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AN EFFICIENT METHOD FOR ACCESSING CARBOANNULATED AND FUNCTIONALIZED [1,2,3]TRIAZOLO[4,5- b ]PYRIDINES

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4-(N-Boc-amino)-1,2,3-triazole-5-carbaldehydes upon heating under reflux in acetic acid in the presence of pyrrolidine react with cycloalkanones, acetylacetone, 1,3-cyclohexanediones, and malononitrile resulting in annulation of the pyridine ring with the formation… Click to show full abstract

4-(N-Boc-amino)-1,2,3-triazole-5-carbaldehydes upon heating under reflux in acetic acid in the presence of pyrrolidine react with cycloalkanones, acetylacetone, 1,3-cyclohexanediones, and malononitrile resulting in annulation of the pyridine ring with the formation of new derivatives of [1,2,3]triazolo[4,5-b]pyridine.

Keywords: efficient method; carboannulated functionalized; triazolo pyridines; method accessing; functionalized triazolo; accessing carboannulated

Journal Title: Chemistry of Heterocyclic Compounds
Year Published: 2020

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