Development and Scale-Up of an Enabling Synthetic Route to <b>KTX-005</b>, a Muscarinic Acetylcholine Receptor Agonist for the Potential Treatment of Schizophrenia
Development and optimization of phase-appropriate synthetic technologies to prepare KTX-005, a potent muscarinic acetylcholine receptor agonist, are described in this article. The modular strategy involves three building blocks: commercially available materials dichlorothiadiazole (21), butanethiol (22), and custom-synthesized azabicyclo derivative (18). The highlight of the enabling synthetic strategy toward KTX-005 is a unique thiadiazole ring opening/closing sequence to facilitate both dichlorothiadiazole desymmetrization with butanethiol as well as functionalization of the azabicyclo ring derivative 18.
Authors
- Vijaya Bhasker Gondi (ORCID: https://orcid.org/0000-0003-2096-3077)
- Michel Leeman (ORCID: https://orcid.org/0000-0002-8854-1084)
- Christopher R. H. Hale (ORCID: https://orcid.org/0009-0002-9925-5750)
- Huaijun Zheng (ORCID: https://orcid.org/0009-0007-0126-3717)
- Giorgio Attardo
- Rui Zhang (ORCID: https://orcid.org/0000-0002-1360-2452)
Institutions
- WuXi AppTec (China) (CN)
- Bristol-Myers Squibb (United States) (US)
- Flevoziekenhuis (NL)
- Université Bourgogne Franche-Comté (FR)
Publication Details
- Journal
- Organic Process Research & Development
- Published
- 2025-02-06
- DOI
- https://doi.org/10.1021/acs.oprd.4c00531
- Primary Topic
- Receptor Mechanisms and Signaling
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Bristol-Myers Squibb