Issue 95, 2022

Ketone-derived 2,3-dihydroquinazolinones in N-heteroarene C–H alkylation via C–C bond scission under oxidative metal catalysis

Abstract

A silver-catalysed oxidative sp2 C–H alkylation of N-heteroarenes with ketone-derived 2,3-dihydroquinazolinones at room temperature is developed. The combination of a metal catalyst and perdisulfate oxidant promotes the rarely explored thermal activation of pre-aromatic 2,3-dihydroquinazolinone to generate an alkyl radical, supported by mechanistic studies. In addition to the broad scope, good functionality tolerance, late stage functionalization of APIs, and synthesis of a novel Papaverine analogue, the utilization of an N-heteroarene C–H bond and ketone as a non-trivial alkyl radical source represents the salient feature of this method.

Graphical abstract: Ketone-derived 2,3-dihydroquinazolinones in N-heteroarene C–H alkylation via C–C bond scission under oxidative metal catalysis

Supplementary files

Article information

Article type
Communication
Submitted
07 Sep 2022
Accepted
25 Oct 2022
First published
26 Oct 2022

Chem. Commun., 2022,58, 13202-13205

Ketone-derived 2,3-dihydroquinazolinones in N-heteroarene C–H alkylation via C–C bond scission under oxidative metal catalysis

P. P. Mondal, A. Pal, A. K. Prakash and B. Sahoo, Chem. Commun., 2022, 58, 13202 DOI: 10.1039/D2CC04947C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements