Hydrogen Peroxide → HCID 18697495, compound
Reaction equation
[CH3:1][C:2]1([CH3:11])[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[Se:4][NH:3]1.[OH:12]O>CO>[CH3:1][C:2]1([CH3:11])[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[Se:4](=[O:12])[NH:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The derivative 3,3-dimethyl-benzisoselenazoline BXT-51056 (212 mg; 1 mmole) was dissolved at room temperature in methanol (5 ml) with stirring. After addition of 5% hydrogen peroxide (600 μl; 1.05 mmole), stirring was continued for 15 min. The solvent was evaporated off under reduced pressure. The residue was taken up in 25 ml of dichloromethane and washed with 3×3 ml of a saturated NaCl solution, dried over Na2SO4 then filtered. After evaporation of the solvent under reduced pressure, the desired product was obtained in the form of yellowish crystals.
Workup
- stirringstirring
- customThe solvent was evaporated off under reduced pressure
- washwashed with 3×3 ml of a saturated NaCl solution
- dry with materialdried over Na2SO4
- filtrationthen filtered
- customAfter evaporation of the solvent under reduced pressure
Sources & evidence
- ORD record
- ord-aa15ec8b5cc449d39358cff0768b10f7
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06093532
Reaction notes
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