Benzyl Bromide → HCID 18512216, compound
Reaction equation
[CH2:1]([O:4][C:5]1[CH:29]=[CH:28][C:8]([O:9][C:10]2[CH:27]=[CH:26][C:13]([CH2:14][NH:15][C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([N+:22]([O-:24])=[O:23])[C:17]=3[CH3:25])=[CH:12][CH:11]=2)=[CH:7][CH:6]=1)[CH:2]=[CH2:3].[CH2:30](Br)[C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1>>[CH2:1]([O:4][C:5]1[CH:29]=[CH:28][C:8]([O:9][C:10]2[CH:11]=[CH:12][C:13]([CH2:14][N:15]([CH2:30][C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)[C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([N+:22]([O-:24])=[O:23])[C:17]=3[CH3:25])=[CH:26][CH:27]=2)=[CH:7][CH:6]=1)[CH:2]=[CH2:3]Participants
3
Procedure
The product from Example 60C and benzyl bromide was processed as described in Example 6B to provide the title compound.
Sources & evidence
- ORD record
- ord-24a4deb841454907bb1d7b1ad7d22222
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
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