4(3H)-喹唑啉酮的噻唑基和噻二唑基衍生物的合成及其抗炎抗菌作用。

Bollettino chimico farmaceutico Pub Date : 2004-01-01
A A Bekhit, N S Habib, Ji Young Park
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引用次数: 0

摘要

本文介绍了4(3H)-喹唑啉酮衍生物的合成。第一个系列是由中间体3-芳基-2取代硫代氨基甲酰肼-4(3H)-喹唑啉酮2a,b与溴乙酸乙酯环化得到相应的噻唑啉基衍生物3a,b。第二系列是由中间体2a,b与苯那基溴或4取代苯那基溴环化得到噻唑啉基衍生物4a-f。然后,中间体2a,b与巯基乙酸反应得到噻唑烷基衍生物5a,b。另一方面,用乙酸酐加热中间体2a,b,得到相应的噻二唑啉基衍生物6a,b。一些合成的化合物显示出良好的抗炎抗菌活性。
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Synthesis of some thiazolyl and thiadiazolyl derivatives of 4(3H)-quinazolinone as anti-inflammatory-antimicrobial agents.

This paper describes the synthesis of four series of 4(3H)-quinazolinone derivatives. The first series was prepared by cyclization of the intermediate 3-aryl-2-substituted thiocarbamoylhydrazonomethyl-4(3H)-quinazolinones 2a,b with ethyl bromoacetate to afford the corresponding thiazolidinonyl derivatives 3a,b. The second series were prepared by the cyclization of the intermediate 2a,b with phenacyl bromide or 4-substituted phenacyl bromide giving rise to thiazolinyl derivatives 4a-f. Furthermore, the thiazolidinonyl derivatives 5a,b were obtained by reaction of the intermediate 2a,b with thioglycolic acid. On the other hand, heating the intermediate 2a,b with acetic anhydride afforded the corresponding thiadiazolinyl derivatives 6a,b. Some of the synthesized compounds showed promising anti-inflammatory-antimicrobial activities.

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