Journal of Heterocyclic Chemistry · 2010 · 34 citations · 8 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic Synthesis
Abstract magnified image A “one‐pot” method for the synthesis of N ‐(1,3‐diphenyl‐1 H ‐pyrazol‐5‐yl)amides was developed by cyclization of benzoylacetonitrile ( 1 ) and phenylhydrazine in neat condition followed by acylation. The corresponding N ‐(1,3‐diphenyl‐1 H ‐pyrazol‐5‐yl)amides were provided in good to excellent yields (70–90%). The significant advantages of the new synthetic method are excellent yields and simple work‐up procedure without isolation and purification of intermediary 5‐amino‐1,3‐diphenyl pyrazol ( 2 ). J. Heterocyclic Chem., (2010).
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Comprehensive medicinal chemistry
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