Benzyl Bromide → HCID 86615268, compound
Reaction equation
[C:1]([O:5][C:6](=[O:28])[N:7]([C:16]1[N:17]=[C:18]([Cl:27])[CH:19]=[C:20]2[C:24]([CH3:25])=[C:23]([CH3:26])[NH:22][C:21]=12)[CH2:8][C:9]1[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[CH2:29](Br)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>>[C:1]([O:5][C:6](=[O:28])[N:7]([C:16]1[N:17]=[C:18]([Cl:27])[CH:19]=[C:20]2[C:24]([CH3:25])=[C:23]([CH3:26])[N:22]([CH2:29][C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C:21]=12)[CH2:8][C:9]1[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=1)([CH3:4])([CH3:2])[CH3:3]Participants
3
Procedure
In accordance with the same procedures as in Example 657, except for using (5-chloro-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-(4-fluorobenzyl)-carbamic acid tert-butyl ester prepared in Step 2 and benzyl bromide, the titled compound was obtained as yellow oil. (Yield: 70%)
Sources & evidence
- ORD record
- ord-6faab11bfe7e4bf8b75fa80d8bd79cd1
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662832B2
Reaction notes
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