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Cu(I)-Catalyzed Three-Component Annulation for the Synthesis of 3-Acyl Imidazo[1, 5-a]Pyridines from 2-Pyridinyl-Substituted p-Quinone Methides, Terminal Alkynes, and TsN3 Using O2 as the Oxygen Source.
Chen, Yan; Zhang, Chuanhao; Wang, Kunpeng; Li, Mengfan; Tang, Hao; Cheng, Wen; Yin, Jun; Yi, Weiyin.
Afiliação
  • Chen Y; School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China.
  • Zhang C; School of Pharmacy, East China University of Science and Technology, Shanghai 200237, P. R. China.
  • Wang K; School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China.
  • Li M; School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China.
  • Tang H; School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China.
  • Cheng W; School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China.
  • Yin J; Shanghai No.4 Reagent Chemical Co., Ltd., Shanghai 201512, P. R. China.
  • Yi W; School of Perfume and Aroma Technology, Shanghai Institute of Technology, Shanghai 201418, P. R. China.
J Org Chem ; 89(8): 5423-5433, 2024 Apr 19.
Article em En | MEDLINE | ID: mdl-38557074
ABSTRACT
Currently, most conventional methods to achieve imidazo[1,5-a]pyridines have limitations for the synthesis of 3-acyl imidazo[1,5-a]pyridines. Herein, a novel and efficient Cu(I)-catalyzed three-component annulation method for the synthesis of valuable 3-acyl imidazo[1,5-a]pyridines by the reaction of 2-pyridinyl-substituted p-QMs, terminal alkynes, and TsN3 in the presence of O2 under mild conditions have successfully been developed. The investigation indicated that molecular oxygen (O2) and TsN3, respectively, serving as oxygen and nitrogen sources, were essential for the successful completion of the reaction system.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article