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Synthesis and regioselective cycloaddition reaction of 2,4,6-triazido-3-chloro-5-cyanopyridine with norbornene

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Treatment of 3-cyanotetrachloropyridine with sodium azide gives 2,4,6-triazido-3-chloro-5-cyanopyridine. This compound reacts regioselectively with norbomene to form an aziridinyl cydoadduct only at the azido group in position 4 of the pyridine ring.

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References

  1. E. F. V. Scriven and K. Turnbull, Chem. Rev., 88, 297 (1988).

    Google Scholar 

  2. C. E. Pannell, U. S. Patent 3883542, Russ. Zh. Khim., 5H372 (1976).

  3. R. M. Claramunt, J. Elguero, R. Faure, and J. P. Galy, Ann. Quim., C82, 61 (1986).

    Google Scholar 

  4. G. L'Abbe, Chem. Rev., 69, 345 (1969).

    Google Scholar 

  5. I. R. A. Barnard, G. E. Chivers, R. J. W. Cremlyn, and K. G. Mootoosamy, Austral. J. Chem., 27, 171 (1974).

    Google Scholar 

  6. H. Suschitzky, W. Kramer, R. Neidlen, P. Rosyk, and T. Bonn, J. Chem. Soc. Perkin 1, No. 4, 923 (1991).

    Google Scholar 

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1650–1652, December, 1993.

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Chapyshev, S.V. Synthesis and regioselective cycloaddition reaction of 2,4,6-triazido-3-chloro-5-cyanopyridine with norbornene. Chem Heterocycl Compd 29, 1426–1427 (1993). https://doi.org/10.1007/BF00531405

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  • DOI: https://doi.org/10.1007/BF00531405

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