Abstract
Treatment of 2-(N-potassium-N-cyanamino)-4,6-dimethylpyrimidine with ethyliodoacetate produces 2-(N-cyano-N-carbethoxymethylamino)-4,6-dimethylpyrimidine. Alkaline hydrolysis of the last gives 2-(3-potassium-2,4-dioxoimidazolidinyl-1)-4,6-dimethylpyrimidine. Ammonolysis and hydrazinolysis give imino- or amino-imidazolidinylpyrimidine, respectively.
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Additional information
Armenian Agricultural Institute, Erevan 375009. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1239–1241, September, 1994. Original article submitted August 9, 1994.
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Dovlatyan, V.V., Éliazyan, K.A. & Pivazyan, V.A. Functionally substituted azines. 1. Synthesis and reactions of 2-(N-cyano-N-carbethoxmethylamino)-4,6-dimethylpyrimidine. Chem Heterocycl Compd 30, 1074–1076 (1994). https://doi.org/10.1007/BF01171168
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DOI: https://doi.org/10.1007/BF01171168