A one pot, three component synthesis of coumarin hybrid thiosemicarbazone derivatives and their antimicrobial evolution

Rajesh H. Vekariya , Kinjal D. Patel , Dhanji P. Rajani , Smita D. Rajani , Hitesh D. Patel
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引用次数: 21

Abstract

A convenient, one-pot, multi-component protocol for the preparation of 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinecarbothioamide derivatives has been achieved. Here, firstly we have reported the synthesis of 3-acetyl-2H-chromen-2-one using starch sulfuric acid and cellulose sulfuric acid as biodegradable catalysts. Subsequently, we also carried out the reaction of isothiocynates, hydrazine hydrate and 3-acetyl-2H-chromen-2-one in the presence of catalytic amount of glacial acetic acid in refluxing ethanol to afford corresponding 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene)hydrazinecarbothioamide derivatives in high to excellent yields. All synthesized compounds were screened for antimicrobial activity. All compounds were found to show good to excellent activity against Escherichia coli MTCC 443.

香豆素杂化硫代氨基脲衍生物的一锅三组分合成及其抑菌进化
实现了一种简便、一锅、多组分制备2-(1-(2-氧- 2h -铬-3-基)乙基)肼碳硫酰胺衍生物的方法。本文首先报道了以淀粉硫酸和纤维素硫酸为生物降解催化剂合成3-乙酰基- 2h -铬-2- 1。随后,我们还在冰醋酸的催化量下,在回流乙醇中进行了异硫辛酸盐、水合肼和3-乙酰基- 2h -铬-2- 1的反应,得到了相应的2-(1-(2-氧- 2h -铬-3-基)乙基)肼碳硫酰胺衍生物,收率高至优。所有合成的化合物都进行了抗菌活性筛选。所有化合物对大肠杆菌MTCC 443均表现出良好至优异的活性。
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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