Lithium Hydroxide → HCID 10127665, compound
Reaction equation
C([O:3][C:4](=[O:34])[CH2:5][N:6]1[C:14]2[C:9](=[CH:10][C:11]([O:15][CH2:16][C:17]3[S:21][C:20]([C:22]4[CH:27]=[CH:26][C:25]([C:28]([F:31])([F:30])[F:29])=[CH:24][CH:23]=4)=[N:19][C:18]=3[CH3:32])=[CH:12][CH:13]=2)[CH:8]=[C:7]1[CH3:33])C.[Li+].[OH-]>>[CH3:33][C:7]1[N:6]([CH2:5][C:4]([OH:34])=[O:3])[C:14]2[C:9]([CH:8]=1)=[CH:10][C:11]([O:15][CH2:16][C:17]1[S:21][C:20]([C:22]3[CH:23]=[CH:24][C:25]([C:28]([F:31])([F:29])[F:30])=[CH:26][CH:27]=3)=[N:19][C:18]=1[CH3:32])=[CH:12][CH:13]=2Participants
3
Procedure
In analogy to the procedure described in example 2 c], {2-methyl-5-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-indol-1-yl}-acetic acid ethyl ester was treated with LiOH to obtain {2-methyl-5-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-indol-1-yl}-acetic acid as off-white powder.
Sources & evidence
- ORD record
- ord-8bf277f5e3a94fed8d7467065eea4f05
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07235572B2
Reaction notes
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