Synthesis of <i>N</i><sup>2</sup>-Substituted 1,2,3-Triazoles

We present a novel synthetic approach for the synthesis of the 1,2,3-triazole core, with a particular focus on the direct and regioselective synthesis of the synthetically more challenging triazoles having additional substituents at the N2 nitrogen atom. Through treatment of readily accessible geminal diazides with organic hydrazines under mild thermolysis conditions, a broad spectrum of N2-alkyl- and N2-aryl-1,2,3-triazoles are easily generated. For example, geminal diazides derived from ketoesters, ketoamides, and ketones were converted under the reaction conditions. The product structures were confirmed via NMR as well as single-crystal structure analysis.

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Publication Details

Journal
Organic Letters
Published
2024-10-08
DOI
https://doi.org/10.1021/acs.orglett.4c03204
Citations
3
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.75
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article

Synthesis of N2-Substituted 1,2,3-Triazoles

Philipp Klahn, Hülya Aldemir, Fabian Mohr, Stefan F. Kirsch et al.
3 citations
Organic Letters
Click Chemistry and Applications
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article

Synthesis of N2-Substituted 1,2,3-Triazoles

Philipp Klahn, Hülya Aldemir, Fabian Mohr, Stefan F. Kirsch, Kevin A. Kunz, Bastian L. Springer
article en
3 citations

Abstract

We present a novel synthetic approach for the synthesis of the 1,2,3-triazole core, with a particular focus on the direct and regioselective synthesis of the synthetically more challenging triazoles having additional substituents at the N2 nitrogen atom. Through treatment of readily accessible geminal diazides with organic hydrazines under mild thermolysis conditions, a broad spectrum of N2-alkyl- and N2-aryl-1,2,3-triazoles are easily generated. For example, geminal diazides derived from ketoesters, ketoamides, and ketones were converted under the reaction conditions. The product structures were confirmed via NMR as well as single-crystal structure analysis.

Organic LettersVol. 26(41)
University of Wuppertal (DE)
Openalex Percentile: Top 32%
Click Chemistry and Applications
0.75
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