphenyl) 4-oxo-1-thiazolidinyl] 4 - (3-acetanilido)唑(5 a-5j)合成了化合物(3 a-3j)和反应(7 a-7j)与巯基乙酸在无水氯化锌的存在。所有的合成化合物筛选抗菌活性并与参考药物氨苄青霉素和环丙沙星。本系列的compoundwas最有效的化合物。所有合成的化合物的结构特征是元素(C、H、N)和光谱(IR和1 H NMR)分析。