1,1'-Biphenyl-4-yl-boronic acid → HCID 22240214, compound
Reaction equation
[C:1]1([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:6]=[CH:5][C:4](B(O)O)=[CH:3][CH:2]=1.[Cl:16][C:17]1[CH:18]=[C:19]([CH2:23][N:24]2[CH:28]=[CH:27][N:26]=[C:25]2[CH3:29])[N:20]=[N:21][CH:22]=1>>[ClH:16].[C:1]1([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:6]=[CH:5][C:4]([C:17]2[CH:18]=[C:19]([CH2:23][N:24]3[CH:28]=[CH:27][N:26]=[C:25]3[CH3:29])[N:20]=[N:21][CH:22]=2)=[CH:3][CH:2]=1Participants
3
Procedure
The title compound, MS: m/e=327.4 (M+H+), was prepared from 4-biphenylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.
Sources & evidence
- ORD record
- ord-ea7d1fda760a4a94a84b5d41ca5fd404
- Source dataset
- uspto-grants-2006_02
- Patent number
- US07005432B2
Reaction notes
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