Benzyl Bromide → HCID 86753763, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7]([C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=1)=[C:6]2[CH2:19][C:20]([O:22][CH3:23])=[O:21].[CH2:24](Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[N:8]([CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[C:7]([C:12]1[CH:13]=[CH:14][C:15]([F:18])=[CH:16][CH:17]=1)=[C:6]2[CH2:19][C:20]([O:22][CH3:23])=[O:21]Participants
3
Procedure
Prepare by a method similar to Example 48 using methyl [5-methoxy-2-(4-fluorophenyl)-indol-3-yl]-acetate and benzyl bromide.
Sources & evidence
- ORD record
- ord-8d2a50f04c9348e696dc0b552c57ed0c
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05877202
Reaction notes
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