Issue 16, 2024

Guanidine hydrochloride (GuHCl)-catalysed microwave-mediated solvent- and metal-free synthesis of pyrimido[1,2-a]benzimidazole from aryl aldehyde and aryl methyl ketone

Abstract

A novel microwave-mediated synthesis method was developed for the rapid and eco-friendly production of pyrimido[1,2-a]benzimidazole in high yields utilizing simple and cost-effective starting materials. This reaction was facilitated by the green organocatalyst guanidine hydrochloride. This protocol offers a metal-free and organocatalysed technique to afford a library of highly fluorescent pyrimido[1,2-a]benzimidazole derivatives. Key features of this synthetic method include its broad compatibility with functional groups, operational simplicity, and scalability, making it a promising technique for various applications.

Graphical abstract: Guanidine hydrochloride (GuHCl)-catalysed microwave-mediated solvent- and metal-free synthesis of pyrimido[1,2-a]benzimidazole from aryl aldehyde and aryl methyl ketone

Supplementary files

Article information

Article type
Paper
Submitted
20 Mar 2024
Accepted
03 Jul 2024
First published
03 Jul 2024

Green Chem., 2024,26, 9230-9240

Guanidine hydrochloride (GuHCl)-catalysed microwave-mediated solvent- and metal-free synthesis of pyrimido[1,2-a]benzimidazole from aryl aldehyde and aryl methyl ketone

R. Jagdale, M. Z. Hussain, K. Goswami, R. Peraman and A. Jana, Green Chem., 2024, 26, 9230 DOI: 10.1039/D4GC01363H

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