Chemical Genomics Centre and Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund 44227, Germany.
ACS Comb Sci. 2020 Oct 12;22(10):495-499. doi: 10.1021/acscombsci.0c00173. Epub 2020 Sep 28.
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.
多组分 Petasis 反应已广泛应用于功能化胺砌块和生物活性化合物的合成。使用不是典型反应性底物的一级芳基胺有助于扩大 Petasis 反应的应用范围。在本研究中,我们展示了使用 Gewald 反应衍生的 2-氨基噻吩作为胺底物合成功能化 2-氨基噻吩,通过在温和条件下使用六氟-2-丙醇作为溶剂克服了它们在 Petasis 反应中的低反应性。由于存在多个功能手性,所得到的 Petasis 产物适合进一步转化。选择的 Petasis 产物的后续分子内环化提供了包含具有药物应用价值的噻吩并二氮杂䓬部分的取代三环杂环。