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.
Authors
- Vijaya Bhasker Gondi (ORCID: https://orcid.org/0000-0003-2096-3077)
- Rajender Vemula (ORCID: https://orcid.org/0000-0002-7214-1094)
- Aida Ajaz
- Christopher R. H. Hale (ORCID: https://orcid.org/0009-0002-9925-5750)
- Yolanda Gasanz
- Giorgio Attardo
- Joseph Ryan
- MVRCH Murthy
Institutions
- Bristol-Myers Squibb (Netherlands) (NL)
- Dr. Reddy's Laboratories (India) (IN)
- Bristol-Myers Squibb (United Kingdom) (GB)
- Esteve Química (Spain) (ES)
- Esteve (Spain) (ES)
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
Funders
- Bristol-Myers Squibb Foundation