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Synthesis of 2,4-Disubstituted Oxazoles and Thiazoles via Brønsted Acid-Catalyzed Cyclization of α-diazoketones with Amides.
Luo, Mengxiang; Li, Lewan; Chen, Shixin; Yan, Qiongjiao; Lv, Jian; Zeng, Jie; Wang, Haifeng; Gu, Shuangxi; Chen, Fener.
Afiliación
  • Luo M; School of Chemical Engineering & Pharmacy and Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
  • Li L; School of Chemical Engineering & Pharmacy and Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
  • Chen S; School of Chemical Engineering & Pharmacy and Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
  • Yan Q; School of Chemical Engineering & Pharmacy and Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
  • Lv J; School of Chemical Engineering & Pharmacy and Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
  • Zeng J; School of Chemical Engineering & Pharmacy and Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
  • Wang H; School of Chemical Engineering & Pharmacy, Wuhan Institute of Technology, Wuhan 430205, China.
  • Gu S; Jiangxi Province Key Laboratory of Synthetic Chemistry, East China University of Technology, Nanchang 330013, China.
  • Chen F; Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China.
J Org Chem ; 89(7): 5038-5048, 2024 Apr 05.
Article en En | MEDLINE | ID: mdl-38517950
ABSTRACT
A novel method is described for the synthesis of 2,4-disubstituted oxazole and thiazole derivates via the coupling of α-diazoketones with (thio)amides or thioureas using trifluoromethanesulfonic acid (TfOH) as a catalyst. This protocol is characterized by mild reaction conditions, metal-free, and simplicity and also features good functional group tolerance, good to excellent yields, and a broad substrate scope with more than 40 examples. Experimental studies suggest a mechanism involving 2-oxo-2-phenylethyl trifluoromethanesulfonate as the key intermediate.

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China