One-pot synthesis of <i>trans</i> -2,3-diaminoindolines through 2,3-diamination of electrophilic indolines
Despite recent advances in the synthesis of 2,3-diaminoindole derivatives, construction of 2,3-diaminoindolines, whose two amine moieties on each molecule differ from one another has yet to be achieved. In this work, we developed a concise one-pot protocol for differentiated diamination involving reacting a C2,C3-electrophilic indole reagent with amines to access a variety of previously inaccessible 2,3-diaminoindolines. Furthermore, the synthetic utility of this protocol was demonstrated by a successful gram-scale reaction and further transformation of the 2,3-diaminoindolines.
Authors
- Keisuke Tokushige (ORCID: https://orcid.org/0009-0009-6814-3693)
- Takumi Abe (ORCID: https://orcid.org/0000-0003-1729-1097)
- Yuito Kobori (ORCID: https://orcid.org/0009-0008-5839-888X)
Institutions
- Okayama University (JP)
Publication Details
- Journal
- Organic & Biomolecular Chemistry
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5ob00877h
- Primary Topic
- Synthesis and Biological Evaluation
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Japan Science and Technology Corporation