This method shows effective ortho-C-H alkynylation of anilides with bromoalkynes, highlighting broad substrate scope and versatility.
A straightforward and efficient Cp*Co(III)-catalyzed ortho-C-H alkynylation of anilides with diverse readily available bromoalkynes was developed in which the weakly coordinating amide carbonyl group served as the directing group. This strategy provides a practical route for the synthesis of ortho-alkynylanilines, featuring good functional group tolerance and a broad substrate scope. Aryl-, alkyl-, and silyl-substituted bromoalkynes are compatible substrates in this catalytic system. Furthermore, subsequent synthetic transformations of the products demonstrate the synthetic utility of this methodology.
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Yu et al. (2025) studied this question.
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