Abstract
The interaction of 6-nitroazolo[1,5-a]pyrimidines with ethyl cyanoacetate is accompanied by transformation of the pyrimidine ring, forming derivatives of 2-azolylaminopyrimidine. The structure of the transformation products has been investigated in crystals and in solution.
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For Communication 10, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1631–1637, December, 1990.
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Rusinov, V.L., Pilicheva, T.L., Tumashov, A.A. et al. Nitroazines 11. Structure of products of transformation OF 6-nitroazolo-[1,5-a]pyrimidines under the influence of cyanoacetic ester. Chem Heterocycl Compd 26, 1357–1362 (1990). https://doi.org/10.1007/BF00473963
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DOI: https://doi.org/10.1007/BF00473963