960化工网
A convenient palladium-catalyzed carbonylative synthesis of quinazolines from 2-aminobenzylamine and aryl bromides†
Jianbin Chen,Kishore Natte,Helfried Neumann,Xiao-Feng Wu
RSC Advances Pub Date : 10/24/2014 00:00:00 , DOI:10.1039/C4RA11303A
Abstract

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.

Graphical abstract: A convenient palladium-catalyzed carbonylative synthesis of quinazolines from 2-aminobenzylamine and aryl bromides
平台客服
平台客服
平台在线客服