Multicomponent Petasis Reaction for the Synthesis of Functionalized 2-Aminothiophenes and Thienodiazepines

被引:14
|
作者
Hwang, Jimin [1 ,2 ]
Borgelt, Lydia [1 ,2 ]
Wu, Peng [1 ,2 ]
机构
[1] Max Planck Inst Mol Physiol, Chem Genom Ctr, D-44227 Dortmund, Germany
[2] Max Planck Inst Mol Physiol, Dept Biol Chem, D-44227 Dortmund, Germany
关键词
multicomponent reaction; Petasis reaction; 2-aminothiophenes; thienodiazepines; small molecules; MANNICH REACTION; INHIBITORS; SCAFFOLD; DESIGN;
D O I
10.1021/acscombsci.0c00173
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Multicomponent Petasis reaction has been widely applied for the synthesis of functionalized amine building blocks and biologically active compounds. Employing primary aromatic amines that are not typical reactive substrates contributes to expand the application scope of the Petasis reaction. In this study, we demonstrated the synthesis of functionalized 2-aminothiophenes using Gewald-reaction-derived 2-aminothiophenes as the amine substrates, whose low reactivity in the Petasis reaction was overcome using hexafluoro-2-propanol as the solvent in a mild condition. The obtained Petasis products are amenable for further transformations owing to the presence of multiple functional handles. A following intramolecular cyclization of selected Petasis products afforded substituted tricyclic heterocycles that incorporate a pharmaceutically interesting thienodiazepine moiety.
引用
收藏
页码:495 / 499
页数:5
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