Development of the Commercial Manufacturing Process for Xanomeline Tartrate, an Active Pharmaceutical Ingredient in KarXT

Development of the commercial manufacturing strategy and process employed for xanomeline tartrate ( KTX-001), a key active pharmaceutical ingredient (API) in KarXT, is described. The development process involved identifying efficient processes for key bond-forming steps, including the conversion of regulatory starting material nicotinaldehyde ( 1 ) to stage 1 regulatory intermediate chlorothiadiazole 2, nucleophilic aromatic displacement of the chlorine atom within 2 with 1-hexanol followed by methylation to generate stage 2 regulatory intermediate pyridinium 4, and selective partial reduction of the pyridine ring to produce the API freebase, which after tartrate salt formation gave access to stage 3 regulatory intermediate crude xanomeline tartrate ( crude KTX-001 ). A recrystallization process was developed to provide the drug substance xanomeline tartrate ( KTX-001 ) in an overall yield of 35% from nicotinaldehyde ( 1 ) with HPLC purity of >99.0% on scales of 500+ kilograms per batch, suitable for reliable supply of this commercial drug substance.

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Publication Details

Journal
Organic Process Research & Development
Published
2026-07-16
DOI
https://doi.org/10.1021/acs.oprd.6c00185
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
0.00

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article

Development of the Commercial Manufacturing Process for Xanomeline Tartrate, an Active Pharmaceutical Ingredient in KarXT

Vijaya Bhasker Gondi, Rajender Vemula, Aida Ajaz, Christopher R. H. Hale et al.
Organic Process Research & Development
Drug Solubulity and Delivery Systems
article

Development of the Commercial Manufacturing Process for Xanomeline Tartrate, an Active Pharmaceutical Ingredient in KarXT

Vijaya Bhasker Gondi, Rajender Vemula, Aida Ajaz, Christopher R. H. Hale, Yolanda Gasanz, Giorgio Attardo, Joseph Ryan, MVRCH Murthy
article en

Abstract

Development of the commercial manufacturing strategy and process employed for xanomeline tartrate ( KTX-001), a key active pharmaceutical ingredient (API) in KarXT, is described. The development process involved identifying efficient processes for key bond-forming steps, including the conversion of regulatory starting material nicotinaldehyde ( 1 ) to stage 1 regulatory intermediate chlorothiadiazole 2, nucleophilic aromatic displacement of the chlorine atom within 2 with 1-hexanol followed by methylation to generate stage 2 regulatory intermediate pyridinium 4, and selective partial reduction of the pyridine ring to produce the API freebase, which after tartrate salt formation gave access to stage 3 regulatory intermediate crude xanomeline tartrate ( crude KTX-001 ). A recrystallization process was developed to provide the drug substance xanomeline tartrate ( KTX-001 ) in an overall yield of 35% from nicotinaldehyde ( 1 ) with HPLC purity of >99.0% on scales of 500+ kilograms per batch, suitable for reliable supply of this commercial drug substance.

Organic Process Research & Development
Bristol-Myers Squibb (Netherlands) (NL), Dr. Reddy's Laboratories (India) (IN), Bristol-Myers Squibb (United Kingdom) (GB), Esteve Química (Spain) (ES), Esteve (Spain) (ES)
Bristol-Myers Squibb Foundation
Industry, innovation and infrastructure
Openalex Percentile: Top 10%
Drug Solubulity and Delivery Systems
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