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

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2020-09-28 DOI:10.1021/acscombsci.0c00173
Jimin Hwang, Lydia Borgelt, Peng Wu*
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引用次数: 10

Abstract

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.

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多组分Petasis反应合成功能化2-氨基噻吩和噻吩二氮杂类
多组分Petasis反应已被广泛应用于合成功能化胺基块和生物活性化合物。采用非典型反应底物的伯胺有助于扩大Petasis反应的应用范围。本研究以gewald反应衍生的2-氨基噻吩为胺类底物,在温和条件下以六氟-2-丙醇为溶剂,克服了2-氨基噻吩在Petasis反应中的低反应活性。由于存在多个功能手柄,所获得的Petasis产品可以进行进一步的转换。选定的Petasis产品的分子内环化提供取代的三环杂环,其中包含药学上有趣的硫代二氮杂环部分。
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CiteScore
7.20
自引率
4.30%
发文量
567
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