5-Aminoindole → HCID 11266848, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]([OH:11])=O)=[CH:7][C:6]([C:12]([NH2:14])=[O:13])=[CH:5][CH:4]=1.[NH2:15][C:16]1[CH:17]=[C:18]2[C:22](=[CH:23][CH:24]=1)[NH:21][CH:20]=[CH:19]2>>[NH:21]1[C:22]2[C:18](=[CH:17][C:16]([NH:15][C:9](=[O:11])[C:8]3[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=3[O:2][CH3:1])[C:12]([NH2:14])=[O:13])=[CH:24][CH:23]=2)[CH:19]=[CH:20]1Participants
3
Procedure
The captioned compound was synthesized from 6-methoxyisophthalamic acid and 5-aminoindole by the same procedure as in the manufacturing method described in step C of Example 1-3-1.
Sources & evidence
- ORD record
- ord-fa4ed8b4973e44da921290c4021834b2
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07705053B2
Reaction notes
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