Abstract
The reaction of 1,1,1-trifluoro-2-phenyl-2,4,6,6-tetrachloro-3,5-diazahexa-3,5-diene with primary amines proceeds via two pathways and leads to 1,2-dihydro-1,3,5-triazines or the corresponding carbodiimides. The reaction pathway is determined by the steric characteristics of the amines.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1249–1251, September, 1983.
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Fetyukhin, V.N., Vovk, M.V. Synthesis of symmetrical 1,2-dihydrotriazines by the reaction of 1,1,1-trifluoro-2-phenyl-2,4,6,6-tetrachloro-3,5-diazahexa-3,5-diene with primary amines. Chem Heterocycl Compd 19, 1001–1003 (1983). https://doi.org/10.1007/BF00506889
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DOI: https://doi.org/10.1007/BF00506889