Water → HCID 58021967, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]2[C:13]=1[C:12](=[O:14])[N:11]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([S:21][CH:22]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH3:23])[CH:16]=1)[C:10](=[O:30])[NH:9]2)=[O:4].O.C(=O)([O-])[OH:33].[Na+].OOS([O-])=O.[K+]>CC(C)=O>[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]2[C:13]=1[C:12](=[O:14])[N:11]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([S:21]([CH:22]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH3:23])=[O:33])[CH:16]=1)[C:10](=[O:30])[NH:9]2)=[O:4]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 5-methoxycarbonyl-3-[3-(1-phenyl -ethylthio)phenyl]thieno[3,4-d]pyrimidine-2,4(1H,3H)-dione (50 mg) in acetone (3 mL)-water (0.6 mL) were added sodium hydrogen carbonate (24 mg) and OXONE (registered trademark) (84 mg), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was extracted with ethyl acetate, and the extract was washed with 1 mol/L hydrochloric acid, water and brine successively, and dried over anhydrous magnesium sulfate.
Workup
- extractionThe reaction mixture was extracted with ethyl acetate
- washthe extract was washed with 1 mol/L hydrochloric acid, water and brine successively
- dry with materialdried over anhydrous magnesium sulfate
Sources & evidence
- ORD record
- ord-0232f9d7b1294c41be0d59d85b5a0bf3
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040693B2
Reaction notes
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