3,4-Dimethoxyaniline → HCID 69507257, compound
Reaction equation
[O:1]=[C:2]1[C:10](=[C:11]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:12](O)=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[NH:3]1.[CH3:21][O:22][C:23]1[CH:24]=[C:25]([CH:27]=[CH:28][C:29]=1[O:30][CH3:31])[NH2:26]>>[CH3:21][O:22][C:23]1[CH:24]=[C:25]([NH:26][C:12](=[O:13])[C:11](=[C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[NH:3][C:2]2=[O:1])[C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:27]=[CH:28][C:29]=1[O:30][CH3:31]Participants
3
Procedure
(2-Oxo-1,2-dihydro-indol-3-ylidene)-phenyl-acetic acid (85 mg) was reacted with 3,4-dimethoxyaniline (110 mg) using method B to give 10 mg (8%) of the title compound.
Sources & evidence
- ORD record
- ord-a469d52a5a7d4890a370cc6cd3fdc919
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07214700B2
Reaction notes
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