4-(2-Dimethylamino-ethylsulphonylamino)-aniline → HCID 178483990, compound
Reaction equation
C(O[C:4](=[C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[NH:13][C:12]1=[O:20])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)C.[CH3:21][N:22]([CH3:36])[CH2:23][CH2:24][S:25]([NH:28][C:29]1[CH:35]=[CH:34][C:32]([NH2:33])=[CH:31][CH:30]=1)(=[O:27])=[O:26]>>[CH3:21][N:22]([CH3:36])[CH2:23][CH2:24][S:25]([NH:28][C:29]1[CH:35]=[CH:34][C:32]([NH:33]/[C:4](=[C:11]2\[C:12](=[O:20])[NH:13][C:14]3[C:19]\2=[CH:18][CH:17]=[CH:16][CH:15]=3)/[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][CH:10]=2)=[CH:31][CH:30]=1)(=[O:27])=[O:26]Participants
3
Procedure
Prepared analogously to Example 39 from 3-(1-ethoxy-1-phenyl-methylidene)-2-indolinone and 4-(2-dimethylamino-ethylsulphonylamino)-aniline.
Sources & evidence
- ORD record
- ord-3ea450a54cad486d961aa20d218f03f0
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855710B2
Reaction notes
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