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Heterocyclic Thiones and Their Analogs in 1,3-Dipolar Cycloaddition Reactions: II. Reactions of Benzothiazole-2-thione with Nitrilimines

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Abstract

Benzothiazole-2-thione reacted with C,N-disubstituted nitrilimines to give the corresponding bis-[2-(1,3,4-thiadiazol-2-ylideneamino)phenyl] disulfides. In some cases, α-(1,3-benzothiazol-2-ylsulfanyl)-(α-R)-alkanone arylhydrazones were formed as by-products. The structure of the isolated compounds was proved by X-ray analysis.

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Authors
  1. O. V. Firsova
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  2. T. S. Dolgushina
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  3. V. A. Polukeev
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  4. V. E. Zavodnik
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  5. A. I. Stash
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  6. V. K. Bel'skii
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  7. V. A. Galishev
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Firsova, O.V., Dolgushina, T.S., Polukeev, V.A. et al. Heterocyclic Thiones and Their Analogs in 1,3-Dipolar Cycloaddition Reactions: II. Reactions of Benzothiazole-2-thione with Nitrilimines. Russian Journal of Organic Chemistry 40, 1018–1026 (2004). https://doi.org/10.1023/B:RUJO.0000045197.43364.1d

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  • DOI: https://doi.org/10.1023/B:RUJO.0000045197.43364.1d

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