Issue 3, 2011

Microwave-promoted efficient synthesis of dihydroquinazolines

Abstract

A solvent- and catalyst-free synthesis of dihydroquinazolines is described. 2,4-Disubstituted-1,2-dihydroquinazolines can be readily obtained from 2-aminobenzophenone and aldehydes under microwave irradiation using urea as an environmentally benign source of ammonia, with a small amount of the corresponding quinazolines as the minor product. The reaction is simple, clean and excellent yields are obtained within minutes.

Graphical abstract: Microwave-promoted efficient synthesis of dihydroquinazolines

Supplementary files

Article information

Article type
Paper
Submitted
22 Nov 2010
Accepted
16 Dec 2010
First published
01 Feb 2011

Green Chem., 2011,13, 718-722

Microwave-promoted efficient synthesis of dihydroquinazolines

R. Sarma and D. Prajapati, Green Chem., 2011, 13, 718 DOI: 10.1039/C0GC00838A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements