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Russian Chemical Bulletin

, Volume 67, Issue 11, pp 2054–2057 | Cite as

Synthesis of 2-aminochromone-3-carbaldehyde hydrazones from 3-thiocarbamoylchromones and hydrazines

  • D. Yu. Demin
  • G. М. Rodionova
  • V. N. Yarovenko
  • М. М. KrayushkinEmail author
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  • 11 Downloads

Abstract

Reaction of 3-thiocarbamoylchromones with hydrazines is accompanied by recyclization affording 2-aminochromone-3-carbaldehyde hydrazones.

Key words

heterocyclization chromones hydrazines hydrazones thioamides recyclization 

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References

  1. 1.
    R. S. Keri, S. Budagumpi, R. K. Pai, R. G. Balakrishna, Eur. J. Med. Chem., 2014, 78, 340.CrossRefGoogle Scholar
  2. 2.
    A. Gaspar, M. J. Matos, J. Garrido, E. Uriarte, F. Borges, Chem. Rev., 2014, 114, 4960.CrossRefGoogle Scholar
  3. 3.
    M. J. Matos, S. Vazquez-Rodriguez, E. Uriarte, L. Santana, F. Borges, Expert Opin. Ther. Patents, 2015, 25, 1.CrossRefGoogle Scholar
  4. 4.
    O. I. Kobeleva, T. M. Valova, V. A. Barachevsky, I. S. Semenova, K. S. Levchenko, V. N. Yarovenko, M. M. Krayushkin, Opt. Spectrosc., 2013, 114, 401.CrossRefGoogle Scholar
  5. 5.
    I. Y. Martynov, V. A. Barachevsky, A. O. Ayt, O. I. Kobeleva, T. M. Valova, K. S. Levchenko, V. N. Yarovenko, M. M. Kra yushkin, Opt. Mater., 2014, 37, 488.CrossRefGoogle Scholar
  6. 6.
    M. Yu. Kornev, V. Ya. Sosnovskikh, Chem. Heterocycl. Compd. (Engl. Transl.), 2016, 52, 71.CrossRefGoogle Scholar
  7. 7.
    V. Y. Sosnovskikh, V. S. Moshkin, M. I. Kodess, J. Heterocycl. Chem., 2010, 47, 629.Google Scholar
  8. 8.
    M. A. Ibrahim, Tetrahedron, 2009, 65, 7687.CrossRefGoogle Scholar
  9. 9.
    D. Y. Demin, K. A. Myannik, P. A. Ermolich, V. N. Yarovenko, M. M. Krayushkin, Mendeleev Commun., 2018, 5, DOI: 10.1016/j.mencom.2018.09.010.Google Scholar
  10. 10.
    A. M. Tsedilin, A. N. Fakhrutdinov, D. B. Eremin, S. S. Zalesskiy, A. O. Chizhov, N. G. Kolotyrkina, V. P. Ananikov, Mendeleev Commun., 2015, 25, 454.CrossRefGoogle Scholar
  11. 11.
    G. Singh, L. Singh, M. P. S. Ishar, Tetrahedron, 2002, 58, 7883.CrossRefGoogle Scholar
  12. 12.
    S. Maiti, S. K. Panja, C. Bandyopadhyay, Indian J. Chem., 2009, 48B, 1447.Google Scholar

Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • D. Yu. Demin
    • 1
  • G. М. Rodionova
    • 2
  • V. N. Yarovenko
    • 1
  • М. М. Krayushkin
    • 1
    Email author
  1. 1.N. D. Zelinsky Institute of Organic ChemistryRussian Academy of SciencesMoscowRussian Federation
  2. 2.I. M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian FederationMoscowRussian Federation

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