Lansoprazole → HCID 10128985, compound
Reaction equation
[CH3:1][C:2]1[C:3]([CH2:14][S:15]([C:17]2[NH:21][C:20]3[CH:22]=[CH:23][CH:24]=[CH:25][C:19]=3[N:18]=2)=[O:16])=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]([F:13])([F:12])[F:11].C(N(CC)CC)C.Cl[S:34]([C:37]1[CH:42]=[CH:41][C:40]([NH:43][C:44]([NH2:46])=[O:45])=[CH:39][CH:38]=1)(=[O:36])=[O:35]>ClCCl>[CH3:1][C:2]1[C:3]([CH2:14][S:15]([C:17]2[N:18]([S:34]([C:37]3[CH:38]=[CH:39][C:40]([NH:43][C:44]([NH2:46])=[O:45])=[CH:41][CH:42]=3)(=[O:36])=[O:35])[C:19]3[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=3[N:21]=2)=[O:16])=[N:4][CH:5]=[CH:6][C:7]=1[O:8][CH2:9][C:10]([F:13])([F:11])[F:12]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-[[[3-Methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimidazole (185 mg) dissolved in 30 ml of dichloromethane and 0.4 ml of triethylamine was added to 128 mg of N-[4-(chlorosulfonyl)phenyl]urea. The reaction mixture was stirred at room temperature overnight. The reaction mixture was washed with water and 0.1N sodium bicarbonate solution.
Workup
- washThe reaction mixture was washed with water and 0.1N sodium bicarbonate solution
Sources & evidence
- ORD record
- ord-96d30534e1294c18bfb274f277025208
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06559167B1
Reaction notes
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