Issue 13, 2024

Electro-oxidative intermolecular CSP2–H amination of heteroarenes via proton-coupled electron transfer

Abstract

A new electrochemical proton-coupled electron transfer method for the intermolecular CSP2–H amination of heteroarenes without oxidants, metal catalysts and external electrolytes has been developed. Various new N-containing heteroarenes were prepared in medium to high yields, and the indole-containing product could be converted into practical 2-oxindole by simple basic hydrolysis. Mechanistic investigation indicated that ester sulfonyl-substituted N-radicals could be formed by the combination of 2,6-lutidine and electrochemical oxidation, which is the key to achieve the desired chemoselectivity.

Graphical abstract: Electro-oxidative intermolecular CSP2–H amination of heteroarenes via proton-coupled electron transfer

Supplementary files

Article information

Article type
Communication
Submitted
31 Jan 2024
Accepted
28 Feb 2024
First published
29 Feb 2024

Org. Biomol. Chem., 2024,22, 2549-2553

Electro-oxidative intermolecular CSP2–H amination of heteroarenes via proton-coupled electron transfer

S. Liu, X. Liu, T. Zhang, X. Bao, X. Sheng, Z. Qi and D. Jiang, Org. Biomol. Chem., 2024, 22, 2549 DOI: 10.1039/D4OB00164H

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