REACTION OF 4,6-DICHLORO-5-NITROBENZOFUROXAN WITH AROMATIC AMINES AND NITROGEN-CONTAINING HETEROCYCLES

Authors

  • Э. М. Гибадуллина Институт органической и физической химии им. А. Е. Арбузова Казанского научного центра РАН
  • Е. А. Чугунова A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences
  • Е. В. Миронова A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences
  • Д. Б. Криволапов A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences
  • А. Р. Бурилов A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences
  • Л. М. Юсупова Kazan National Research Technological University
  • М. А. Пудовик A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Science Center, Russian Academy of Sciences

DOI:

https://doi.org/10.1007/1021

Keywords:

benzofuroxan, amination, aromatic ring, arylation, monosubstitution

Abstract

4,6-Dichloro-5-nitrobenzofuroxan reacts with aromatic and heterocyclic amines via the chlorine atom at the position 4 of the aromatic ring to give monоsubstitution products. In a similar reaction with piperazine, both amino groups undergo arylation to give a compound containing two benzofuroxan fragments.

Authors: E. M. Gibadullina, E. A. Chugunova, E. V. Mironova, D. B. Krivolapov, A. R. Burilov, L. M. Yusupova, and M. A. Pudovik

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (8), pp 1228-1234

http://link.springer.com/article/10.1007/s10593-012-1126-8

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Published

2013-10-22

Issue

No. 8 (2012)

Section

Original Papers