Electrochemical triamination of alkynes: controllable synthesis of functionalized indolines and indoles

Electrochemically generated N-radicals are powerful reactive intermediates to construct N-heterocycles. However, these N-centered radicals have never been employed in the trifunctionalization of alkynes. We herein report an unprecedented electrocatalytic triamination of alkynes via N-H cleavage, enabling controllable access to a variety of 2,3-diimino indolines and 2,3-diamino indoles. This sustainable strategy employs 2,2,6,6-tetramethylpiperidinooxy (TEMPO) as the redox catalyst and avoids the undesirable use of terminal oxidants, transition metals, and explosive reagents. Mechanistic investigations suggest that this triamination reaction might proceed via 5-endo-dig cyclization of a N-centered radical and two successive radical couplings with a nitrenium intermediate. Furthermore, this triamination strategy concurrently assembles indole scaffolds and two additional amino substituents from readily available anilines, and therefore rapidly increases molecular complexity allowing further synthetic transformations of the 2,3-diamino indole core.

Automated summary

This article reports an unprecedented electrocatalyic triamination of alkynes via N-H cleavage. Using TEMPO as the catalyst, this reaction allows controllable access to a variety of 2,3-diimino indolines and 2,3-diamino indoles. The reaction avoids the use of terminal oxidants, transition metals, and explosive reagents.