Lithium hydroxide, monohydrate → HCID 86731634, compound
Reaction equation
[F:1][C:2]([F:33])([F:32])[O:3][C:4]1[CH:5]=[C:6]([CH:29]=[CH:30][CH:31]=1)[CH2:7][N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@@H:9]1[C:14]([NH:16][C@H:17]([C:19]1[CH:28]=[CH:27][C:22]([C:23]([O:25]C)=[O:24])=[CH:21][CH:20]=1)[CH3:18])=[O:15].O[Li:35].O>>[F:32][C:2]([F:1])([F:33])[O:3][C:4]1[CH:5]=[C:6]([CH:29]=[CH:30][CH:31]=1)[CH2:7][N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][C@@H:9]1[C:14]([NH:16][C@H:17]([C:19]1[CH:28]=[CH:27][C:22]([C:23]([O-:25])=[O:24])=[CH:21][CH:20]=1)[CH3:18])=[O:15].[Li+:35]Participants
3
Procedure
The title compound (E8) (51 mg) was prepared according to the general procedure for esters hydrolysis starting from methyl 4-((S)-1-((R)-1-(3-(trifluoromethoxy)benzyl)piperidine-2-carboxamido)ethyl)benzoate (D25) (52 mg). (LiOH H2O: 3 eq; reaction time: 3 hrs)
Sources & evidence
- ORD record
- ord-058385bc9feb419aaf0ffcafe738fa64
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09120824B2
Reaction notes
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