Potassium Permanganate → HCID 10295553, compound
Reaction equation
[CH:1]1([S:6]([CH:8]([C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[C:19]([Cl:24])[CH:18]=2)[C:9]([NH:11][C:12]2[S:13][CH:14]=[CH:15][N:16]=2)=[O:10])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.[Mn]([O-])(=O)(=O)=[O:26].[K+]>CO.O>[CH:1]1([S:6]([CH:8]([C:17]2[CH:22]=[CH:21][C:20]([Cl:23])=[C:19]([Cl:24])[CH:18]=2)[C:9]([NH:11][C:12]2[S:13][CH:14]=[CH:15][N:16]=2)=[O:10])(=[O:26])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 25 °C
Procedure
A solution of rac-2-cyclopentanesulfinyl-2-(3,4-dichloro-phenyl)-N-thiazol-2-yl-acetamide (20 mg, 0.05 mmol) in methanol (2 mL) was stirred at 25° C. as a solution of potassium permanganate (9 mg, 0.06 mmol) in water (0.5 mL) was added. The mixture was stirred at 25° C. for 30 min and then was filtered. The filter cake was washed with dichloromethane and the combined filtrates were washed with sodium bicarbonate solution (10 mL) and brine (10 mL), then were dried over sodium sulfate, filtered and concentrated in vacuo. The product was purified by chromatography (Biotage Flash 12M column, 50/50 hexanes/ethyl acetate) to provide rac-2-cyclopentanesulfonyl-2-(3,4-dichloro-phenyl)-N-thiazol-2-yl-acetamide(10 mg, 48% yield) as a colorless oil: EI-HRMS m/e calculated for C16H16N2O3S2Cl2 (M+) 417.9979, found 417.9977.
Workup
- additionwas added
- filtrationwas filtered
- washThe filter cake was washed with dichloromethane
- washthe combined filtrates were washed with sodium bicarbonate solution (10 mL) and brine (10 mL)
- dry with materialwere dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe product was purified by chromatography (Biotage Flash 12M column, 50/50 hexanes/ethyl acetate)
Sources & evidence
- ORD record
- ord-302f7e96b365477a8a1ebedc66d5ee76
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06486184B2
Reaction notes
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