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探究钯催化交叉偶联反应中差向异构化衰减的起源

Investigating the Origin of Epimerization Attenuation during Pd-Catalyzed Cross-Coupling Reactions.

作者信息

Cai Isabelle, Malig Thomas C, Kurita Kenji L, Derasp Joshua S, Sirois Lauren E, Hein Jason E

机构信息

Department of Chemistry, The University of British Columbia, Vancouver, British Columbia V6T 1Z1, Canada.

Department of Synthetic Molecule Analytical Chemistry, Genentech, Inc., South San Francisco, California 94080, United States.

出版信息

ACS Catal. 2024 Aug 3;14(16):12331-12341. doi: 10.1021/acscatal.4c03401. eCollection 2024 Aug 16.

Abstract

Palladium-catalyzed cross-couplings remain among the most robust methodologies to form carbon-carbon and carbon-heteroatom bonds. In particular, carbon-nitrogen (C-N) couplings (Buchwald-Hartwig aminations) find widespread use in fine chemicals industries. The use of base in these reactions is critical for catalyst activation and proton sequestration. Base selection also plays an important role in process design, as strongly basic conditions can impact sensitive stereocenters and result in erosion of stereochemical purity. Herein we investigate the role of a Pd catalyst in suppressing base-mediated epimerization of a sultam stereocenter during a C-N cross-coupling reaction to access the RORγ inhibitor GDC-0022. Online high-performance liquid chromatography-mass spectrometry (HPLC-MS) was employed to acquire reaction time course profiles and to delineate epimerization behavior, identify decomposition pathways, and monitor Pd-containing species. Our ability to monitor organopalladium complexes in real time by HPLC-MS provided strong evidence that the degree of epimerization was correlated to the Pd speciation in solution. Specifically, Pd(II) complexes were associated with mitigating epimerization of six-membered sultams. Additional studies showed that the suppression of epimerization in the presence of Pd(II) can impact Pd-catalyzed reactions of other substrates such as enolizable ketones, thus providing practical insight on the execution and optimization of such processes.

摘要

钯催化的交叉偶联反应仍然是形成碳-碳键和碳-杂原子键最可靠的方法之一。特别是碳-氮(C-N)偶联反应(布赫瓦尔德-哈特维希胺化反应)在精细化工行业中得到了广泛应用。这些反应中碱的使用对于催化剂活化和质子螯合至关重要。碱的选择在工艺设计中也起着重要作用,因为强碱性条件会影响敏感的立体中心并导致立体化学纯度的降低。在此,我们研究了钯催化剂在C-N交叉偶联反应中抑制环丁砜立体中心的碱介导差向异构化以获得RORγ抑制剂GDC-0022的作用。采用在线高效液相色谱-质谱联用(HPLC-MS)技术获取反应时间进程曲线,描绘差向异构化行为,确定分解途径,并监测含钯物种。我们通过HPLC-MS实时监测有机钯配合物的能力提供了有力证据,表明差向异构化程度与溶液中的钯形态相关。具体而言,Pd(II)配合物与减轻六元环丁砜的差向异构化有关。进一步的研究表明,在Pd(II)存在下抑制差向异构化会影响其他底物(如可烯醇化的酮)的钯催化反应,从而为这类反应的实施和优化提供了实际见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91de/11334108/15b67e6acc90/cs4c03401_0012.jpg

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