Benzyl Bromide → HCID 18512093, compound
Reaction equation
[Br:1][C:2]1[CH:26]=[CH:25][C:5]([O:6][C:7]2[CH:24]=[CH:23][C:10]([CH2:11][NH:12][C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-:21])=[O:20])[C:14]=3[CH3:22])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.[CH2:27](Br)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[CH2:27]([N:12]([CH2:11][C:10]1[CH:23]=[CH:24][C:7]([O:6][C:5]2[CH:25]=[CH:26][C:2]([Br:1])=[CH:3][CH:4]=2)=[CH:8][CH:9]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([N+:19]([O-:21])=[O:20])[C:14]=1[CH3:22])[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1Participants
3
Procedure
The product from Example 64B and benzyl bromide were processed as described in Example 6B to provide the title compound.
Sources & evidence
- ORD record
- ord-e08c0f18fb7c40c7825f44a8a206621b
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
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