HCID 22668401, compound → HCID 178456771, 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][N:25]([CH3:38])[CH2:26][CH2:27][CH2:28][N:29]([CH3:37])[C:30]1[CH:35]=[CH:34][C:33]([NH2:36])=[CH:32][CH:31]=1>>[CH3:38][N:25]([CH3:24])[CH2:26][CH2:27][CH2:28][N:29]([C:30]1[CH:31]=[CH:32][C:33]([NH:36]/[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:34][CH:35]=1)[CH3:37]Participants
3
Procedure
Prepared from 1-acetyl-3-(1-ethoxy-1-ethyl-methylidene)-5,6-dimethoxy-2-indolinone and N-(3-dimethylaminopropyl)-N-methyl-p-phenylenediamine
Sources & evidence
- ORD record
- ord-c576848bc8c6440ca5a38c5a73c72d2b
- Source dataset
- uspto-grants-2004_09
- Patent number
- US06794395B1
Reaction notes
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