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二氢呋喃并苯并恶唑啉-2(3H)-酮及其衍生物的合成与抗菌活性

Synthesis and antimicrobial activity of dihydrofurobenzoxazolin-2(3H)-ones and their derivatives.

作者信息

Bhalerao U T, Gawali B B, Annapurna J

机构信息

Organic Division II, Indian Institute of Chemical Technology, Hyderabad.

出版信息

Arzneimittelforschung. 1994 Sep;44(9):1077-9.

PMID:7986248
Abstract

A series of dihydrofurobenzoxazolin-2(3H)-ones and their derivatives were synthesized. The structures of the compounds have been elucidated by IR, mass, 1H-NMR spectra and elementary analysis. The in vitro activity of these compounds was investigated against Gram-positive and Gram-negative bacteria and also against Candida albicans. 7,7-Dimethyl-7,8-dihydro-furo[2,3-g]benzoxazolin-2(3H)-one (compound 2) proved to be more potent than compound 1. Compound 3 also showed significant activity against all the microbes tested. Compounds 4 and 5 were more effective against Gram-positive bacteria than Gram-negative bacteria but inactive against C. albicans.

摘要

合成了一系列二氢呋喃并苯并恶唑啉 -2(3H)- 酮及其衍生物。通过红外光谱、质谱、1H - 核磁共振光谱和元素分析对这些化合物的结构进行了阐明。研究了这些化合物对革兰氏阳性菌、革兰氏阴性菌以及白色念珠菌的体外活性。7,7 - 二甲基 -7,8 - 二氢 - 呋喃并[2,3 - g]苯并恶唑啉 -2(3H)- 酮(化合物2)被证明比化合物1更具活性。化合物3对所有测试的微生物也显示出显著活性。化合物4和5对革兰氏阳性菌的作用比对革兰氏阴性菌更有效,但对白色念珠菌无活性。

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