Benzyl Bromide → HCID 66765142, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([C:14]=1[S:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([Br:22])[CH:17]=1)=[CH:12][CH:11]=[C:10]([Cl:23])[CH:9]=2)=[O:5])[CH3:2].[CH2:24](Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[C:8]2[C:13]([C:14]=1[S:15][C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([Br:22])[CH:17]=1)=[CH:12][CH:11]=[C:10]([Cl:23])[CH:9]=2)=[O:5])[CH3:2]Participants
3
Procedure
Prepared according to the procedure described in Example 4, Step 1, using the following starting materials: 3-(3-bromo-phenylsulfanyl)-6-chloro-1H-indole-2-carboxylic acid ethyl ester and benzyl bromide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-7a0d1b7dd17445fe857a9f0e9c823596
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000025B2
Reaction notes
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