含药效基团取代喹唑啉类化合物的合成

Harutyunyan Artur A
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引用次数: 1

摘要

对生物活性喹唑啉衍生物合成的持续研究[1,2]在本报告中,我们描述了以前未知的取代2-甲基喹唑啉和2-[2-芳基(己基)乙烯基]喹唑啉的合成,它们在环的不同位置含有药效团。2-甲基- 4h -3,1-苯并恶辛- 1,1a, b与芳香胺和杂环胺相互作用,按照方案1进行合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Substituted Quinazolines Containing Pharmacophoric Groups
Continuing research on the synthesis of biologically active quinazoline derivatives [1,2] in this report we have described the synthesis of previously unknown substituted 2-methylquinzolins and 2-[2-aryl(hetaryl)vinyl]quinazolines, which contain pharmacophore groups at different positions of the ring. Synthesis was carried out by the interaction of 2-methyl-4H-3,1-benzoxzin4-ones 1a, b with aromatic and heterocyclic amines, according to the Scheme 1.
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