4-[N-(2-dimethylamino-ethyl)-N-methylsulphonyl-amino]-aniline → HCID 178483743, compound
Reaction equation
CO[C:3](=[C:10]1[C:18]2[C:13](=[CH:14][C:15]3[O:21][CH2:20][O:19][C:16]=3[CH:17]=2)[NH:12][C:11]1=[O:22])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:23][N:24]([CH3:39])[CH2:25][CH2:26][N:27]([S:35]([CH3:38])(=[O:37])=[O:36])[C:28]1[CH:33]=[CH:32][C:31]([NH2:34])=[CH:30][CH:29]=1>>[CH3:23][N:24]([CH3:39])[CH2:25][CH2:26][N:27]([C:28]1[CH:29]=[CH:30][C:31]([NH:34]/[C:3](=[C:10]2\[C:11](=[O:22])[NH:12][C:13]3[C:18]\2=[CH:17][C:16]2[O:19][CH2:20][O:21][C:15]=2[CH:14]=3)/[C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)=[CH:32][CH:33]=1)[S:35]([CH3:38])(=[O:37])=[O:36]Participants
3
Procedure
Prepared from 3-(1-methoxy-1-phenyl-methylidene)-5,6-methylenedioxy-2-indolinone and N-(2-dimethylamino-ethyl)-N-methylsulphonyl-p-phenylenediamine
Sources & evidence
- ORD record
- ord-5bed22c3367d41d695f664fdd9346c66
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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