7-Methylindole-3-carboxaldehyde → HCID 178423648, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[CH3:10][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:19]=1[NH:18][CH:17]=[C:16]2[CH:20]=O>>[Br:1][C:2]1[CH:3]=[C:4]2[N:9]=[C:20]([C:16]3[C:15]4[C:19](=[C:11]([CH3:10])[CH:12]=[CH:13][CH:14]=4)[NH:18][CH:17]=3)[NH:8][C:5]2=[N:6][CH:7]=1Participants
3
Procedure
The title compound was prepared from 5-bromo-2,3-diaminopyridine and 7-methylindole-3-carboxaldehyde.
Sources & evidence
- ORD record
- ord-552a47e8313c4947bc271fcddf745762
- Source dataset
- uspto-grants-2008_08
- Patent number
- US07410966B2
Reaction notes
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