Benzyl Bromide → HCID 66765436, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:25])[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[C:21]([F:24])([F:23])[F:22])[CH:5]=1.[CH2:26](Br)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH3:1][O:2][C:3](=[O:25])[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]([CH2:26][C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C:12]=2[C:21]([F:24])([F:23])[F: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-trifluoromethyl-1H-indol-3-ylsulfanyl)-benzoic acid methyl ester and benzyl bromide.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-b82d828a252448819c2dfb44b3a31a6c
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09000025B2
Reaction notes
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