Heptafluorobutyric Acid-Induced Cross-Dehydrogenative Coupling Reactions of 1,2,4-Triazines. Part 2: p-Coupling with Arylamines

Abstract A heptafluorobutyric acid-induced cross-dehydrogenative coupling reaction of arylamines with 1,2,4-triazines has been described. This metal-free protocol enables regioselective para-C–H hetarylation of diverse arylamines including well-known fluorophore scaffolds, such as triphenylamine, carbazole, and phenothiazine, with easily accessible 1,2,4-triazines under mild conditions. This approach has potential for drug development and material design.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-09-21
DOI
https://doi.org/10.1021/acs.joc.6c00932
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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Heptafluorobutyric Acid-Induced Cross-Dehydrogenative Coupling Reactions of 1,2,4-Triazines. Part 2: p-Coupling with Arylamines

Dmitry S. Kopchuk, Ainur D. Sharapov, Igor А. Khalymbadzha, Anton N. Tsmokalyuk et al.
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
article

Heptafluorobutyric Acid-Induced Cross-Dehydrogenative Coupling Reactions of 1,2,4-Triazines. Part 2: p-Coupling with Arylamines

Dmitry S. Kopchuk, Ainur D. Sharapov, Igor А. Khalymbadzha, Anton N. Tsmokalyuk, Ramil F. Fatykhov, Elisaveta M. Gurina, Alexander S. Novikov, Anastasia P. Potapova, Vasiliy S. Gaviko
article en

Abstract

Abstract A heptafluorobutyric acid-induced cross-dehydrogenative coupling reaction of arylamines with 1,2,4-triazines has been described. This metal-free protocol enables regioselective para-C–H hetarylation of diverse arylamines including well-known fluorophore scaffolds, such as triphenylamine, carbazole, and phenothiazine, with easily accessible 1,2,4-triazines under mild conditions. This approach has potential for drug development and material design.

The Journal of Organic Chemistry
National Research University Higher School of Economics (RU), Ural Federal University (RU), Immanuel Kant Baltic Federal University (RU), Sirius University of Science and Technology (RU), M.N. Mikheev Institute of Metal Physics (RU)
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Openalex Percentile: Top 20%
Catalytic C–H Functionalization Methods
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