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Synthesis of heterocyclic compounds on the basis of carboxylic acid arylamides

III. Reactions with the participation of phenyliminooxalyl chloride

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The exchange and cyclization of phenyliminooxalyl chloride with ammonium thiocyanate, sodium azide, aniline, amidoximes, and diphenylthiourea, and with 2-aminopyridine, 2-aminobenzothiazole, and 2-amino- and 2-mercaptobenzimidazole were studied. The cyclization products are derivatives of thiazolidine, imidazo[1,2-a]pyridine, imidazo[2,1-b]benzothiazole, imidazo[1,2-a]benzimidazole, and thiazolo[3,2-a]benzimidazole. A trimer of 1-phenyltetrazole-5-carboxylic acid was obtained when an attempt was made to convert its azide to the corresponding isocyanate.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Academy of Sciences of the Ukrainian SSR, Kiev

    M. O. Lozinskii, A. F. Shivanyuk & P. S. Pel'kis

Authors
  1. M. O. Lozinskii
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  2. A. F. Shivanyuk
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  3. P. S. Pel'kis
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Additional information

See [1] for communication II.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 471–474, April, 1971.

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Lozinskii, M.O., Shivanyuk, A.F. & Pel'kis, P.S. Synthesis of heterocyclic compounds on the basis of carboxylic acid arylamides. Chem Heterocycl Compd 7, 439–442 (1971). https://doi.org/10.1007/BF00471480

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  • DOI: https://doi.org/10.1007/BF00471480

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