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.

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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

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article

Development and Scale-Up of an Enabling Synthetic Route to KTX-005, a Muscarinic Acetylcholine Receptor Agonist for the Potential Treatment of Schizophrenia

Vijaya Bhasker Gondi, Michel Leeman, Christopher R. H. Hale, Huaijun Zheng et al.
Organic Process Research & Development
Receptor Mechanisms and Signaling
article

Development and Scale-Up of an Enabling Synthetic Route to KTX-005, a Muscarinic Acetylcholine Receptor Agonist for the Potential Treatment of Schizophrenia

Vijaya Bhasker Gondi, Michel Leeman, Christopher R. H. Hale, Huaijun Zheng, Giorgio Attardo, Rui Zhang
article en

Abstract

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.

Organic Process Research & DevelopmentVol. 29(2)
WuXi AppTec (China) (CN), Bristol-Myers Squibb (United States) (US), Flevoziekenhuis (NL), Université Bourgogne Franche-Comté (FR)
Bristol-Myers Squibb
Good health and well-being
Openalex Percentile: Top 98%
Receptor Mechanisms and Signaling
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