Benzyl Bromide → HCID 59762346, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:14]2[C:9](=[CH:10][C:11]([N+:16]([O-:18])=[O:17])=[C:12]([F:15])[CH:13]=2)[NH:8][C:7]=1[CH:19]([CH3:21])[CH3:20])=[O:5])[CH3:2].[CH2:22](Br)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[CH2:22]([N:8]1[C:9]2[C:14](=[CH:13][C:12]([F:15])=[C:11]([N+:16]([O-:18])=[O:17])[CH:10]=2)[C:6]([C:4]([O:3][CH2:1][CH3:2])=[O:5])=[C:7]1[CH:19]([CH3:20])[CH3:21])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
3
Procedure
The title compound was prepared from ethyl5-fluoro-2-isopropyl-6-nitro-1H-indole-3-carboxylate (Compound 168) and benzyl bromide by General Procedure J.
Sources & evidence
- ORD record
- ord-c5926f83dae44f278189c0d69924e5eb
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08524917B2
Reaction notes
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