Lithium Hydroxide → HCID 22647441, compound
Reaction equation
C([O:3][C:4](=[O:38])[CH:5]([O:35][CH2:36][CH3:37])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH:14]([C:18]2[S:22][C:21]([C:23]3[CH:28]=[CH:27][C:26]([C:29]([F:32])([F:31])[F:30])=[CH:25][CH:24]=3)=[N:20][C:19]=2[CH3:33])[CH2:15][CH:16]=[CH2:17])=[CH:9][C:8]=1[CH3:34])C.[Li+].[OH-]>>[CH2:36]([O:35][CH:5]([CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH:14]([C:18]2[S:22][C:21]([C:23]3[CH:24]=[CH:25][C:26]([C:29]([F:30])([F:31])[F:32])=[CH:27][CH:28]=3)=[N:20][C:19]=2[CH3:33])[CH2:15][CH:16]=[CH2:17])=[CH:9][C:8]=1[CH3:34])[C:4]([OH:38])=[O:3])[CH3:37]Participants
3
Procedure
In analogy to the procedure described in example 10 d], 2-ethoxy-3-(2-methyl-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-but-3-enyloxy}-phenyl)-propionic acid ethyl ester (mixture of two diastereomeric racemates) was treated with LiOH to obtain 2-ethoxy-3-(2-methyl-4-{1-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-but-3-enyloxy}-phenyl)-propionic acid as a mixture of two diastereomeric racemates as colorless solid.
Workup
- customdescribed in example 10 d
Sources & evidence
- ORD record
- ord-6c7f629a77dd4f299d1e4d4099cc6fcb
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06809110B2
Reaction notes
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