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Intramolecular Copper(I)‐Catalyzed Interrupted Click–Acylation Domino Reaction
Author(s) -
Larin Egor M.,
Lautens Mark
Publication year - 2019
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201907448
Subject(s) - acylation , chemistry , cycloaddition , intramolecular force , combinatorial chemistry , catalysis , alkyne , azide , click chemistry , domino , copper , organic chemistry
Acyl substituted triazoles are valuable scaffolds, but the direct synthesis of these moieties from terminal alkynes by copper catalysis remains unexplored. We report a robust, general, and efficient method using a simple CuI/2,2′‐bipyridine catalytic system. This transformation involves a copper catalyzed azide‐alkyne cycloaddition (CuAAC) followed by an intramolecular acylation onto a carbamoyl chloride. The reaction proceeds under mild conditions, tolerates several functional groups, and is readily scalable. This method represents a novel strategy towards the synthesis of complex heterocycles by a CuAAC/acylation domino process.

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