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Chemistry of Heterocyclic Compounds

, Volume 52, Issue 1, pp 45–51 | Cite as

Synthesis of N-alkylated benzo- and pyridothienopyrrolo-[1,2a][1,4]diazepin-6-ones acting as antidotes against the herbicide 2,4-D

  • Tat’yana A. Stroganova
  • Vladimir K. Vasilin
  • Gennady D. Krapivin
  • Vladimir D. Strelkov
  • Ludmila V. Dyadyuchenko
Article

We report N-alkylation reactions of pyrrolo[1,2-a][1,4]diazepin-6-ones annulated with a benzene ring or thieno[2,3-b]pyridine system. A range of new N5-substituted pyrrolodiazepines were synthesized, including compounds acting as antidotes against the herbicide 2,4-D.

Keywords

annulated pyrrolo[1,2-a][1,4]diazepinones N-alkylation antidotes biological activity herbicide 2,4-D 

Notes

This work was carried out within the framework of the Federal targeted program " Research and Development in the Priority Areas of Development of the Russian Scientific and Technological Complex for years 2014–2020". The identification code of applied scientific research (project) is RFMEF157714X0046.

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Copyright information

© Springer Science+Business Media New York 2016

Authors and Affiliations

  • Tat’yana A. Stroganova
    • 1
  • Vladimir K. Vasilin
    • 1
  • Gennady D. Krapivin
    • 1
  • Vladimir D. Strelkov
    • 2
  • Ludmila V. Dyadyuchenko
    • 3
  1. 1.Kuban State Technological UniversityKrasnodarRussia
  2. 2.Kuban State UniversityKrasnodarRussia
  3. 3.All-Russian Scientific Research Institute of Biological Plant ProtectionRussian Academy of Agricultural SciencesKrasnodarRussia

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