Lithium Hydroxide → HCID 60142089, compound
Reaction equation
C[O:2][C:3](=[O:30])[CH:4]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])[C:5]1[N:6]([CH3:24])[C:7](=[O:23])[C:8]2[C:13]([C:14]=1[C:15]1[CH:20]=[CH:19][C:18]([F:21])=[C:17]([F:22])[CH:16]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2.[Li+].[OH-]>C1COCC1>[C:26]([O:25][CH:4]([C:5]1[N:6]([CH3:24])[C:7](=[O:23])[C:8]2[C:13]([C:14]=1[C:15]1[CH:20]=[CH:19][C:18]([F:21])=[C:17]([F:22])[CH:16]=1)=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:3]([OH:30])=[O:2])([CH3:29])([CH3:28])[CH3:27]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a solution of tert-Butoxy-[4-(3,4-Difluoro-phenyl)-2-methyl-1-oxo-1,2-dihydro-isoquinolin-3-yl]-acetic acid methyl ester (72 mg, 0.15 mmol) in THF (2.0 ml) was added an aqueous LiOH (1 N, 0.69 ml). The mixture was stirred at 60° C. overnight. LCMS showed SM was consumed, cooled to RT, removed the solvent, added water, extracted with EA to remove impurity, the aqueous layer was adjusted to pH=6 with 1N HCl, extracted with EA, the organic layer was washed with water and brine, dried over Na2SO4, filtered, concentrated to dryness, gave the desired product. (m=46 mg, Yield: 66%). 1HNMR: (400 MHz, d6-DMSO) δ 0.91 (s, 5H), 1.00 (s, 4H), 3.56 (s, 1.67H), 3.63 (s, 1.33H), 4.93 (s, 1H), 6.84 (d, J=8.0 Hz, 0.5H), 6.99 (d, J=8.0 Hz, 0.5H), 7.15 (s, 0.5H), 7.30 (m, 1H), 7.44 (m, 0.5H), 7.60 (m, 3H), 8.28 (d, J=8.0 Hz, 1H).
Workup
- customwas consumed
- temperaturecooled to RT
- customremoved the solvent
- additionadded water
- extractionextracted with EA
- customto remove impurity
- extractionextracted with EA
- washthe organic layer was washed with water and brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated to dryness
Sources & evidence
- ORD record
- ord-b7dda5c21057436d8e3d17cfc23e25b3
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09029391B2
Reaction notes
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