Hydrogen Peroxide → HCID 20210490, compound
Reaction equation
[OH:1]O.[CH2:3]([S:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[NH:13][C:14]3[C:19]([N:20]=2)=[CH:18][N:17]=[N:16][CH:15]=3)=[C:8]([O:21][CH3:22])[CH:7]=1)[CH3:4]>C(O)C>[CH2:3]([S:5]([C:6]1[CH:11]=[CH:10][C:9]([C:12]2[NH:20][C:19]3[C:14]([N:13]=2)=[CH:15][N:16]=[N:17][CH:18]=3)=[C:8]([O:21][CH3:22])[CH:7]=1)=[O:1])[CH3:4]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
10 ml of 30% strength H2O2 are added to a boiling solution of 2.84 g of 2-(4-ethylthio-2-methoxyphenyl)-1,3,5,6-tetraazaindene in 50 ml of ethanol, and the mixture is then boiled for 3 hours. Cooling down and customary working up gives 2-(4-ethylsulfinyl-2-methoxyphenyl)-1,3,5,6-tetraazaindene.
Workup
- temperatureCooling down and
Sources & evidence
- ORD record
- ord-46658899668144d9aa7e3cf4b2b3ee2b
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04477454
Reaction notes
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