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Reduction of 9-aminoarylacridines and their salts

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

9-Formamidoarylacridans are obtained in the reduction of 9-aminoarylacridines with a free amino group by means of formic acid in the presence of triethylamine. Under these conditions N,N-dialkyl derivatives are cleaved to 9-unsubstituted acridan and dialkylanilines.

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Literature cited

  1. V. L. Rusinov, O. N. Chupakhin, V. A. Trofimov, M. I. Kollegova, and I. Ya. Postovskii, Khim. Geterotsikl. Soedin., 216 (1972).

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  3. V. L. Rusinov, O. N. Chupakhin, I. Ya. Postovskii, and L. M. Osenova, Khim. Geterotsikl. Soedin., 1291 (1973).

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Authors and Affiliations

  1. S. M. Kirov Ural Polytechnic Institute, Sverdlovsk

    O. N. Chupakhin, I. Ya. Postovskii, V. L. Rusinov & L. I. Mikisheva

Authors
  1. O. N. Chupakhin
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  2. I. Ya. Postovskii
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  3. V. L. Rusinov
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  4. L. I. Mikisheva
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Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 814–816, June, 1975.

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Chupakhin, O.N., Postovskii, I.Y., Rusinov, V.L. et al. Reduction of 9-aminoarylacridines and their salts. Chem Heterocycl Compd 11, 711–713 (1975). https://doi.org/10.1007/BF00959969

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  • DOI: https://doi.org/10.1007/BF00959969

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