Reaction equation
[CH3:1][N:2]([CH3:27])[C:3]1[N:4]=[N:5][C:6]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[CH:18]=2)=[C:7]([C:9]2[CH:14]=[CH:13][N:12]=[C:11]([S:15][CH3:16])[N:10]=2)[CH:8]=1.OO.CO.C(OCC)(=[O:34])C.[OH2:38]>[O-][W]([O-])(=O)=O.[Na+].[Na+]>[CH3:27][N:2]([CH3:1])[C:3]1[N:4]=[N:5][C:6]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([C:23]([F:26])([F:25])[F:24])[CH:18]=2)=[C:7]([C:9]2[CH:14]=[CH:13][N:12]=[C:11]([S:15]([CH3:16])(=[O:34])=[O:38])[N:10]=2)[CH:8]=1Participants
7
Reactant 5
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 71 (112 mg, 0.286 mmol), sodium tungstate (10 mg, 0.02 mmol), 30% hydrogen peroxide (130 μL, 1.14 mmol), methanol (2.0 mL), and ethyl acetate (20 mL) were combined under Argon and heated to reflux for 3d. The solution was cooled, poured into water and extracted several times with ethyl acetate. The combined organic extracts were dried with anhydrous sodium sulfate. Removal of the solvent in vacuo gave 72 as a solid: 109 mg (0.259 mmol, 91%)
Workup
- temperatureheated
- temperatureThe solution was cooled
- extractionextracted several times with ethyl acetate
- dry with materialThe combined organic extracts were dried with anhydrous sodium sulfate
- customRemoval of the solvent in vacuo
Sources & evidence
- ORD record
- ord-bd9f0d4d6bbb4dd4b3bc580128c3cb66
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06602872B1
Linked notes
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