Benzyl Bromide → HCID 66764758, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][CH:19]=1)[O:5][C:6]1[C:14]2[C:9](=[CH:10][C:11]([Cl:15])=[CH:12][CH:13]=2)[NH:8][C:7]=1[CH3:16].[CH2:20](Br)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[CH2:20]([N:8]1[C:9]2[C:14](=[CH:13][CH:12]=[C:11]([Cl:15])[CH:10]=2)[C:6]([O:5][C:4]2[CH:17]=[CH:18][CH:19]=[C:2]([Br:1])[CH:3]=2)=[C:7]1[CH3:16])[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1Participants
3
Procedure
Prepared according to the procedure described in Example 4, Step 1, using the following starting materials: 3-(3-bromo-phenoxy)-6-chloro-2-methyl-1H-indole and benzyl bromide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-1a1cdaac77bd46acb185cb1a0b345e53
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000025B2
Reaction notes
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