Lithium Hydroxide → HCID 11272830, compound
Reaction equation
C([O:3][C:4](=[O:41])[CH2:5][N:6]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([O:15][CH2:16][C:17]3[C:18]([CH:38]4[CH2:40][CH2:39]4)=[N:19][C:20]([C:27]4[CH:32]=[CH:31][C:30]([O:33][C:34]([F:37])([F:36])[F:35])=[CH:29][CH:28]=4)=[CH:21][C:22]=3[C:23]([F:26])([F:25])[F:24])[CH:13]=2)[CH:8]=[CH:7]1)C.[Li+].[OH-]>>[CH:38]1([C:18]2[C:17]([CH2:16][O:15][C:12]3[CH:13]=[C:14]4[C:9]([CH:8]=[CH:7][N:6]4[CH2:5][C:4]([OH:41])=[O:3])=[CH:10][CH:11]=3)=[C:22]([C:23]([F:24])([F:25])[F:26])[CH:21]=[C:20]([C:27]3[CH:28]=[CH:29][C:30]([O:33][C:34]([F:37])([F:36])[F:35])=[CH:31][CH:32]=3)[N:19]=2)[CH2:40][CH2:39]1Participants
3
Procedure
In analogy to the procedure described in example 5 g], {6-[2-cyclopropyl-6-(4-trifluoromethoxy-phenyl)-4-trifluoromethyl-pyridin-3-ylmethoxy]-indol-1-yl}-acetic acid ethyl ester was treated with LiOH to obtain the title compound as pink solid.
Sources & evidence
- ORD record
- ord-d92721939e2b415eaf9e93217e7f7bc8
- Source dataset
- uspto-grants-2006_02
- Patent number
- US06995263B2
Reaction notes
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