Benzaldehyde → HCID 9795164, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8]([NH2:11])(=[O:10])=[O:9].[CH:12](=O)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[C:13]1([CH:12]2[NH:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=3[S:8](=[O:9])(=[O:10])[NH:11]2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Participants
3
Procedure
2-Aminobenzenesulfonamide was transformed by Method G (using benzaldehyde). M.p. 125.5-128.5° C.
Sources & evidence
- ORD record
- ord-388d8104b382456db818a0b63fcdbd8f
- Source dataset
- uspto-grants-2005_09
- Patent number
- US06943159B1
Reaction notes
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