3-Nitrophenylboronic Acid → HCID 19381188, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]2[CH:9]=[C:10]3[C:15](=[C:16](Br)[CH:17]=2)[N:14]=[CH:13][CH:12]=[CH:11]3)[CH:2]=1.[N+:19]([C:22]1[CH:23]=[C:24](B(O)O)[CH:25]=[CH:26][CH:27]=1)([O-:21])=[O:20]>>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][C:8]2[CH:9]=[C:10]3[C:15](=[C:16]([C:26]4[CH:25]=[CH:24][CH:23]=[C:22]([N+:19]([O-:21])=[O:20])[CH:27]=4)[CH:17]=2)[N:14]=[CH:13][CH:12]=[CH:11]3)[CH:2]=1Participants
3
Procedure
6-(3-pyridylmethyl)-8-bromoquinoline and 3-nitrobenzene boronic acid can be combined to form 6-(3-pyridylmethyl)-8-(3-nitrophenyl)quinoline,
Sources & evidence
- ORD record
- ord-72edaeeaaec14a0ebfbc1f7de2eaf3b7
- Source dataset
- uspto-grants-1995_10
- Patent number
- US05455252
Reaction notes
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