Selective N1-Acylation of Indazoles with Acid Anhydrides Using an Electrochemical Approach

An electrochemical synthesis method for the selective N1-acylation of indazoles has been developed. This “anion pool” approach electrochemically reduces indazole molecules generating indazole anions and H2. Acid anhydrides are then introduced to the solution resulting in selective acylation of the N...

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Veröffentlicht in:Organic letters 2019-01, Vol.21 (2), p.457-460
Hauptverfasser: Dissanayake, D. M. M. Mevan, Vannucci, Aaron K
Format: Artikel
Sprache:eng
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Zusammenfassung:An electrochemical synthesis method for the selective N1-acylation of indazoles has been developed. This “anion pool” approach electrochemically reduces indazole molecules generating indazole anions and H2. Acid anhydrides are then introduced to the solution resulting in selective acylation of the N1-position of the indazoles. This procedure can also be applied to the acylation of benzimidazoles and indoles. The reaction can also be performed using a 9 V battery without loss of reaction efficiency.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.8b03683