Russian Journal of Organic Chemistry

, Volume 53, Issue 10, pp 1573–1577 | Cite as

New functionalized amino derivatives of 2-hydroxyphenyl-1,3,5-triazines

  • E. Yu. Shasheva
  • N. I. Vikrishchuk
  • L. D. Popov
  • S. A. Borodkin


4-(2-Hydroxyphenyl)-1,3,5-triazin-2-ylcyanamides reacted with sodium azide to give N-(tetrazol-5-yl)-1,3,5-triazin-2-amines, and their reaction with allyl bromide afforded allyl(1,3,5-triazin-2-yl)cyanamides. Acetylation of 4-(2-hydroxyphenyl)-1,3,5-triazin-2-amines involved only the amino group with formation of diacetylamino derivatives, whereas the phenolic hydroxy group remained intact. The reaction of triazinamines with 2,5-dimethoxytetrahydrofuran in the presence of P2O5 gave pyrrolyl-substituted triazines.


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Copyright information

© Pleiades Publishing, Ltd. 2017

Authors and Affiliations

  • E. Yu. Shasheva
    • 1
  • N. I. Vikrishchuk
    • 1
  • L. D. Popov
    • 1
  • S. A. Borodkin
    • 1
  1. 1.Southern Federal UniversityRostov-on-DonRussia

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