Benzyl Bromide → HCID 118558033, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[C:8](=[O:14])/[C:7](=[CH:15]/[C:16]1[CH:21]=[CH:20][N:19]=[CH:18][C:17]=1[C:22]([O:24][CH3:25])=[O:23])/[CH2:6]2.[CH2:26]([Br:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[Br-:33].[CH2:26]([N+:19]1[CH:20]=[CH:21][C:16](/[CH:15]=[C:7]2/[C:8](=[O:14])[C:9]3[C:5]([CH2:6]/2)=[CH:4][C:3]([O:2][CH3:1])=[C:11]([O:12][CH3:13])[CH:10]=3)=[C:17]([C:22]([O:24][CH3:25])=[O:23])[CH:18]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1Participants
3
Procedure
The title compound 150 is prepared according to the procedure reported in Example 38.1 with compound 96 (34 mg, 0.10 mmol) and benzyl bromide (25 μL, 0.21 mmol) as reactants. White solid. (Yield 46.1 mg, 90%).
Sources & evidence
- ORD record
- ord-5f13ec7f4a28456d816f618e163a1ec1
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09376387B2
Reaction notes
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