Journal of Heterocyclic Chemistry · 1979 · 54 citations · 10 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryAmino Acid ChemistryMacrocycle SynthesisPyrazine ChemistryPyrazole ChemistryPyrazole SynthesisPyrimidine AnalogsPyrimidine AnaloguesPyrimidine Chemistry
Abstract Benzoylacetonitrile (II) reacted with trichloroacetonitrile (III) to yield the β‐amino‐β‐trichloromethylacrylonitrile IV. Compound IV reacted with hydrazine hydrate to yield 5‐amino‐4‐cyano‐3‐phenylpyrazole (V) and with 2‐aminopyridine to yield the aminopyridine derivative VIII ( cf ., Chart I). Compound IV reacted with III to yield 2,4‐bis(trichloromethyl)‐5‐cyano‐6‐phenylpyrimidine (I) which could be converted into a variety of pyrazolo[4,3‐ d ]pyrimidine derivatives by treatment with hydrazine hydrate under a variety of different experimental conditions ( cf ., Chart II).
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The structural studies of formycin and formycin b
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