Bekhit A A, Habib N S, Park Ji Young
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Alexandria, Alexandria, Egypt.
Boll Chim Farm. 2004 Jan-Feb;143(1):34-9.
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.
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。