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A convenient palladium-catalyzed carbonylative synthesis of quinazolines from 2-aminobenzylamine and aryl bromides

机译:由2-氨基苄胺和芳基溴化物方便地钯催化羰基合成喹唑啉

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摘要

A novel and practical strategy towards quinazoline scaffolds synthesis has been achieved. Through palladium-catalyzed carbonylative coupling of 2-aminobenzylamine with aryl bromides, the desired quinazolines were produced in moderate to good yields for the first time. The reactions followed an aminocarbonylation-condensation-oxidation sequence in a one-pot one-step manner. Preliminary investigation showed DMSO serves both as solvent and oxidant in this procedure.
机译:已经实现了新颖且实用的喹唑啉支架合成策略。通过2-氨基苄基胺与芳基溴化物的钯催化羰基化偶联,首次以中等至良好的收率生产了所需的喹唑啉。反应以一锅一步的方式遵循氨基羰基化-缩合-氧化顺序。初步研究表明,DMSO在此过程中既充当溶剂又充当氧化剂。

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