Peng Marie, Ari Denis, Roisnel Thierry, Doucet Henri, Soulé Jean-François
Univ. Rennes, CNRS UMR6226 Rennes F-3500 France.
Chimie ParisTech, PSL University, CNRS, Institute of Chemistry for Life and Health Sciences 75005 Paris France
Chem Sci. 2023 Aug 1;14(34):9055-9062. doi: 10.1039/d3sc02992a. eCollection 2023 Aug 30.
We introduce a versatile Rh(i)-catalyzed cascade reaction, combining C(sp)-H bond functionalization and amidation between -arylphosphanamines and acrylates. This innovative approach enables the rapid synthesis of dihydroquinolinone scaffolds, a common heterocycle found in various pharmaceuticals. Notably, the presence of the phosphorus atom facilitates the aniline -C(sp)-H bond activation prior to N-P bond hydrolysis, streamlining one-pot intramolecular amidation. Moreover, we demonstrate the applicability of this reaction by synthesizing an antipsychotic drug. Detailed mechanistic investigations revealed the involvement of a Rh-H intermediate, with substrate inhibition through catalyst saturation.
我们介绍了一种通用的铑(I)催化的串联反应,该反应结合了C(sp)-H键官能化以及-芳基膦胺与丙烯酸酯之间的酰胺化反应。这种创新方法能够快速合成二氢喹啉酮骨架,这是一种在各种药物中常见的杂环。值得注意的是,磷原子的存在促进了在N-P键水解之前苯胺-C(sp)-H键的活化,简化了一锅法分子内酰胺化反应。此外,我们通过合成一种抗精神病药物证明了该反应的适用性。详细的机理研究表明涉及铑-氢中间体,并且通过催化剂饱和存在底物抑制作用。