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Palladium-Catalyzed Chemoselective Monoarylation of Hydrazides for the Synthesis of [1,2,4]Triazolo[4,3-<i>a</i>]pyridines
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Citations
16
References
2010
Year
Chemical EngineeringEngineeringOrganic ChemistryMicrowave IrradiationCatalysisOrganometallic CatalysisPalladium-catalyzed Chemoselective MonoarylationChemistryHeterocycle ChemistryTerminal Nitrogen AtomSynthesis MethodSynthetic ChemistryAcetic Acid
An efficient and convenient method for the synthesis of [1,2,4]triazolo[4,3-a]pyridines was exemplified by the synthesis of 20 analogues bearing a variety of substituents at the 3-position. The methodology involves a palladium-catalyzed addition of hydrazides to 2-chloropyridine, which occurs chemoselectively at the terminal nitrogen atom of the hydrazide, followed by dehydration in acetic acid under microwave irradiation.
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