Hydrochloric Acid → HCID 59275775, compound

HRID 1688306Notes

Reaction equation

HRID 1688306 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:16]=[C:17]([C:20]2[CH:21]=[CH:22][C:23]3[O:27][C:26]([C:28]4[CH:33]=[CH:32][C:31]([F:34])=[CH:30][CH:29]=4)=[C:25]([C:35](=[O:38])[NH:36][CH3:37])[C:24]=3[CH:39]=2)[C:18]=1[CH3:19])[C:12]([O:14]C)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].Cl>CO.C1COCC1>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:16]=[C:17]([C:20]2[CH:21]=[CH:22][C:23]3[O:27][C:26]([C:28]4[CH:29]=[CH:30][C:31]([F:34])=[CH:32][CH:33]=4)=[C:25]([C:35](=[O:38])[NH:36][CH3:37])[C:24]=3[CH:39]=2)[C:18]=1[CH3:19])[C:12]([OH:14])=[O:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Conditions

Temperature
60 °C

Procedure

To a mixture of methyl 3-(benzyloxy)-5-(2-(4-fluorophenyl)-3-(methylcarbamoyl)benzofuran-5-yl)-4-methylbenzoate (0.3 g, 0.57 mmol, 1 eq) in a 1:1 mixture of MeOH/THF at ambient temperature was added 5 eq. of NaOH, and the resulting mixture was heated to 60° C. for 5 h. The mixture was cooled to ambient temperature and then cooled in ice-water bath. The reaction mixture was acidified with 1.5 N HCl and then concentrated. The mixture with white precipitates was diluted with water and filtered to get the solid. It is further washed with water and dried in vacuum. Yield: 0.2 g (70%). 1H NMR (400 MHz, DMSO-d6): δ 2.19 (s, 3H), 2.82-2.83 (d, 3H, J=4.56 Hz), 5.27 (s, 2H), 7.34-7.46 (m, 6H), 7.50-7.55 (m, 4H), 7.60 (s, 1H), 7.75-7.77 (d, 1H, J=8.44 Hz), 7.99-8.03 (m, 2H), 8.49-8.50 (d, 1H), 13.0 (s, 1H). LCMS: (ES+) m/z=510 (M+H). Ascentis Express C18 (5.0×2.1-2.7 μm) Mphase A: 2% MeCN-98% H2O-10 mM NH4COOH Mphase B: 98% MeCN-2% H2O-10 mM NH4COOH

Workup

  1. temperatureThe mixture was cooled to ambient temperature
  2. concentrationconcentrated
  3. customThe mixture with white precipitates
  4. additionwas diluted with water
  5. filtrationfiltered
  6. customto get the solid
  7. washIt is further washed with water
  8. customdried in vacuum

Sources & evidence

ORD record
ord-4a83fa4bbb2d45119098ac1de1d05ebd
Source dataset
uspto-grants-2012_04
Patent number
US08148382B2

Reaction notes

Loading…