Antimicrobial Evaluation and Efficient Green Synthesis of 8-Substituted-2,5-dihydro-1,5-benzothiazepine Derivatives

P. Sharma
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引用次数: 0

Abstract

8-Substituted-2,5-dihydro-1,5-benzothiazepine derivatives have been synthesized by the reaction of 1-(2-furyl)-3-(3,4-dimethoxyphenyl)-2-propenone with six 5-substiuted-2-minobenzenethiols in dry ethanol saturated with dry HCl gas and also in the presence of aluminium nitrate as catalyst in dry ethanol. All the newly synthesized compounds were characterized by analytical and spectral data comprising IR, 1H NMR, 13C NMR, 19F NMR and mass studies. All these compounds have also been evaluated for their antimicrobial assay against the Gram-positive bacteria, Staphylococcus aureus and the Gram-negative bacteria, Pseudomonas aeruginosa and the fungus, Candida albicans. The antifungal activity was found to be more significant than antibacterial activity.
8-取代-2,5-二氢-1,5-苯并噻唑类衍生物的抗菌评价及高效绿色合成
以6个5-取代-2-氨基苯乙醇与1-(2-呋喃基)-3-(3,4-二甲氧基苯基)-2-丙烯为原料,在干燥乙醇中以干HCl气体饱和和硝酸铝为催化剂的条件下,合成了8-取代-2,5-二氢-1,5-苯并噻吩衍生物。所有新合成的化合物都通过IR, 1H NMR, 13C NMR, 19F NMR和质量研究等分析和光谱数据进行了表征。所有这些化合物还对革兰氏阳性菌金黄色葡萄球菌和革兰氏阴性菌铜绿假单胞菌和真菌白色念珠菌进行了抗菌试验评价。抗真菌活性比抗菌活性更显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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