The Journal of Organic Chemistry · 2024 · 14 citations · 46 references
Natural SciencesChemical EngineeringChemistryBiocatalysisCatalysisOrganic ChemistryCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MaterialsHeterocycle SynthesisRetrosynthetic AnalysisAlkylation ReactionsAlkyne ActivationChemical Synthesis PlanningMetathesis CatalysisSubstrate Scope
2-Methylquinazolin-4(3 H )-ones were efficiently constructed using solid calcium carbide as an alkyne source, 2-aminobenzamides or 2-aminobenzohydrazides as substrates, and p -tolylsulfonyl azide as a mediator through simultaneous formation of two C–N bonds in one step. The salient features of this protocol are the use of an inexpensive, abundant and easy-to-use alkyne source as a substitute for flammable and explosive gaseous acetylene, low-cost catalyst, wide substrate scope, satisfactory yield, and simple manipulation. This method can also be extended to gram scale.
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