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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V. V. Dovlatyan, É. N. Ambartsumyan, and L. A. Khachatryan, Arm. Khirn. Zh., 33, 311 (1980).
V. V. Dovlatyan, L. A. Khachatryan, and É. N. Ambartsumyan, Arm. Khim. Zh., 35, 684 (1982).
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