Advancing Base Metal Catalysis: Development and Execution of a Ni-catalyzed Borylation/Pd-catalyzed Suzuki Telescoped Process

The development and execution of a nickel-catalyzed borylation/palladium-catalyzed Suzuki telescoped process utilizing the inexpensive NiCl2·6H2O precatalyst for the borylation step are reported. The development of the borylation reaction was guided by a preliminary mechanistic investigation to understand the origin of the dehalogenated side product. The borylation stream was telescoped into a Suzuki coupling to form a bis-heteroaryl bond in the pentacyclic core of afimetoran, an antagonist of toll-like receptors 7/8 (TLR 7/8). The optimization of the Suzuki reaction and kilogram-scale demonstration of the telescoped process showcase the viability of utilizing nickel catalysis in the development of scalable routes to clinical APIs.

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Publication Details

Journal
Organic Process Research & Development
Published
2025-02-10
DOI
https://doi.org/10.1021/acs.oprd.4c00498
Citations
3
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
2.81
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article

Advancing Base Metal Catalysis: Development and Execution of a Ni-catalyzed Borylation/Pd-catalyzed Suzuki Telescoped Process

Eric M. Simmons, Matthew V. Joannou, Matthew J. Goldfogel, Steven R. Wisniewski
3 citations
Organic Process Research & Development
Catalytic Cross-Coupling Reactions
2.81
article

Advancing Base Metal Catalysis: Development and Execution of a Ni-catalyzed Borylation/Pd-catalyzed Suzuki Telescoped Process

Eric M. Simmons, Matthew V. Joannou, Matthew J. Goldfogel, Steven R. Wisniewski
article en
3 citations

Abstract

The development and execution of a nickel-catalyzed borylation/palladium-catalyzed Suzuki telescoped process utilizing the inexpensive NiCl2·6H2O precatalyst for the borylation step are reported. The development of the borylation reaction was guided by a preliminary mechanistic investigation to understand the origin of the dehalogenated side product. The borylation stream was telescoped into a Suzuki coupling to form a bis-heteroaryl bond in the pentacyclic core of afimetoran, an antagonist of toll-like receptors 7/8 (TLR 7/8). The optimization of the Suzuki reaction and kilogram-scale demonstration of the telescoped process showcase the viability of utilizing nickel catalysis in the development of scalable routes to clinical APIs.

Organic Process Research & DevelopmentVol. 29(2)
Bristol-Myers Squibb (United States) (US), Université Bourgogne Franche-Comté (FR)
Openalex Percentile: Top 12%
Catalytic Cross-Coupling Reactions
2.81
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