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Amino- and hydroxymethylation of hydride adducts of 2-hydroxy-3,5-dinitropyridine

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Chemistry of Heterocyclic Compounds Aims and scope

A series of 1,5-dinitro-3,3-diazabicyclo[3.3.1]nonan-2-one derivatives has been synthesized by Mannich condensation of the hydride adduct of 2-hydroxy-3,5-dinitropyridine with formaldehyde and primary amines. The structure of the obtained compounds was proved by NMR spectroscopy.

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Authors and Affiliations

  1. Tula L. N. Tolstoy State Pedagogical University, 125 Lenina Ave., Tula, 300026, Russia

    E. V. Ivanova, I. I. Surova, Yu. M. Atroshchenko & I. V. Shahkeldyan

  2. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilova St., Moscow, 119991, Russia

    I. V. Fedyanin

  3. Tula State University, 92 Lenina Ave., Tula, 300012, Russia

    I. V. Blokhin

Authors
  1. E. V. Ivanova
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  2. I. V. Fedyanin
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  3. I. I. Surova
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  4. I. V. Blokhin
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  5. Yu. M. Atroshchenko
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  6. I. V. Shahkeldyan
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Corresponding author

Correspondence to Yu. M. Atroshchenko.

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 1073-1081, July, 2013.

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Ivanova, E.V., Fedyanin, I.V., Surova, I.I. et al. Amino- and hydroxymethylation of hydride adducts of 2-hydroxy-3,5-dinitropyridine. Chem Heterocycl Comp 49, 1000–1008 (2013). https://doi.org/10.1007/s10593-013-1338-6

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  • DOI: https://doi.org/10.1007/s10593-013-1338-6

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