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Uncatalyzed Addition and Cyclization of TSN3 to 1,1-Enediamines: An Effective Green Route to Highly Functionalized 1,2,3-Triazole Compounds

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Submitted:

19 July 2018

Posted:

19 July 2018

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Abstract
Novel 1,2,3-triazole compounds 3–4 were synthesised via the regioselective addition and cyclization reaction of 1,1-enediamines (EDAMs) 1 with p-methylbenzenesulfonyl azide (TsN3) 2 in 1,4-dioxane at refluxing for 5 hours. As a result, 1,2,3-triazoles 3–4 can be easily and efficiently obtained via catalyst-free click chemistry. The reactions have some advantages such as metal-free catalyst, excellent yield, inexpensive raw materials, and convenient final treatment.
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Subject: Chemistry and Materials Science  -   Organic Chemistry
Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.
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