Rapid α-Amination of N-Substituted Indoles by Using DBU-Activated N-Haloimides as Nitrogen Sources

Abstract

By using the <i>N</i>-haloimide/DBU protocol, the electrophilic imidation at C2-position of N-substituted indoles has been achieved in high efficiency. The dual activation of <i>N</i>-haloimide by DBU to simultaneously achieve a more electrophilic bromine and a more nucleophilic nitrogen atom, is demonstrated to be crucial in this transformation. The process involves tandem bromonium ion formation, electrophilic addition, and elimination of HBr. The protocol provides a novel, efficient, green, and complimentary access to α-imidated indoles under mild conditions, without the necessity of external nitrogen sources.