4-(Methylsulfonamido)aniline → HCID 178456779, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=2)[C:6](=[C:17](OCC)[CH2:18][CH3:19])[C:5]1=[O:23])(=O)C.[CH3:24][S:25]([NH:28][C:29]1[CH:34]=[CH:33][C:32]([NH2:35])=[CH:31][CH:30]=1)(=[O:27])=[O:26]>>[CH3:24][S:25]([NH:28][C:29]1[CH:34]=[CH:33][C:32]([NH:35]/[C:17](=[C:6]2\[C:5](=[O:23])[NH:4][C:12]3[C:7]\2=[CH:8][C:9]([O:15][CH3:16])=[C:10]([O:13][CH3:14])[CH:11]=3)/[CH2:18][CH3:19])=[CH:31][CH:30]=1)(=[O:27])=[O:26]Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-ethyl-methylidene)-5,6-dimethoxy-2-indolinone and N-methylsulphonyl-p-phenylenediamine
Sources & evidence
- ORD record
- ord-4bdf53f8dec840bf9e655b9e6e89ace9
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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