Sodium Hydroxide → [Rac]-2-{2-methyl-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-benzyl}-heptanoic acid
Reaction equation
C[O:2][C:3](=[O:36])[CH:4]([CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH2:18][C:19]2[S:23][C:22]([C:24]3[CH:29]=[CH:28][C:27]([C:30]([F:33])([F:32])[F:31])=[CH:26][CH:25]=3)=[N:21][C:20]=2[CH3:34])=[CH:13][C:12]=1[CH3:35])[CH2:5][CH2:6][CH2:7][CH2:8][CH3:9].[OH-].[Na+]>>[CH3:35][C:12]1[CH:13]=[C:14]([O:17][CH2:18][C:19]2[S:23][C:22]([C:24]3[CH:25]=[CH:26][C:27]([C:30]([F:33])([F:32])[F:31])=[CH:28][CH:29]=3)=[N:21][C:20]=2[CH3:34])[CH:15]=[CH:16][C:11]=1[CH2:10][CH:4]([CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[C:3]([OH:36])=[O:2]Participants
3
Procedure
In analogy to the procedure described in example 10 d], [rac]-2-{2-methyl-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-benzyl}-heptanoic acid methyl ester was treated with 3 N NaOH to obtain [rac]-2-{2-methyl-4-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-benzyl}-heptanoic acid as yellow crystals.
Workup
- customdescribed in example 10 d
Sources & evidence
- ORD record
- ord-fc4198e3faef417e867b579447fc4e24
- Source dataset
- uspto-grants-2004_10
- Patent number
- US06809110B2
Reaction notes
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