Abstract
Derivatives of 1-benzyl-4-pyrimidinones and 1-benzyl-6-pyrimidinones were synthesized by the reaction of β-cyano-3-N-benzylaminocrotonamide and α-cyano-β-aminocrotonic acid N-benzylamine with dimethylformamide diethylacetal. When 1-benzyl-5-cyano-6-(β-dimethylamino)vinyl-1,6-dihydro-4-pyrimidinone is heated in an alkaline medium, it is converted to 3-cyano-4-benzylamino-2-pyridone, from which a pyrido[1,2-a]pyrimidine derivative was synthesized. When 1-benzyl-5-cyano-4-(β-dimethylamino) vinyl-1,6-dihydro-6-pyrimidinone is heated in alkaline solution, it is converted to α-cyano-β-hydroxycrotonic acid N-benzylamide.
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See [1] for Communication 37.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 816–820, June, 1983.
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Granik, V.G., Kaimanakova, S.I. Acetals of lactams and acid amides. 38. Synthesis of pyrimidine and pyridine derivatives on the basis of the reaction of enamino amides with amide acetals. Chem Heterocycl Compd 19, 657–661 (1983). https://doi.org/10.1007/BF00523081
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DOI: https://doi.org/10.1007/BF00523081