Ganesan Balaji, Senadi Gopal Chandru, Guo Bing-Chun, Hung Min-Yuan, Lin Wei-Yu
Department of Medicinal and Applied Chemistry, Kaohsiung Medical University No. 100 Shi-chuan, 1st Road Kaohsiung 807 Taiwan
Department of Chemistry, SRM Institute of Science and Technology Kattankulathur Chennai-603203 India.
RSC Adv. 2018 Dec 7;8(71):40968-40973. doi: 10.1039/c8ra09214a. eCollection 2018 Dec 4.
In this paper, a copper(ii)-catalyzed reaction of -alkynylanilines with dimethylformamide (DMF) in the presence of oxygen has been developed for synthesizing multisubstituted 3-formyl indole scaffolds. This one-pot reaction proceeds through a cascade 5--dig cyclization followed by formylation to construct 1,2-disubstituted 3-formyl indoles. The key aspects of this synthesis method are the broad substrate scope (with 38 examples), and well tolerating various functional groups. In addition, a detailed mechanism has been proposed, where DMF may serve as a carbon source for the C3 formylation of the obtained indole derivatives.
本文开发了一种在氧气存在下铜(II)催化的炔基苯胺与二甲基甲酰胺(DMF)反应,用于合成多取代的3-甲酰基吲哚骨架。该一锅法反应通过串联的5-endo-dig环化反应,随后进行甲酰化反应,构建1,2-二取代的3-甲酰基吲哚。这种合成方法的关键之处在于底物范围广泛(有38个实例),并且对各种官能团具有良好的耐受性。此外,还提出了详细的机理,其中DMF可能作为所得吲哚衍生物C3甲酰化的碳源。