Synthesis and biological evaluation of some drug-like scaffolds of benzo- and pyrido-fused medium-sized N-heterocycles obtained via intramolecular Friedel–Crafts acylation reactions Scientific paper
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Abstract
An unprecedented, concise and environmentally-friendly protocol for the synthesis of benzo-and pyrido-annulated azocinones, azoninones and azecinones 8a–h via Friedel–Crafts reactions is described. These simple and efficient procedures involve cycliacylations of heterocyclic esters 7a–h in the presence of catalytic amount of AlCl3/CH3NO2 or TfOH or PPA catalysts as the key step. Starting amides 3a–d were readily obtained by coupling reactions of acryloyl chlorides 2a and b with pyridin-2-amines 1a and b. Developed strategy offers some high selectivity reactions, mild reaction conditions and easy access to complex medium-sized N-heterocycles in moderate to good yields. All tetracyclic fused compounds have been screened for antimicrobial activity.
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