Issue 7, 2019

An efficient, mild and metal free l-proline catalyzed construction of fused pyrimidines under microwave conditions in water

Abstract

One-pot condensation of 4-hydroxy coumarins, aldehydes and urea/thiourea to build C–C and C–N bonds is described. Fused pyrimidines have been synthesized under mild reaction conditions using L-proline. The protocol has been performed rapidly and efficiently in water under metal free conditions. Heterocyclic derivatives have been synthesized using the present methodology and avoid the use of hazardous solvents over conventional organic solvents. A proposed mechanism could be established for three component reactions. The present study reveals the first case in which L-proline has been explored as a homogeneous catalyst in the synthesis of fused pyrimidines in water under microwave irradiation. This synthesis involves simple workup and acceptable efficiency. The most notable feature of this protocol is the ability of the catalyst to influence asymmetric induction in the reaction.

Graphical abstract: An efficient, mild and metal free l-proline catalyzed construction of fused pyrimidines under microwave conditions in water

Supplementary files

Article information

Article type
Paper
Submitted
09 Sep 2018
Accepted
10 Jan 2019
First published
04 Feb 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 3755-3763

An efficient, mild and metal free L-proline catalyzed construction of fused pyrimidines under microwave conditions in water

M. S. Kaurav, P. K. Sahu, P. K. Sahu, M. Messali, Saud M. Almutairi, P. L. Sahu and D. D. Agarwal, RSC Adv., 2019, 9, 3755 DOI: 10.1039/C8RA07517D

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