Lithium Hydroxide → 3-(4-{Cyclopentyl-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-methoxy}-2-methyl-phenyl)-2-ethoxy-propionic acid
Reaction equation
C([O:3][C:4](=[O:40])[CH:5]([O:37][CH2:38][CH3:39])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH:14]([CH:31]2[CH2:35][CH2:34][CH2:33][CH2:32]2)[C:15]2[S:19][C:18]([C:20]3[CH:25]=[CH:24][C:23]([C:26]([F:29])([F:28])[F:27])=[CH:22][CH:21]=3)=[N:17][C:16]=2[CH3:30])=[CH:9][C:8]=1[CH3:36])C.[Li+].[OH-]>>[CH:31]1([CH:14]([C:15]2[S:19][C:18]([C:20]3[CH:25]=[CH:24][C:23]([C:26]([F:28])([F:29])[F:27])=[CH:22][CH:21]=3)=[N:17][C:16]=2[CH3:30])[O:13][C:10]2[CH:11]=[CH:12][C:7]([CH2:6][CH:5]([O:37][CH2:38][CH3:39])[C:4]([OH:40])=[O:3])=[C:8]([CH3:36])[CH:9]=2)[CH2:35][CH2:34][CH2:33][CH2:32]1Participants
3
Reactant 2
Product 1
Procedure
In analogy to the procedure described in example 10 d], 3-(4-{cyclopentyl-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-methoxy}-2-methyl-phenyl)-2-ethoxy-propionic acid ethyl ester (mixture of two diastereomeric racemates) was treated with LiOH to obtain 3-(4-{cyclopentyl-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-methoxy}-2-methyl-phenyl)-2-ethoxy-propionic acid as a mixture of two diastereomeric racemates as colorless liquid.
Workup
- customdescribed in example 10 d
Sources & evidence
- ORD record
- ord-b345ba45a43a40469c4da6ac85d33104
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06809110B2
Reaction notes
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