Water → Ammonium Hydroxide

HRID 1442874Notes

Reaction equation

HRID 1442874 reaction equation
[C:1]1([C:7]2[CH:11]=[N:10][C:9](=[O:12])[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Na+].Br[CH2:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18].O>CN(C=O)C>[NH4+:8].[OH-:12].[O:12]=[C:9]1[NH:8][C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[CH:11][N:10]1[CH2:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18]

Participants

7

Conditions

Temperature
0 °C

Procedure

To a stirred solution of 4-phenylimidazol-2-one from Step A (1.00 g, 6.24 mmol) in DMF (10 mL) at 0° C. was added sodium hydride (300 mg of a 60% dispersion in mineral oil, 7.49 mmol). The mixture was stirred at 0° C. for 1 h, then tert-butyl bromoacetate (1.47 g, 7.49 mmol) was added. The reaction mixture was allowed to warm to ambient temperature and stirring was continued for 18 h. The reaction mixture was poured into water and extracted with CH2Cl2 (3×). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo to give a crude product, which was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH:NH4OH—100:0:0 to 90:5:0.5 to provide the title compound. MS: m/z=275 (M+1).

Workup

  1. temperatureto warm to ambient temperature
  2. stirringstirring
  3. waitwas continued for 18 h
  4. extractionextracted with CH2Cl2 (3×)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customto give a crude product, which
  9. customwas purified by silica gel chromatography
  10. washeluting with a gradient of CH2Cl2

Sources & evidence

ORD record
ord-8b85ed616fe44227a71a2c7a1825117f
Source dataset
uspto-grants-2010_02
Patent number
US07659300B2

Reaction notes

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