Hydrogen Peroxide → HCID 14372165, compound
Reaction equation
[S:1]([C:5]1[O:13][C:12]2[C:7](=[N:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=1)(=[O:4])(=[O:3])[NH2:2].[OH:14]O.O>C(O)(=O)C>[S:1]([C:5]1[O:13][C:12]2[C:7](=[N+:8]([O-:14])[CH:9]=[CH:10][CH:11]=2)[CH:6]=1)(=[O:3])(=[O:4])[NH2:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a suspension of 2-sulfamoylfuro[3,2-b]pyridine (647 mg, 3.27 mmol) in glacial acetic acid (8 mL) was added 30% hydrogen peroxide (0.6 mL). This suspension was warmed at 60° C. for four hours to give a clear solution. Upon cooling the reaction mixture and adding water the product crystallized out. This pure product (444 mg, 63.5% yield) was collected by filtration, washed with water, ethanol and diethyl ether, mp: 236°-237° C. (decomposition).
Workup
- customto give a clear solution
- temperatureUpon cooling the reaction mixture
- customcrystallized out
Sources & evidence
- ORD record
- ord-b71766f77c814328a55713543aafb0f8
- Source dataset
- uspto-grants-1989_02
- Patent number
- US04808595
Reaction notes
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