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

The Kizhner Research Center

Research output: Contribution to journal › Article › peer-review

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 language	English
Pages (from-to)	3771-3773
Number of pages	3
Journal	Tetrahedron Letters
Volume	55
Issue number	28
DOIs	https://doi.org/10.1016/j.tetlet.2014.05.052
Publication status	Published - 9 Jul 2014

Keywords

Aminopyridines
Diazotization
Trifluoromethanesulfonic acid

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2014.05.052

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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 journal › Article › peer-review

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AU - Filimonov, Victor D.

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