Synlett 2025; 36(20): 3368-3372
DOI: 10.1055/a-2675-4185
Letter

Synthesis of 2-Arylquinoxalines from Sulfoxonium Ylides in the Absence of Sacrificial Electrophile and Base

Autoren

  • Khanh T. N. Ong

    VNU-HCM Key Laboratory for Advanced Materials and Structures, Vietnam National University Ho Chi Minh City Ho Chi Minh City University of Technology, Ho Chi Minh City, Viet Nam (Ringgold ID: RIN117295)
  • Khanh T. M. Le

    VNU-HCM Key Laboratory for Advanced Materials and Structures, Vietnam National University Ho Chi Minh City Ho Chi Minh City University of Technology, Ho Chi Minh City, Viet Nam (Ringgold ID: RIN117295)
  • Anh T. Nguyen

    VNU-HCM Key Laboratory for Advanced Materials and Structures, Vietnam National University Ho Chi Minh City Ho Chi Minh City University of Technology, Ho Chi Minh City, Viet Nam (Ringgold ID: RIN117295)
  • Tung T. Nguyen

    VNU-HCM Key Laboratory for Advanced Materials and Structures, Vietnam National University Ho Chi Minh City Ho Chi Minh City University of Technology, Ho Chi Minh City, Viet Nam (Ringgold ID: RIN117295)


Graphical Abstract

Abstract

We report a method for the annulation of 1,2-phenylenediamines and aryl sulfoxonium ylides to yield 2-arylquinoxalines. Known conditions often require sacrificial electrophiles, an oxidative solvent (i.e., DMSO), and an overstoichiometric amount of base. Herein, conditions including the use of the catalytic amount of Bu4NI and m-xylene solvent to facilitate the formation of 2-arylquinoxalines in good to excellent yields have been developed. Functionalities including halogens, protected phenol, and secondary amine groups were tolerant.



Publikationsverlauf

Eingereicht: 02. Juni 2025

Angenommen nach Revision: 03. August 2025

Accepted Manuscript online:
04. August 2025

Artikel online veröffentlicht:
26. August 2025

© 2025. Thieme. All rights reserved.

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany