1-Bromo-3-fluorobenzene → {4-[1-(3-Bromo-phenyl)-1H-indol-5-yloxy]-butyl}-diethyl-amine
Reaction equation
[CH2:1]([N:3]([CH2:18][CH3:19])[CH2:4][CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][CH:13]=[CH:12]2)[CH3:2].[Br:20][C:21]1[CH:26]=[CH:25][CH:24]=[C:23](F)[CH:22]=1>>[Br:20][C:21]1[CH:22]=[C:23]([N:14]2[C:15]3[C:11](=[CH:10][C:9]([O:8][CH2:7][CH2:6][CH2:5][CH2:4][N:3]([CH2:1][CH3:2])[CH2:18][CH3:19])=[CH:17][CH:16]=3)[CH:12]=[CH:13]2)[CH:24]=[CH:25][CH:26]=1Participants
3
Procedure
In analogy to example 4.6, Diethyl-[4-(1H-indol-5-yloxy)-butyl]-amine and 1-bromo-3-fluoro-benzene were converted to yield {4-[1-(3-Bromo-phenyl)-1H-indol-5-yloxy]-butyl}-diethyl-amine as light yellow oil, MS: 415 (MH+, 1Br).
Sources & evidence
- ORD record
- ord-aad29f079fe147008724b1ef7f46ebe8
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06503907B2
Reaction notes
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