5-Bromo-2-nitroanisole → 5-bromo-7-methoxy-1H-indole
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N+:10]([O-])=O)=[C:6]([O:8][CH3:9])[CH:7]=1.Br[C:14]1C=CC(OC)=C2[C:15]=1C=CN2>>[Br:1][C:2]1[CH:3]=[C:4]2[C:5](=[C:6]([O:8][CH3:9])[CH:7]=1)[NH:10][CH:15]=[CH:14]2Participants
3
Procedure
5-Bromo-7-methoxyindole CV was prepared from 5-bromo-2-nitroanisole using the procedure described above for preparation of 4-bromo-7-methoxyindole LII (Example 13).
Sources & evidence
- ORD record
- ord-76dbb4d6429e4d56864d2066f7f64ac3
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07803830B2
Reaction notes
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