N-(4-Aminophenyl)-N-methylmethanesulfonamide → HCID 178468603, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=2)[C:6](=[C:18](OCC)[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:5]1=[O:28])(=O)C.[NH2:29][C:30]1[CH:35]=[CH:34][C:33]([N:36]([CH3:41])[S:37]([CH3:40])(=[O:39])=[O:38])=[CH:32][CH:31]=1>>[CH3:41][N:36]([S:37]([CH3:40])(=[O:39])=[O:38])[C:33]1[CH:32]=[CH:31][C:30]([NH:29]/[C:18](=[C:6]2\[C:5](=[O:28])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:11]=3)/[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[CH:35][CH:34]=1Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenylmethylene)-6-ethoxycarbonyl-2-indolinone and N-(4-aminophenyl)-N-methyl-methanesulphonamide Rf value: 0.8 (aluminium oxide, ethyl acetate) C26H25N3O5S
Sources & evidence
- ORD record
- ord-ddfe7badf2554c9bae49d0e743f8f940
- Source dataset
- uspto-grants-2004_07
- Patent number
- US06762180B1
Reaction notes
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