Benzyl Bromide → HCID 118558061, compound
Reaction equation
[F:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[CH2:8][CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:19][CH3:20])[CH:15]=2)[C:10]1=[O:23].[CH2:24]([Br:31])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[Br-:31].[CH2:24]([N+:4]1[CH:5]=[CH:6][C:7]([CH2:8][CH:9]2[CH2:18][CH2:17][C:16]3[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:19][CH3:20])[CH:15]=3)[C:10]2=[O:23])=[C:2]([F:1])[CH:3]=1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1Participants
3
Procedure
The title compound 133 is prepared according to the procedure reported in Example 38.1 with compound 102 (135.8 mg, 0.43 mmol) and benzyl bromide (87 μL, 0.73 mmol) as reactants. White solid. (Yield 152.1 mg, 72%).
Sources & evidence
- ORD record
- ord-a4fa609cf49846f5926f23f5ec5fd8aa
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376387B2
Reaction notes
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