Sodium Hydroxide → (4-{3-[4-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-indol-1-yl)-acetic acid
Reaction equation
C([O:5][C:6](=[O:37])[CH2:7][N:8]1[C:16]2[C:11](=[C:12]([O:17][CH2:18][CH2:19][CH2:20][C:21]3[S:25][C:24]([C:26]4[CH:31]=[CH:30][C:29]([C:32]([F:35])([F:34])[F:33])=[CH:28][CH:27]=4)=[N:23][C:22]=3[CH3:36])[CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9]1)(C)(C)C.[OH-].[Na+]>>[CH3:36][C:22]1[N:23]=[C:24]([C:26]2[CH:27]=[CH:28][C:29]([C:32]([F:35])([F:34])[F:33])=[CH:30][CH:31]=2)[S:25][C:21]=1[CH2:20][CH2:19][CH2:18][O:17][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:11]=1[CH:10]=[CH:9][N:8]2[CH2:7][C:6]([OH:37])=[O:5]Participants
3
Procedure
In analogy to the procedure described in example 2 c], (4-{3-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-indol-1-yl)-acetic acid tert-butyl ester was treated with NaOH to obtain (4-{3-[4-methyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-yl]-propoxy}-indol-1-yl)-acetic acid as white solid.
Sources & evidence
- ORD record
- ord-b7a1f0986ea1440aa0c71f21e2f03145
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07235572B2
Reaction notes
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