Issue 3, 2021

Peroxide-mediated synthesis of benzimidazo[2,1-a]isoquinoline-6(5H)-ones via cascade methylation/ethylation and intramolecular cyclization

Abstract

A metal-free oxidative radical methylation/arylation of 2-arylbenzoimidazoles with DTBP as the oxidant and methyl radical source was developed. The reaction proceeds through a sequential methyl radical addition/cyclization pathway and affords a series of methyl functionalized benzimidazo[2,1-a]isoquinoline-6(5H)-ones in moderate to good yields. Besides, the ethylation/arylation of 2-arylbenzoimidazoles was also achieved with DTAP.

Graphical abstract: Peroxide-mediated synthesis of benzimidazo[2,1-a]isoquinoline-6(5H)-ones via cascade methylation/ethylation and intramolecular cyclization

Supplementary files

Article information

Article type
Paper
Submitted
30 Nov 2020
Accepted
15 Dec 2020
First published
15 Dec 2020

Org. Biomol. Chem., 2021,19, 619-626

Peroxide-mediated synthesis of benzimidazo[2,1-a]isoquinoline-6(5H)-ones via cascade methylation/ethylation and intramolecular cyclization

C. Pan, C. Yuan and J. Yu, Org. Biomol. Chem., 2021, 19, 619 DOI: 10.1039/D0OB02383C

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