Organic Process Research and Development, volume 1, issue 3, pages 198-210

Development of a Manufacturing Process for Zatosetron Maleate

John E Burks
Leandro Espinosa
Elizabeth S LaBell
John M Mcgill
Allen R Ritter
Jeffery L Speakman
MARYANNE WILLIAMS
David A. Bradley
Moira G Haehl
Christopher R Schmid
Show full list: 10 authors
Publication typeJournal Article
Publication date1997-05-01
scimago Q1
SJR0.900
CiteScore6.9
Impact factor3.1
ISSN10836160, 1520586X
Organic Chemistry
Physical and Theoretical Chemistry
Abstract
Zatosetron maleate is a potent, selective 5-hydroxytryptamine receptor antagonist. In anticipation of commercialization, a manufacturing synthesis of zatosetron from tropinone and 5-chlorosalicylic acid was developed. Development efforts focused on addressing several key issues including the supply and quality of the critical raw material tropinone, improvements in the stereoselective formation of 3-endo-tropanamine, and the compatibility with existing manufacturing capabilities of process requirements for the Claisen rearrangement used to produce a crucial benzofuran intermediate. The results of these studies and an improved route to zatosetron maleate are described.
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