Lithium Hydroxide → HCID 60142089, compound

HRID 572476Notes

Reaction equation

HRID 572476 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

4

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

  1. customwas consumed
  2. temperaturecooled to RT
  3. customremoved the solvent
  4. additionadded water
  5. extractionextracted with EA
  6. customto remove impurity
  7. extractionextracted with EA
  8. washthe organic layer was washed with water and brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated to dryness

Sources & evidence

ORD record
ord-b7dda5c21057436d8e3d17cfc23e25b3
Source dataset
uspto-grants-2015_05
Patent number
US09029391B2

Reaction notes

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