Abstract: | The reaction of 2-amino- and 2,4-diamino-sym-triazines with nitrourea and phenyl isocyanate was studied; it gives N-mono- and N,N -disubstituted ureas that contain sym-triazine segments. General features were established for the decomposition of carbamide derivatives of sym-triazine under electron impact.For communication 4, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 356–362, March, 1987. |