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NitropyridineS. 9*. Synthesis of substituted 3-amino-5-nitropyridines

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Chemistry of Heterocyclic Compounds Aims and scope

Substituted 3-amino-5-nitropyridines have been synthesized by the Curtius, Schmidt, and Hofmann reactions.

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References

  1. G. P. Sagitullina, A. K. Garkushenko, L. V. Glizdinskaya, N. V. Poendaev, D. E. Eremeeva, and R. S. Sagitullin, Khim. Geterotsikl. Soed., 699 (2010). [Chem. Heterocycl. Comp., 46, 553 (2010)].

    Google Scholar 

  2. G. Mosher, in: R. Elderfield (editor), Heterocyclic Compounds [Russian translation], Izd-vo Inostr. Lit., Moscow, 1953, Vol. 1, p 432.

    Google Scholar 

  3. V. L. Rusinov, and O. N. Chupakhin, Nitroazines [in Russian], Nauka, Novosibirsk, 1991, p. 10.

    Google Scholar 

  4. E. Plazek and L. Kuczynski, Zesz. Nauk. Politechn. wrocl., 4, 17 (1954).

    Google Scholar 

  5. M. Kimura and Y. Takano, J. Pharm. Soc. Jpn., 79, 549 (1959).

    CAS  Google Scholar 

  6. M. Nakadate, Y. Takano, T. Hirayama, S. Sakaizawa, T. Hirano, K. Okamoto, K. Hirao, T. Kawamura, and M. Kimura, Chem. Pharm, Bull., 13, 113 (1965).

    CAS  Google Scholar 

  7. P. Tomasik and E. Plazek, Rozn. Chem., 38, 709 (1964).

    CAS  Google Scholar 

  8. F. A. French and E. J. Blanz, J. Med. Chem., 17, 172 (1974).

    Article  CAS  Google Scholar 

  9. P. Tomasik and W. Grzeniek, Rozn. Chem., 43, 569 (1969).

    CAS  Google Scholar 

  10. G. P. Sagitullina, A. K. Garkushenko, E. G. Atavin, and R. S. Sagitullin, Mendeleev Commun., 19, 155 (2009).

    Article  CAS  Google Scholar 

  11. G. P. Sagitullina, A. K. Garkushenko, and R. S. Sagitullin, Khim. Geterotsikl. Soed., 1430 (2009). [Chem. Heterocycl. Comp., 45, 1147 (2009)].

    Google Scholar 

  12. E. S. Willis and D. F. Len, Organic Reactions [Russian translation], Izd-vo Inostr. Lit., Moscow, 1951, Vol. 3, p. 255.

    Google Scholar 

  13. P. Radlick and L. R. Brown, Synthesis, 290 (1974).

  14. B. K. Swaminathan and N. Venkatasubramanian, J. Chem. Soc., Perkin Trans 2, 1161 (1975).

    Google Scholar 

  15. A. S. Radhakrishna, M. E. Parham, R. M. Riggs, and G. M. Loudon, J. Org. Chem., 44, 1746 (1979).

    Article  CAS  Google Scholar 

  16. X. Huang. M. Seid, and J. W. Keillor, J. Org. Chem., 62, 7495 (1997).

    Article  CAS  Google Scholar 

  17. H. Togo, T. Nabana, and K. Yamaguchi, J. Org. Chem., 65, 8391 (2000).

    Article  CAS  Google Scholar 

  18. C. Yu, Y. Jiang, B. Liu, and L. Hu, Tetrahedron Lett., 42, 1449 (2001).

    Article  CAS  Google Scholar 

  19. M. Jure and I. Jaunzeme, Latv. J. Chem., No. 4, 3 (2000).

  20. T. Shioiri, K. Ninomiya, and S. Yamada, J. Am. Chem. Soc., 94, 6203 (1972).

    Article  CAS  Google Scholar 

  21. S. Yamada, Y. Kasai, T. Shioiri, Tetrahedron. Lett., 14, 1595 (1973).

    Article  Google Scholar 

  22. K. Ninomiya, T. Shioiri, and S. Yamada, Tetrahedron, 30, 2151 (1974).

    Article  CAS  Google Scholar 

  23. J. R. Damewood, Jr., P. D. Edwards, S. Feeney, B. C. Gomes, G. B. Steelman, P. A. Tuthill, J. C. Williams, P. Warner, S. A. Woolson, D. J. Wolanin, and C. A. Veale, J. Med. Chem., 37, 3303 (1994).

    Article  CAS  Google Scholar 

  24. G. C. G. Pais and M. E. Maier, J. Org. Chem., 64, 4551 (1999).

    Article  CAS  Google Scholar 

  25. M. T. Migawa and E. E. Swayze, Org. Lett., 2, 3309 (2000).

    Article  CAS  Google Scholar 

  26. G. P. Sagitullina, L. V. Glyzdinskaya, G. V. Sitnikova, and R. S. Sagitullin, Khim. Geterotsikl. Soed., 1518 (2002). [Chem. Heterocycl. Comp., 38, 1336 (2002)].

    Google Scholar 

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Correspondence to G. P. Sagitullina.

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* For Communication 8, see [1].

** Deceased.

Translated from Khimya Geterotsiklicheskikh Soedinenii, No. 10, 1551-1558, October, 2010.

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Sagitullina, G.P., Garkushenko, A.K., Glyzdinskaya, L.V. et al. NitropyridineS. 9*. Synthesis of substituted 3-amino-5-nitropyridines. Chem Heterocycl Comp 46, 1255–1261 (2011). https://doi.org/10.1007/s10593-011-0660-0

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  • DOI: https://doi.org/10.1007/s10593-011-0660-0

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