4-Nitrobenzyl bromide → HCID 15295114, compound
Reaction equation
[F:1][C:2]([F:37])([F:36])[C:3]1[CH:4]=[C:5]([CH:29]=[C:30]([C:32]([F:35])([F:34])[F:33])[CH:31]=1)[CH2:6][CH2:7][C:8]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:11](=[O:20])[N:10]([CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2N)[N:9]=1.[N+:38](C1C=CC(CBr)=CC=1)([O-])=O>>[F:33][C:32]([F:35])([F:34])[C:30]1[CH:29]=[C:5]([CH:4]=[C:3]([C:2]([F:1])([F:36])[F:37])[CH:31]=1)[CH2:6][CH2:7][C:8]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:11](=[O:20])[N:10]([CH2:21][C:22]2[CH:23]=[CH:24][C:25]([NH2:38])=[CH:26][CH:27]=2)[N:9]=1Participants
3
Procedure
Prepared as for the compound of Example 3 using p-nitrobenzyl bromide.
Sources & evidence
- ORD record
- ord-07a3fd10229348ff9ffaa8db000009ac
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05710161
Reaction notes
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