AMINO- AND HYDROXYMETHYLATION OF HYDRIDE ADDUCTS OF 2-HYDROXY-3,5-DINITROPYRIDINE

Authors

  • Е. В. Иванова Tula L. N. Tolstoy State Pedagogical University
  • И. В. Федянин A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
  • И. И. Сурова Tula L. N. Tolstoy State Pedagogical University
  • И. В. Блохин Tula State University
  • Ю. М. Атрощенко Tula L. N. Tolstoy State Pedagogical University
  • И. В. Шахкельдян Tula L. N. Tolstoy State Pedagogical University

DOI:

https://doi.org/10.1007/784

Keywords:

3, 7-diazabicyclo[3.3.1]nonanes, 2-hydroxy-3, 5-dinitropyridine, Mannich reaction

Abstract

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.

Authors: E. V. Ivanova, I. V. Fedyanin, I. I. Surova, I. V. Blokhin, Yu. M. Atroshchenko, and I. V. Shahkeldyan.

English Translation in Chemistry of Heterocyclic Compounds, 2013, 49 (7), pp 1000-1008

http://link.springer.com/article/10.1007/s10593-013-1338-6

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Published

2013-07-02

Issue

No. 7 (2013)

Section

Original Papers