Water → Rabeprazole

HRID 556011Notes

Reaction equation

HRID 556011 reaction equation
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][S:14][C:15]2[NH:19][C:18]3[CH:20]=[CH:21][CH:22]=[CH:23][C:17]=3[N:16]=2)[C:8]=1[CH3:24].[OH-:25].[Na+].O>ClCCl>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([CH2:13][S:14]([C:15]2[NH:16][C:17]3[CH:23]=[CH:22][CH:21]=[CH:20][C:18]=3[N:19]=2)=[O:25])[C:8]=1[CH3:24]

Participants

5

Procedure

2-[{4-(3-Methoxypropoxy)-3-methylpyridin-2-yl}methylthio]-1H-benzimidazole (25.0 g (72.8 mmol)) was dissolved in dichloromethane and cooled. Then, mcpba (70.2% purity; 8.95 g (36.4 mmol)) was added gradually so that the internal temperature did not exceed −15° C. 10% Aqueous sodium hydroxide solution (70.8 ml) was then added, and after stirring and still standing the water layer was separated. The separated water layer was washed with dichloromethane (48 ml) twice. After addition of a 2N-ammonium acetate aqueous solution, the water layer was extracted with dichloromethane (48 ml) twice. The dichloromethane layer was washed with water (48 ml) twice, concentrated under a reduced pressure, crystallized with toluene (110 ml), and filtered to obtain 2-[{4-(3-methoxypropoxy)-3-methylpyridin-2-yl}methylsulfinyl]-1H-benzimidazole (10.6 g) (HPLC purity 99.6%, yield 40.4%).

Workup

  1. temperaturecooled
  2. additionThen, mcpba (70.2% purity; 8.95 g (36.4 mmol)) was added gradually so that the internal temperature
  3. customdid not exceed −15° C
  4. customwas separated
  5. washThe separated water layer was washed with dichloromethane (48 ml) twice
  6. additionAfter addition of a 2N-ammonium acetate aqueous solution
  7. extractionthe water layer was extracted with dichloromethane (48 ml) twice
  8. washThe dichloromethane layer was washed with water (48 ml) twice
  9. concentrationconcentrated under a reduced pressure
  10. customcrystallized with toluene (110 ml)
  11. filtrationfiltered

Sources & evidence

ORD record
ord-897f65de6c564b35993b21570db5ee73
Source dataset
uspto-grants-2011_11
Patent number
US08053580B2

Reaction notes

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