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The tautomerism of 5-aminotetrazole

VII. Synthesis, structure, and spectra of diacyl derivatives of 5-amino-1-methyltetrazole and 5-amino-2-methyltetrazole

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

In the reaction of 5-amino-1-methyltetrazole and 5-amino-2-methyltetrazole with carboxylic acid anhydrides or chlorides, diacylamides are obtained in addition to monoacyl derivatives. The results of independent synthesis and a study of IR and PMR spectra have shown that in the diacylamides considered both acyl groups are attached to the same (the exocyclic) nitrogen atom.

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Authors and Affiliations

  1. Tyumen Industrial Institute, USSR

    V. P. Shchipanov

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  1. V. P. Shchipanov
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Additional information

For part VI, see [1].

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Shchipanov, V.P. The tautomerism of 5-aminotetrazole. Chem Heterocycl Compd 5, 688–691 (1969). https://doi.org/10.1007/BF00957392

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  • DOI: https://doi.org/10.1007/BF00957392

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