Hydrogen Peroxide → HCID 178418510, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([S:9]([CH3:11])=[O:10])[CH:6]=[CH:5][C:4]=1[C:12]1[N:13]=[C:14]2[C:19](=[O:20])[NH:18][NH:17][CH:16]=[C:15]2[N:21]=1.[OH:22]O>C(O)(=O)C>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([S:9]([CH3:11])(=[O:22])=[O:10])[CH:6]=[CH:5][C:4]=1[C:12]1[N:13]=[C:14]2[C:19](=[O:20])[NH:18][NH:17][CH:16]=[C:15]2[N:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A quantity of 0.07 gm of 2-(2-methoxy-4-methylsulfinyl-phenyl)-5H-imidazo[4,5-d]pyridazin-4-one is dissolved in 5 ml of glacial acetic acid, mixed with 0.05 ml of 30% hydrogen peroxide, and stirred first for 55 minutes at ambient temperature then for two hours at 40°-50° C., Then, a further 0.05 ml of hydrogen peroxide are added, and the mixture is heated for another hour. The product precipitated is subjected to suction filtration and washed with ether.
Workup
- waitfor two hours at 40°-50° C.
- temperaturethe mixture is heated for another hour
- customThe product precipitated
- filtrationis subjected to suction filtration
- washwashed with ether
Sources & evidence
- ORD record
- ord-033061a22a0d4381887b3730bf5da3c7
- Source dataset
- uspto-grants-1988_02
- Patent number
- US04722929
Reaction notes
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