Chemo-Enzymatic Synthesis of Enantiopure β-Antagonist (S)-Betaxolol

The β-blocker (S)-betaxolol has been synthesized in 99% enantiomeric excess (ee) from the commercially available precursor 4-(2-hydroxyethyl)phenol. The racemic chlorohydrin 1-chloro-3-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)propan-2-ol was esterified with vinyl acetate catalyzed by lipase B from Ca...

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Bibliographic Details
Published in:Catalysts
Main Authors: Susanne Hansen Troøyen, Elisabeth Egholm Jacobsen
Format: Text
Language:English
Published: Multidisciplinary Digital Publishing Institute 2022
Subjects:
( S )-betaxolol
enantiopure building blocks
Candida antarctica lipase B
chiral chromatography
Antarc*
Antarctica
Online Access:https://doi.org/10.3390/catal12121645
Description
Summary:The β-blocker (S)-betaxolol has been synthesized in 99% enantiomeric excess (ee) from the commercially available precursor 4-(2-hydroxyethyl)phenol. The racemic chlorohydrin 1-chloro-3-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)propan-2-ol was esterified with vinyl acetate catalyzed by lipase B from Candida antarctica, which gave the R-chlorhydrin (R)-1-chloro-3-(4-(2-(cyclopropylmethoxy)ethyl)phenoxy)propan-2-ol in 99% ee with 38% yield. The enantiomeric excess of the R-chlorohydrin was retained in an amination reaction with isopropylamine in methanol to yield (S)-betaxolol in 99% ee and with 9% overall yield. We are under way to improve the yield.

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