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Preparation of 3,4-Substituted-5-Aminopyrazoles and 4-Substituted-2-Aminothiazoles
24
Citations
60
References
2018
Year
Medicinal ChemistryDiversity Oriented SynthesisDerivativesDerivative (Chemistry)Suzuki CouplingNatural SciencesDrug DiscoveryDiversity-oriented SynthesisMedicineOrganic ChemistryHeterocycle ChemistryPharmacologyPalladium-mediated α-ArylationSynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringDrug Discovery Projects
3,4-Substituted-5-aminopyrazoles and 4-substituted-2-aminothiazoles are frequently used intermediates in medicinal chemistry and drug discovery projects. We report an expedient flexible synthesis of 3,4-substituted-5-aminopyrazoles (35 examples), based on palladium-mediated α-arylation of β-ketonitriles with aryl bromides. A library of 4-substituted-2-aminothiazoles (21 examples) was assembled by a sequence employing Suzuki coupling of newly prepared, properly protected pinacol ester and MIDA ester of 4-boronic acid-2-aminothiazole with (hetero)aryl halides.
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