Benzyl Bromide → HCID 66765426, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:20])=[CH:17][CH:18]=3)[NH:13][C:12]=2[CH2:21][CH3:22])[CH:5]=1.[CH2:24](Br)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH3:1][O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][C:11]2[C:19]3[C:14](=[CH:15][C:16]([Cl:20])=[CH:17][CH:18]=3)[N:13]([CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:12]=2[CH2:21][CH3:22])[CH:5]=1Participants
3
Procedure
Prepared according to the procedure described in Example 10, Step 3, using the following starting materials: 3-(6-chloro-2-ethyl-1H-indol-3-ylsulfanyl)-benzoic acid methyl ester and benzyl bromide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-9b70626860eb4cc49d27e612599fdaa8
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000025B2
Reaction notes
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