Electrochemically Enabled Nickel-Catalyzed Intramolecular Amination of Aryl Chlorides with Hydrazones
Herein, we report the electrochemical Ni-catalyzed intramolecular C-N coupling reaction with aryl chlorides, providing a novel catalytic approach for the synthesis of medicinally important indazole scaffold. The method enables challenging C-Cl activation and C=N bond isomerization in hydrazones at room temperature under constant-current electrolysis in an undivided cell. Mechanistic and DFT studies suggest that rapid ligand exchange drives the Ni(I)/Ni(III) catalytic cycle as the primary pathway. The methodology has been successfully applied for the late-stage functionalization and formal synthesis of lificiguat (YC-1), YD-3, and axitinib.
Authors
- Valmik S. Shinde (ORCID: https://orcid.org/0000-0002-2185-9418)
- Sathish Kumar Mudedla (ORCID: https://orcid.org/0000-0003-3173-5993)
- P Yadunandan Yadav
- R S Kant
- Neetu Malya
- Mayur S. Raut
- Bhanu Sharma
Institutions
- Central Drug Research Institute (IN)
- Academy of Scientific and Innovative Research (IN)
Publication Details
- Journal
- Organic Letters
- Published
- 2026-06-18
- DOI
- https://doi.org/10.1021/acs.orglett.6c02259
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00