Issue 34, 2023

Rhodium(i)-catalyzed cascade C(sp2)–H bond alkylation – amidation of anilines: phosphorus as traceless directing group

Abstract

We introduce a versatile Rh(I)-catalyzed cascade reaction, combining C(sp2)–H bond functionalization and amidation between N-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 ortho-C(sp2)–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.

Graphical abstract: Rhodium(i)-catalyzed cascade C(sp2)–H bond alkylation – amidation of anilines: phosphorus as traceless directing group

Supplementary files

Article information

Article type
Edge Article
Submitted
12 Jun 2023
Accepted
01 Aug 2023
First published
01 Aug 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2023,14, 9055-9062

Rhodium(I)-catalyzed cascade C(sp2)–H bond alkylation – amidation of anilines: phosphorus as traceless directing group

M. Peng, D. Ari, T. Roisnel, H. Doucet and J. Soulé, Chem. Sci., 2023, 14, 9055 DOI: 10.1039/D3SC02992A

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