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用于精密 N-三氟烷基苯胺模块化合成的金属光催化三重偶联反应。

Metallaphotocatalytic triple couplings for modular synthesis of elaborate N-trifluoroalkyl anilines.

作者信息

Zhou Ting, Zhang Zhong-Wei, Nie Jing, Kwong Fuk Yee, Ma Jun-An, Cheung Chi Wai

机构信息

Department of Chemistry, Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Frontiers Science Center for Synthetic Biology (Ministry of Education), Tianjin University, Tianjin, 300072, P. R. of China.

State Key Laboratory of Synthetic Chemistry and Department of Chemistry, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, 999077, P. R. of China.

出版信息

Nat Commun. 2024 Nov 15;15(1):9926. doi: 10.1038/s41467-024-53828-8.

Abstract

The integration of trifluoromethyl groups and three-dimensional quaternary carbon moieties into organic molecules has emerged as a prominent strategy in medicinal chemistry to augment drug efficacy. Although trifluoromethyl (hetero)aromatic amines and derivatives are prevalent frameworks in pharmaceuticals, the development of trifluoromethyl-embedded, intricately structured alkyl amine scaffolds for medicinal research remains a significant challenge. Herein, we present a metallaphotoredox multicomponent amination strategy employing 3,3,3-trifluoropropene, nitroarenes, tertiary alkylamines, and carboxylic acids. This synthetic pathway offers notable advantages, including the accessibility and cost-effectiveness of starting materials, high levels of chemo- and regioselectivity, and modularity. Furthermore, this approach enables the synthesis of a broad spectrum of aniline compounds featuring both trifluoromethyl group and distal quaternary carbon motifs along the aliphatic chains. The accelerated access to such elaborate N-trifluoroalkyl anilines likely involves three sequential radical-mediated coupling events, providing insightful implications for the retrosynthesis of potential compounds in organic synthesis and drug discovery.

摘要

将三氟甲基基团和三维季碳部分引入有机分子已成为药物化学中提高药物疗效的一种重要策略。尽管三氟甲基(杂)芳族胺及其衍生物是药物中普遍存在的骨架,但开发用于药物研究的嵌入三氟甲基的、结构复杂的烷基胺支架仍然是一项重大挑战。在此,我们提出了一种金属光氧化还原多组分胺化策略,该策略使用3,3,3-三氟丙烯、硝基芳烃、叔烷基胺和羧酸。这种合成途径具有显著优势,包括起始原料的可及性和成本效益、高度的化学和区域选择性以及模块化。此外,这种方法能够合成一系列苯胺化合物,这些化合物在脂肪链上同时具有三氟甲基基团和远端季碳基序。快速获得此类复杂的N-三氟烷基苯胺可能涉及三个连续的自由基介导的偶联事件,这为有机合成和药物发现中潜在化合物的逆合成提供了有深刻见解的启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fddd/11568185/ea295427f6bb/41467_2024_53828_Fig1_HTML.jpg

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