HCID 22668401, compound → HCID 178468597, compound

HRID 1883785Notes

Reaction equation

HRID 1883785 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.[CH3:29][N:30]([CH3:43])[CH2:31][CH2:32][CH2:33][N:34]([C:36]1[CH:42]=[CH:41][C:39]([NH2:40])=[CH:38][CH:37]=1)[CH3:35]>>[CH3:43][N:30]([CH3:29])[CH2:31][CH2:32][CH2:33][N:34]([C:36]1[CH:37]=[CH:38][C:39]([NH:40]/[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:41][CH:42]=1)[CH3:35]

Participants

3

Procedure

Prepared from 1-acetyl-3-(1-ethoxy-1-phenylmethylene)-6-ethoxycarbonyl-2-indolinone and 4-(N-(3-dimethylamino-propyl)-N-methyl-amino)-aniline Rf value: 0.5 (aluminium oxide, ethyl acetate) C30H34N4O3

Sources & evidence

ORD record
ord-fc3d14b49e4740929daddd7f08dae879
Source dataset
uspto-grants-2004_07
Patent number
US06762180B1

Reaction notes

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