Chemistry of Heterocyclic Compounds

, Volume 48, Issue 8, pp 1228–1234

Reaction of 4,6-Dichloro-5-nitrobenzofuroxan with aromatic amines and nitrogen-containing heterocycles

Authors

    • A. E. Arbuzov Institute of Organic and Physical ChemistryKazan Science Center, Russian Academy of Sciences
  • E. A. Chugunova
    • A. E. Arbuzov Institute of Organic and Physical ChemistryKazan Science Center, Russian Academy of Sciences
  • E. V. Mironova
    • A. E. Arbuzov Institute of Organic and Physical ChemistryKazan Science Center, Russian Academy of Sciences
  • D. B. Krivolapov
    • A. E. Arbuzov Institute of Organic and Physical ChemistryKazan Science Center, Russian Academy of Sciences
  • A. R. Burilov
    • A. E. Arbuzov Institute of Organic and Physical ChemistryKazan Science Center, Russian Academy of Sciences
  • L. M. Yusupova
    • Kazan National Research Technological University
  • M. A. Pudovik
    • A. E. Arbuzov Institute of Organic and Physical ChemistryKazan Science Center, Russian Academy of Sciences
Article

DOI: 10.1007/s10593-012-1126-8

Cite this article as:
Gibadullina, E.M., Chugunova, E.A., Mironova, E.V. et al. Chem Heterocycl Comp (2012) 48: 1228. doi:10.1007/s10593-012-1126-8
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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.

Keywords

Benzofuroxanaminationaromatic ringarylationmonosubstitution

Copyright information

© Springer Science+Business Media New York 2012