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Synthesis 2016; 48(09): 1389-1398
DOI: 10.1055/s-0035-1560416
DOI: 10.1055/s-0035-1560416
paper
Synthesis of Quinazolines and Dihydroquinazolines: o-Iodoxybenzoic Acid Mediated Tandem Reaction of o-Aminobenzylamine with Aldehydes
Further Information
Publication History
Received: 31 December 2015
Accepted after revision: 08 February 2016
Publication Date:
11 March 2016 (online)
Abstract
We have demonstrated a facile synthesis of diversely substituted quinazolines and 3,4-dihydroquinazolines through the o-iodoxybenzoic acid (IBX) mediated tandem reaction of readily available o-aminobenzylamine and aldehydes. The yield of the reactions generally ranged from 70% to 95%. This mild protocol provides an efficient strategy toward the synthesis of these classes of heterocycles.
Key words
quinazolines - dihydroquinazolines - o-iodoxybenzoic acid - o-aminobenzylamine - aldehydesSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1560416.
- Supporting Information
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