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Indole derivatives.

CVI. Synthesis of mercapto derivatives of tryptamine

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Chemistry of Heterocyclic Compounds Aims and scope

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Abstract

The nature of the products of reduction of nitro compounds of the indole series containing a polysulfide chain depends on the length of the latter. In mono- and disulfides only the nitro groups are reduced, and diamino monosulfides and diamino disulfides are formed. In the reduction of the dinitro trisulfide the chain is cleaved and an amino thiol is formed. The reduction of acetylthionitro compounds is accompanied by migration of the S-N bond, as a result of which an acetamido thiol is formed.

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Literature cited

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Authors and Affiliations

  1. S. Ordzhonikidze All-Union Scientific-Research Pharmaceutical-Chemistry Institute, Moscow

    O. D. Shalygina, L. Kh. Vinograd & N. N. Suvorov

Authors
  1. O. D. Shalygina
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  2. L. Kh. Vinograd
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  3. N. N. Suvorov
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Additional information

See [1] for communication CV.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 795–797, June, 1975.

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Shalygina, O.D., Vinograd, L.K. & Suvorov, N.N. Indole derivatives.. Chem Heterocycl Compd 11, 693–695 (1975). https://doi.org/10.1007/BF00959964

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  • DOI: https://doi.org/10.1007/BF00959964

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