Lenko Illia, Mamontov Alexander, Alayrac Carole, Witulski Bernhard
Laboratoire de Chimie Moléculaire et Thio-organique (LCMT), CNRS UMR 6507, ENSICAEN, Université de Caen, Normandie Univ, 6 Bd Maréchal Juin, 14050 Caen, France.
Molecules. 2024 Jul 26;29(15):3505. doi: 10.3390/molecules29153505.
A novel synthesis strategy to access 2-alkoxyquinoline derivatives via a palladium-driven cascade reaction is disclosed. Unlike classic methods based on the alkylation of 2-quinolones with alkyl halides, the present method benefits from the de novo assembly of the quinoline core starting from 1,3-butadiynamides. Palladium-catalyzed reaction cascades with -(2-iodophenyl)--tosyl-1,3-butadiynamides and primary alcohols as external nucleophiles proceed under mild reaction conditions and selectively deliver a variety of differently functionalized 4-alkenyl 2-alkoxyquinolines in a single batch transformation.
公开了一种通过钯驱动的级联反应制备2-烷氧基喹啉衍生物的新型合成策略。与基于2-喹诺酮与卤代烷烃烷基化的经典方法不同,本方法受益于从1,3-丁二炔酰胺开始的喹啉核心的从头组装。钯催化的反应级联反应,以-(2-碘苯基)--甲苯磺酰基-1,3-丁二炔酰胺和伯醇作为外部亲核试剂,在温和的反应条件下进行,并在单批次转化中选择性地提供各种不同功能化的4-烯基2-烷氧基喹啉。