Medicinal Chemistry, Department of Pharmacy & Pharmacology, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
Department of Chemistry, University of Bath, Claverton Down, Bath, BA2 7AY, UK.
ChemistryOpen. 2020 Nov 5;9(11):1113-1122. doi: 10.1002/open.202000247. eCollection 2020 Nov.
A microwave-based methodology facilitates reaction of 2-aminophenylketones with cyclic ketones to form a quinoline scaffold. Syntheses of amido- and amino-linked 17β-hydroxysteroid dehydrogenase type 3 inhibitors with a benzophenone-linked motif were pursued using 2-aminobenzophenone as building block. Two amido-linked targets were achieved in modest yield, but when using microwave-assisted reductive amination for the amino-linked counterparts an unexpected product was observed. X-ray crystallography revealed it as a quinoline derivative, leading to optimisation of a simple and efficient modification of Friedländer methodology. Using reagents and acetic acid catalyst in organic solvent the unassisted reaction proceeds only over several days and in very poor yield. However, by employing neat acetic acid as both solvent and acid catalyst with microwave irradiation at 160 °C quinoline synthesis is achieved in 5 minutes in excellent yield. This has advantages over the previously reported high temperatures or strong acids required, not least given the green credentials of acetic acid, and examples using diverse ketones illustrate applicability. Additionally, he unassisted reaction proceeds effectively at room temperature, albeit much more slowly.
一种基于微波的方法促进了 2-氨基苯甲酮与环酮的反应,形成了喹啉骨架。使用 2-氨基二苯甲酮作为构建块,进行了酰胺基和氨基连接的 17β-羟甾脱氢酶 3 抑制剂的合成。采用微波辅助还原胺化法合成氨基连接的目标化合物时,得到了一个意想不到的产物。X 射线晶体学表明它是一种喹啉衍生物,这导致了对 Friedländer 方法的简单有效的改进。在有机溶剂中使用试剂和乙酸催化剂,未辅助的反应仅在几天内进行,并且产率非常低。然而,通过在 160°C 下使用微波辐射,将纯乙酸用作溶剂和酸催化剂,喹啉的合成在 5 分钟内以优异的产率完成。与之前报道的需要高温或强酸相比,这具有优势,尤其是考虑到乙酸的绿色信誉,并且使用各种酮的例子说明了其适用性。此外,尽管反应速度较慢,但未辅助的反应在室温下也能有效进行。