Towards the Development of a Commercial Process To Produce Muvalaplin. Part I: Preparation of a Key Intermediate by an Evans Auxiliary-Assisted Asymmetric Alkylation

Herein, we describe the development of a large-scale process for an intermediate in the synthesis of muvalaplin, a small-molecule lipoprotein(a) inhibitor for the potential treatment of cardiovascular disease. After initially identifying and exploring different methods for installing the required stereochemistry, we focused on an auxiliary-controlled asymmetric alkylation and developed an early-phase route into a scalable process. Each step was optimized, leading to improvements in safety, robustness, and cost of goods, which ultimately resulted in a 35% yield increase over four steps and a 2× reduction in PMI. The process was safely scaled to >100 kg, thus ensuring clinical supply and laying the foundation for a commercial route.

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Publication Details

Journal
Organic Process Research & Development
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.oprd.6c00010
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
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article

Towards the Development of a Commercial Process To Produce Muvalaplin. Part I: Preparation of a Key Intermediate by an Evans Auxiliary-Assisted Asymmetric Alkylation

Fuliang Wei, Matthew J. Genzink, Srinivas Gangula, Jianfei Dai et al.
Organic Process Research & Development
Cyclopropane Reaction Mechanisms
article

Towards the Development of a Commercial Process To Produce Muvalaplin. Part I: Preparation of a Key Intermediate by an Evans Auxiliary-Assisted Asymmetric Alkylation

Fuliang Wei, Matthew J. Genzink, Srinivas Gangula, Jianfei Dai, Dajiang Jing, Kevin F. McGee, John R. Rizzo, Jayda Yancey, Antonio Navarro, Mai Khanh Hawk, Silong Zhang, Ahren Green
article en

Abstract

Herein, we describe the development of a large-scale process for an intermediate in the synthesis of muvalaplin, a small-molecule lipoprotein(a) inhibitor for the potential treatment of cardiovascular disease. After initially identifying and exploring different methods for installing the required stereochemistry, we focused on an auxiliary-controlled asymmetric alkylation and developed an early-phase route into a scalable process. Each step was optimized, leading to improvements in safety, robustness, and cost of goods, which ultimately resulted in a 35% yield increase over four steps and a 2× reduction in PMI. The process was safely scaled to >100 kg, thus ensuring clinical supply and laying the foundation for a commercial route.

Organic Process Research & DevelopmentVol. 30(4)
Eli Lilly (United States) (US), Tianjin Economic-Technological Development Area (CN)
Openalex Percentile: Top 31%
Cyclopropane Reaction Mechanisms
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