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
Publication type: Journal Article
Publication date: 1997-05-01
scimago Q1
SJR: 0.900
CiteScore: 6.9
Impact factor: 3.1
ISSN: 10836160, 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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