Journal
SYNLETT
Volume -, Issue 11, Pages 1606-1608Publisher
GEORG THIEME VERLAG KG
DOI: 10.1055/s-0029-1219962
Keywords
imidazo[1,2-a]pyridines; pyridines; alpha-bromoketones; ammonium acetate; microwave irradiation; solvent-free synthesis; cyclizations; heterocycles
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Funding
- Research Council of University of Tehran [6102036/1/03]
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A novel and efficient synthesis of imidazo[1,2-a]pyridines is described. N-Phenacylpyridinium bromides, which were prepared in situ from the addition of pyridines to alpha-bromoketones, undergo nucleophilic addition of ammonium acetate under microwave irradiation and solvent-free conditions to afford the corresponding imidazo[1,2-a]pyridines in excellent yields.
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