Highly Enantioselective Chemoenzymatic and Kilogram-Scale Process Development of ( <i>S</i> )-3-Bromo-2-(1-methoxyethyl)pyridine

(S)-3-Bromo-2-(1-methoxyethyl)pyridine 1 is a key intermediate of RMC-6236. In this report, we detail the development and optimization of a highly enantioselective chemoenzymatic and kilogram-scale process for 1. The developed process for intermediate (S)-1-(3-Bromopyridin-2-yl)ethanol 3 was performed on 1 kg scale with a substrate concentration of 70.0 g/L, achieving a yield of 93.0% and an ee value of >99.9%. Subsequently, a simple and effective NaHMDS/CH3I methylation system afforded the title compound 1, in 95.0% yield and with >99.9% ee, achieving 88.4% overall yield from intermediate 1-(3-bromopyridin-2-yl)ethanone 2. This represents a notable increase compared to the early stage process (overall yield 55.5%). This optimized highly efficient and sustainable process was demonstrated during kilogram-scale production of 1.

Authors

Institutions

Publication Details

Journal
Organic Process Research & Development
Published
2026-01-20
DOI
https://doi.org/10.1021/acs.oprd.5c00349
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Highly Enantioselective Chemoenzymatic and Kilogram-Scale Process Development of ( S )-3-Bromo-2-(1-methoxyethyl)pyridine

Fuli Zhang, Hao Chen, Jiawei Tang, Li Zhang et al.
Organic Process Research & Development
Enzyme Catalysis and Immobilization
article

Highly Enantioselective Chemoenzymatic and Kilogram-Scale Process Development of ( S )-3-Bromo-2-(1-methoxyethyl)pyridine

Fuli Zhang, Hao Chen, Jiawei Tang, Li Zhang, Ganlan Li, Shaoxin Chen, Jinnai Liu, Jun Yu
article en

Abstract

(S)-3-Bromo-2-(1-methoxyethyl)pyridine 1 is a key intermediate of RMC-6236. In this report, we detail the development and optimization of a highly enantioselective chemoenzymatic and kilogram-scale process for 1. The developed process for intermediate (S)-1-(3-Bromopyridin-2-yl)ethanol 3 was performed on 1 kg scale with a substrate concentration of 70.0 g/L, achieving a yield of 93.0% and an ee value of >99.9%. Subsequently, a simple and effective NaHMDS/CH3I methylation system afforded the title compound 1, in 95.0% yield and with >99.9% ee, achieving 88.4% overall yield from intermediate 1-(3-bromopyridin-2-yl)ethanone 2. This represents a notable increase compared to the early stage process (overall yield 55.5%). This optimized highly efficient and sustainable process was demonstrated during kilogram-scale production of 1.

Organic Process Research & DevelopmentVol. 30(2)
Shanghai Institute of Pharmaceutical Industry (CN)
Responsible consumption and production
Openalex Percentile: Top 83%
Enzyme Catalysis and Immobilization
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Highly Enantioselective Chemoenzymatic and Kilogram-Scale Process Development of ( <i>S</i> )-3-Bromo-2-(1-methoxyethyl)pyridine — Fuli Zhang, Hao Chen, et al. · Organic Process Research & Development (2026) | TGRS Research Map | TGRS