A new synthesis of pyridinyl trifluoromethanesulfonates via one-pot diazotization of aminopyridines in the presence of trifluoromethanesulfonic acid

Elena A. Krasnokutskaya, Assiya Zh Kassanova, Makpal T. Estaeva, Victor D. Filimonov

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

The first method for the direct one-pot transformation of aminopyridines into pyridinyl trifluoromethanesulfonates is developed. The procedure involves diazotization of aminopyridines with sodium nitrite in a DMSO paste in the presence of trifluoromethanesulfonic acid.

Original languageEnglish
Pages (from-to)3771-3773
Number of pages3
JournalTetrahedron Letters
Volume55
Issue number28
DOIs
Publication statusPublished - 9 Jul 2014

Fingerprint

Aminopyridines
Sodium Nitrite
Ointments
Dimethyl Sulfoxide
trifluoromethanesulfonic acid

Keywords

  • Aminopyridines
  • Diazotization
  • Trifluoromethanesulfonic acid

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

A new synthesis of pyridinyl trifluoromethanesulfonates via one-pot diazotization of aminopyridines in the presence of trifluoromethanesulfonic acid. / Krasnokutskaya, Elena A.; Kassanova, Assiya Zh; Estaeva, Makpal T.; Filimonov, Victor D.

In: Tetrahedron Letters, Vol. 55, No. 28, 09.07.2014, p. 3771-3773.

Research output: Contribution to journalArticle

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