3-Methoxyaniline → (3Z)-3-[(3-methoxyanilino)-phenylmethylidene]-1H-indol-2-one
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=[C:13](Cl)[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]1=[O:21])(=O)C.[CH3:22][O:23][C:24]1[CH:25]=[C:26]([CH:28]=[CH:29][CH:30]=1)[NH2:27].[OH-].[Na+]>C1COCC1>[CH3:22][O:23][C:24]1[CH:25]=[C:26]([NH:27]/[C:13](=[C:6]2\[C:5](=[O:21])[NH:4][C:12]3[C:7]\2=[CH:8][CH:9]=[CH:10][CH:11]=3)/[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)[CH:28]=[CH:29][CH:30]=1Participants
5
Procedure
Prepared analogously to Example 2 from 1-acetyl-3-(1-chloro-1-phenyl-methylidene)-2-indolinone and 3-methoxyaniline in THF and subsequent treatment with sodium hydroxide solution.
Sources & evidence
- ORD record
- ord-318a4454c4ab4a2498939cde2b72a4cc
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855710B2
Reaction notes
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