Issue 41, 2024

Cyclocondensation of o-phenylenediamines with α-ketothioesters: a novel approach for the synthesis of 2-acylbenzimidazoles

Abstract

We herein present a novel and an unexpected method for the synthesis of α-ketothioesters by the reaction of pyrrolidine with α-oxodithioesters followed by treatment with methyl iodide in methanol. One of the synthetic applications of α-ketothioesters for the synthesis of 2-acylbenzimidazoles by acid-catalyzed cyclocondensation with benzene-1,2-diamines is described. The probable mechanisms of formation of α-ketothioesters and 2-acylbenzimidazoles are proposed.

Graphical abstract: Cyclocondensation of o-phenylenediamines with α-ketothioesters: a novel approach for the synthesis of 2-acylbenzimidazoles

Supplementary files

Article information

Article type
Paper
Submitted
10 Jul 2024
Accepted
19 Sep 2024
First published
02 Oct 2024

New J. Chem., 2024,48, 17998-18003

Cyclocondensation of o-phenylenediamines with α-ketothioesters: a novel approach for the synthesis of 2-acylbenzimidazoles

K. Kavya, K. V. Honnabandar, B. T. Sridhar, T. R. Swaroop, A. Shivakumar and K. Mantelingu, New J. Chem., 2024, 48, 17998 DOI: 10.1039/D4NJ03105A

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