Synthesis and In-vitro Antimicrobial Activity of Secondary and Tertiary Amines Containing 2-Chloro-6-methylquinoline Moiety
作者:Suresh Kumar、Sandhya Bawa、Darpan Kaushik、Bibhu P. Panda
DOI:10.1002/ardp.201000352
日期:2011.7
A number of secondary and tertiary amines bearing 2‐chloro‐6‐methylquinoline were synthesized by nucleophilic substitution reaction of 3‐(chloromethyl)‐2‐chloro‐6‐methylquinoline with substituted aromatic primary and secondary amines in presence of catalytic amount of triethylamine (TEA) and K2CO3. All the compounds were characterized by combined use of IR, 1H‐NMR, 13C‐NMR, mass spectral data, and
通过3-(氯甲基)-2-氯-6-甲基喹啉与取代的芳香伯胺和仲胺在催化量的三乙胺存在下的亲核取代反应,合成了许多带有2-氯-6-甲基喹啉的仲胺和叔胺( TEA) 和 K2CO3。所有化合物均通过 IR、1H NMR、13C NMR、质谱数据和微量分析的组合进行表征。在体外筛选新合成的喹啉胺对黑曲霉 MTCC 281、黄曲霉 MTCC 277、红曲霉 MTCC 369、柑橘青霉 NCIM 768 的抗真菌活性和抗菌活性菌株,即。通过琼脂扩散技术检测大肠杆菌 NCTC 10418、金黄色葡萄球菌 NCTC 65710 和铜绿假单胞菌 NCTC 10662。