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Formation of sym-triazines by the reaction of acyl isocyanates with benzamidine

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

2-Hydroxy-1,3,5-triazines containing aryl or alkyl substituents in the 4,6 positions have been obtained only recently by the action on amidines of N-(α-chloroalkylidene)carbamoyl chlorides [1] or N-acylimidic esters [2].

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Literature cited

  1. E. Degener, H. G. Schmelzer, and H. Holtschmidt, Angew. Chem. Inst. Ed., 5, 960 (1966).

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  2. M. Bel-Gacem Baccar, Compt. Rend., Ser. C, 264, 352 (1967).

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  3. A. Pinner, Ber., 23, 2923 (1890).

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Authors and Affiliations

  1. All-Union Scientific-Research Institute for Chemical Plant Protecting Agents, Moscow

    K. A. Nuridzhanyan, N. E. Mironova & L. M. Nesterova

Authors
  1. K. A. Nuridzhanyan
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  2. N. E. Mironova
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  3. L. M. Nesterova
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii.Vol. 6,No. 7,pp. 1001–1002, July, 1970.

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Nuridzhanyan, K.A., Mironova, N.E. & Nesterova, L.M. Formation of sym-triazines by the reaction of acyl isocyanates with benzamidine. Chem Heterocycl Compd 6, 932–933 (1970). https://doi.org/10.1007/BF00471695

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  • DOI: https://doi.org/10.1007/BF00471695

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