Efficient method synthesizes amide-substituted quinolines from o-alkynylisocyanobenzenes and nitriles, suggesting a novel pathway.
An efficient method for the synthesis of amide-substituted quinolines through silver/indium-catalyzed cyclization from o-alkynylisocyanobenzenes with nitriles has been reported. The reaction was initiated by the intramolecular cyclization of the o-alkynylisocyanobenzenes to generate the quinolyl cationic intermediate, followed by an intermolecular Ritter reaction with nitriles to give a nitrile-quinoline-based nitrilium salt, subsequently with hydrolysis to afford the amide-substituted quinolines.
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Liu et al. (2026) studied this question.
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