Springer Nature is making SARS-CoV-2 and COVID-19 research free. View research | View latest news | Sign up for updates

The aminomethylation of 2-nitro-3-hydroxpyridine


  1. 1.

    The aminomethylation of 2-nitro-3-hydroxypyridine has been studied.

  2. 2.

    On aminomethylation 2-nitro-3-hydroxypyridine forms 6-monosubstituted Mannich bases.

This is a preview of subscription content, log in to check access.

Literature cited

  1. 1.

    H. Hellmann and G. Opitz,α-Aminoalkylierung, Verlag Chemie (1960).

  2. 2.

    L. D. Smirnov, V. P. Lezina, V. F. Bystrov, and K. M. Dyumaev, Izv. AN SSSR, Ser. Khim.,1965, 198.

  3. 3.

    K. M. Dyumaev, L. D. Smirnov, and V. F. Bystrov, Izv. AN SSSR, Otd. khim. n.,1962, 883; L. D. Smirnov, S. L. Or lova, V. P. Lezina, and K. M. Dyumaev, Izv. AN SSSR, Ser. Khim.1967, 1816. 2611

Download references

Author information

Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2742–2744, December, 1967.

The authors are grateful to N. M. Émanuel for his continuous interest in the work.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Smirnov, L.D., Kartasheva, T.P., Lezina, V.P. et al. The aminomethylation of 2-nitro-3-hydroxpyridine. Russ Chem Bull 16, 2609–2611 (1967).

Download citation


  • Mannich Base