Lithium hydroxide, monohydrate → HCID 68931117, compound
Reaction equation
[CH3:1][C@@H:2]1[CH2:7][N:6]([C@@H:8]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:9]2[CH:14]=[CH:13][C:12]([C:15]#[C:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11][CH:10]=2)[CH2:5][CH2:4][N:3]1[CH2:29][C:30]([O:32]C(C)(C)C)=[O:31].O.[OH-].[Li+]>C1COCC1.CO.O>[CH3:1][C@@H:2]1[CH2:7][N:6]([C@@H:8]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:9]2[CH:10]=[CH:11][C:12]([C:15]#[C:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:13][CH:14]=2)[CH2:5][CH2:4][N:3]1[CH2:29][C:30]([OH:32])=[O:31]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl 2-((R)-2-methyl-4-((S)-phenyl(4-(2-phenylethynyl)phenyl)-methyl)piperazin-1-yl)acetate (320 mg, 0.666 mmol) in THF/MeOH/H2O=5:5:1 (5.5 mL) was added lithium hydroxide monohydrate (279 mg, 6.658 mmol) and the resulting solution was stirred overnight. The solvent was evaporated to dryness under high vacuum and the residue was diluted with water, adjusted pH=5, extracted with DCM, dried over Na2SO4, filtered and evaporated to dryness. The residue was loaded onto flash column (SiO2, DCM to DCM/MeOH=100:5 to 100:10 to 100:15 to 100:20) to give 2-((R)-2-methyl-4-((S)-phenyl(4-(2-phenylethynyl)phenyl)methyl)piperazin-1-yl)acetic acid (240 mg) as a white solid.
Workup
- customThe solvent was evaporated to dryness under high vacuum
- additionthe residue was diluted with water, adjusted pH=5
- extractionextracted with DCM
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-bdf135a052e64ca3a1e504c930fc4dc3
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07538114B2
Reaction notes
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