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Synthesis of N-cyano-N-alkoxycarbonylalkylamino-symm-triazines and their solvolysis

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The action of potassium salts of cyanoamino-symm-triazines on esters of chloroacetic and bromomalonic acids gave carbonylalkylamino-symm-triazines. The solvolysis of these esters proceeds with heterocyclilzation, leading to the formation of hydantoin derivatives.

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References

  1. V. V. Dovlatyan, É. N. Ambartsumyan, and L. A. Khachatryan, Arm. Khirn. Zh., 33, 311 (1980).

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  3. V. V. Dovlatyan, L. A. Khachatryan, and É. N. Ambartsumyan, Arm. Khim. Zh., 35, 799 (1982).

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1114–1116, August, 1993.

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Dovlatyan, V.V., Ambartsumyan, É.N., Gyul'budagyan, L.L. et al. Synthesis of N-cyano-N-alkoxycarbonylalkylamino-symm-triazines and their solvolysis. Chem Heterocycl Compd 29, 949–951 (1993). https://doi.org/10.1007/BF00534276

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  • DOI: https://doi.org/10.1007/BF00534276

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