Suppr超能文献

4(3H)-喹唑啉酮的一些噻唑基和噻二唑基衍生物作为抗炎抗菌剂的合成

Synthesis of some thiazolyl and thiadiazolyl derivatives of 4(3H)-quinazolinone as anti-inflammatory-antimicrobial agents.

作者信息

Bekhit A A, Habib N S, Park Ji Young

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Alexandria, Alexandria, Egypt.

出版信息

Boll Chim Farm. 2004 Jan-Feb;143(1):34-9.

Abstract

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.

摘要

本文描述了四个系列4(3H)-喹唑啉酮衍生物的合成。第一系列是通过中间体3-芳基-2-取代硫代氨基甲酰腙甲基-4(3H)-喹唑啉酮2a、b与溴乙酸乙酯环化,得到相应的噻唑烷酮基衍生物3a、b。第二系列是通过中间体2a、b与苯甲酰溴或4-取代苯甲酰溴环化,得到噻唑啉基衍生物4a - f。此外,中间体2a、b与巯基乙酸反应得到噻唑烷酮基衍生物5a、b。另一方面,中间体2a、b与乙酸酐加热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有前景的抗炎抗菌活性。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验