Phenylfurylthieno[2,3-b]pyridyl-methanes. synthesis and reactions of the furan ring transformation

  • D. Yu. Kosulina
  • V. K. Vasilin
  • T. A. Stroganova
  • E. A. Sbitneva
  • A. V. Butin
  • G. D. KrapivinEmail author

Triarylmethane derivatives with various substituents, phenyl, 5-methyl-2-furyl, and 3-acylamino-thieno[2,3-b]pyrid-2-yl have been obtained for the first time. The behavior of these compounds under protolytic conditions has been studied. It was shown that the character of the protection of the amino group of the thienopyridine fragment affects the type of transformation of the furan ring.


3-amino-2-benzoylthieno[2,3-b]pyridines N-[2-(2,5-dioxo-1-phenylhexyl)thieno[2,3-b]pyrid- 3-yl]benzamides (phenyl)(2-acylaminothieno[2,3-b]pyrid-2-yl)carbinols (phenyl)(5-methylfur-2-yl)-(2-acylaminothieno[2,3-b]pyrid-2-yl)methanes 4-(3-phenyl-1H-pyrrolo[2',3':4,5]thieno[2,3-b]pyrid-2-yl)-butan-2-ones alkylation acylation reduction transformation of the furan ring 


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Copyright information

© Springer Science+Business Media, Inc. 2009

Authors and Affiliations

  • D. Yu. Kosulina
    • 1
  • V. K. Vasilin
    • 1
  • T. A. Stroganova
    • 1
  • E. A. Sbitneva
    • 1
  • A. V. Butin
    • 1
  • G. D. Krapivin
    • 1
    Email author
  1. 1.Kuban State University of TechnologyKrasnodarRussia

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