HCID 23507706, compound → HCID 178444773, compound
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH3:16])=[O:14])[CH:11]=2)[C:6](=[C:17](OCC)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:5]1=[O:27])(=O)C.[CH2:28]([N:34]([CH2:36][C:37]1[CH:43]=[CH:42][C:40]([NH2:41])=[CH:39][CH:38]=1)[CH3:35])[CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]>>[CH2:28]([N:34]([CH2:36][C:37]1[CH:43]=[CH:42][C:40]([NH:41]/[C:17](=[C:6]2\[C:5](=[O:27])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[C:10]([C:13]([O:15][CH3:16])=[O:14])[CH:11]=3)/[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:39][CH:38]=1)[CH3:35])[CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-phenylmethylene)-6-methoxycarbonyl-2-indolinone and 4-(N-(n-hexyl)-N-methyl-aminomethyl)-aniline Rf value: 0.6 (silica gel, methylene chloride/methanol=10:1) C31H35N3O3
Sources & evidence
- ORD record
- ord-b8e60299934b4dfb8ead6de1d61cd672
- Source dataset
- uspto-grants-2004_07
- Patent number
- US06762180B1
Reaction notes
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