Synthesis
DOI: 10.1055/a-2735-9141
Paper

Facile Synthesis of 1H-Indoliums via Silica Gel-Assisted Silver-Catalyzed Intramolecular Hydroammoniumation of ortho-Alkynylanilines

Authors

  • Mio Matsumura

    1   School of Pharmaceutical Sciences, Aichi Gakuin University, Nagoya, Japan
  • Masato Kawakubo

    1   School of Pharmaceutical Sciences, Aichi Gakuin University, Nagoya, Japan
  • Haruka Ohta

    1   School of Pharmaceutical Sciences, Aichi Gakuin University, Nagoya, Japan
  • Chihiro Kusakabe

    1   School of Pharmaceutical Sciences, Aichi Gakuin University, Nagoya, Japan
  • Yuki Murata

    1   School of Pharmaceutical Sciences, Aichi Gakuin University, Nagoya, Japan
  • Shuji Yasuike

    1   School of Pharmaceutical Sciences, Aichi Gakuin University, Nagoya, Japan

Supported by: Institute of Pharmaceutical Life Sciences, Aichi Gakuin University
Funding Information This research was supported by a research grant from Institute of Pharmaceutical Life Sciences, Aichi Gakuin University.


Graphical Abstract

Abstract

1H-Indoliums, a class of cationic heterocycles, with potential industrial applications have been used as components in capacitors. In this study, we describe a facile method for the synthesis of indoliums using silica gel-assisted silver-catalyzed intramolecular hydroammoniumation of ortho-alkynylanilines. The cyclization of alkynylanilines in the presence of AgOTf (5 mol%), LiOTf (1 equiv.), and SiO2 [SiO2/AgOTf (w/w: 199/1)] in CH2Cl2 at room temperature under aerobic conditions afforded indoliums in good-to-excellent yields. This reaction is an effective and novel method, in which the 5-endo-dig cyclization reaction to obtain indoliums is promoted only by the addition of SiO2 in the presence of a silver catalyst. This novel methodology offers a practical and effective route for the synthesis of indoliums under mild conditions.



Publication History

Received: 23 August 2025

Accepted after revision: 17 October 2025

Article published online:
20 November 2025

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