Process Development of the Novel LpxC Inhibitor T-1228. Part 3: Optimization of the Deprotection Reaction and the Crystallization for the Final Step of API Synthesis

The novel LpxC inhibitor T-1228 is a candidate drug molecule for multidrug-resistant Gram-negative bacterial infection. We developed a process chemistry route to T-1228. The final step of T-1228 drug substance synthesis consists of a deprotection reaction under acidic conditions and a crystallization process incorporating polymorph control. The process parameters of the deprotection reaction were optimized through a Design of Experiments (DoE) study to limit the formation of a critical impurity. The production method established for the crystallization process was developed by means of process analytical technology (PAT): it controls the quality and particle size of the drug substance and selectively yields only the desired crystal polymorph. By applying the newly developed process chemistry route, we have successfully manufactured T-1228 at 24% total yield from commercially available 1,3-diethyl 2-bromo-2-methylpropanedioate.

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Journal
Organic Process Research & Development
Published
2025-11-05
DOI
https://doi.org/10.1021/acs.oprd.5c00167
Primary Topic
Enzyme Structure and Function
Type
article
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article

Process Development of the Novel LpxC Inhibitor T-1228. Part 3: Optimization of the Deprotection Reaction and the Crystallization for the Final Step of API Synthesis

Muneo Shoji, Yuko Suzumura, Yasuhiro Nagato, Noriyuki Nakajima et al.
Organic Process Research & Development
Enzyme Structure and Function
article

Process Development of the Novel LpxC Inhibitor T-1228. Part 3: Optimization of the Deprotection Reaction and the Crystallization for the Final Step of API Synthesis

Muneo Shoji, Yuko Suzumura, Yasuhiro Nagato, Noriyuki Nakajima, Yasutaka Baba
article en

Abstract

The novel LpxC inhibitor T-1228 is a candidate drug molecule for multidrug-resistant Gram-negative bacterial infection. We developed a process chemistry route to T-1228. The final step of T-1228 drug substance synthesis consists of a deprotection reaction under acidic conditions and a crystallization process incorporating polymorph control. The process parameters of the deprotection reaction were optimized through a Design of Experiments (DoE) study to limit the formation of a critical impurity. The production method established for the crystallization process was developed by means of process analytical technology (PAT): it controls the quality and particle size of the drug substance and selectively yields only the desired crystal polymorph. By applying the newly developed process chemistry route, we have successfully manufactured T-1228 at 24% total yield from commercially available 1,3-diethyl 2-bromo-2-methylpropanedioate.

Organic Process Research & DevelopmentVol. 29(12)
Toyama College (JP), Fujifilm (Japan) (JP), Fuji Chemical Industries (Japan) (JP), Toyama Prefectural University (JP)
Openalex Percentile: Top 74%
Enzyme Structure and Function
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Process Development of the Novel LpxC Inhibitor T-1228. Part 3: Optimization of the Deprotection Reaction and the Crystallization for the Final Step of API Synthesis — Muneo Shoji, Yuko Suzumura, et al. · Organic Process Research & Development (2025) | TGRS Research Map | TGRS