C-4 benzofuranylation of pyrazolones by a metal-free catalyzed indirect heteroarylation strategy. Issue 46 (22nd November 2021)

• Record Type: Journal Article
• Authors: Zhang, Wande; Nawaz, Shah; Huang, Yue; Gong, Wenjing; Wei, Xingfu; Qu, Jingping; Wang, Baomin
• Is Part Of: Organic & biomolecular chemistry. Volume 19:Issue 46(2021)
• Page Start: 10215
• Page End: 10222
• Publication Date: 2021-11-22
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/d1ob01920a
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : A metal-free catalyzed indirect heteroarylation of pyrazolones with 2-(3-hydroxy-3, 3-diarylprop-1-yn-1-yl)phenols has been developed, delivering a wide range of novel 4-benzofuran-substituted pyrazolone derivatives. Abstract : A metal-free catalyzed indirect heteroarylation of pyrazolones with 2-(3-hydroxy-3, 3-diarylprop-1-yn-1-yl) phenols has been developed, and a series of novel 4-benzofuranyl substituted pyrazolone derivatives were obtained in moderate to excellent yields (up to 90%). The process has the salient features of metal-free catalysis, operational simplicity, good substrate compatibility and mild reaction conditions. In particular, the integration of the pyrazolone skeleton and benzofuran scaffold into a single molecule is expected to be of potential interest for medicinal research. In addition, the yield and efficiency are basically maintained in the gram-scale experiment, which makes the practical application of the process more prominent.