Abstract
Base-promoted reactions of benzotriazolyl-containing acetic acid derivatives, 2-(benzotriazol-1-yl)acetonitrile (7a), 2-(benzotriazol-1-yl)acetamide (7b), and (±)-2-(benzotriazol-1-yl)propionamide (7c), with α,β-unsaturated ketones 8 give efficient and regioselective access to previously difficult to attain 3-unsubstituted pyridine derivatives: the 2-(substituted amino)pyridines 14a-k and the 4,6-substituted pyrid-2-ones 15a-h. The pyridine rings result from tandem [3 + 3] annulations involving a Michael addition followed by cyclization.
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CITATION STYLE
Katritzky, A. R., Belyakov, S. A., Sorochinsky, A. E., Henderson, S. A., & Chen, J. (1997). Benzotriazole-Assisted Preparations of 2-(Substituted amino)pyridines and Pyrid-2-ones. Journal of Organic Chemistry, 62(18), 6210–6214. https://doi.org/10.1021/jo970561h
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