Abstract

AbstractAn electrochemical dehydrogenative C−H/N−H cross coupling of imidazopyridines with diarylamines has been developed. A variety of triarylamine derivatives could be obtained in high regioselectivities and moderate‐to‐good yields. In this transformation, the reaction is conducted in a simple undivided cell without using a metal catalyst or a stoichiometric amount of external chemical oxidants. Mechanistic studies indicate that the C−N bond is likely to be formed through the cross coupling between an arene cation radical and a nitrogen radical.

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