Issue 3, 2014

Cascade synthesis of quinazolinones from 2-aminobenzonitriles and aryl bromides via palladium-catalyzed carbonylation reaction

Abstract

A cascade synthesis of quinazolinones from 2-aminobenzonitriles and aryl bromides through a palladium-catalyzed carbonylation reaction has been developed. Various quinazolinones were produced in moderate to excellent yields. The reactions go through aminocarbonylation of aryl bromides–hydration of nitriles–cyclization sequence. Notably, all the products were isolated by recrystallization.

Graphical abstract: Cascade synthesis of quinazolinones from 2-aminobenzonitriles and aryl bromides via palladium-catalyzed carbonylation reaction

Supplementary files

Article information

Article type
Paper
Submitted
08 Oct 2013
Accepted
06 Nov 2013
First published
07 Nov 2013

Green Chem., 2014,16, 1336-1343

Cascade synthesis of quinazolinones from 2-aminobenzonitriles and aryl bromides via palladium-catalyzed carbonylation reaction

H. Li, L. He, H. Neumann, M. Beller and X. Wu, Green Chem., 2014, 16, 1336 DOI: 10.1039/C3GC42089B

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