Tolylboronic acid → HCID 22240225, compound
Reaction equation
B(O)(O)[C:2]1[CH:3]=[CH:4][C:5]([CH3:8])=[CH:6][CH:7]=1.[Cl:11][C:12]1[CH:13]=[C:14]([CH2:18][N:19]2[CH:23]=[CH:22][N:21]=[C:20]2[CH3:24])[N:15]=[N:16][CH:17]=1>>[ClH:11].[CH3:24][C:20]1[N:19]([CH2:18][C:14]2[N:15]=[N:16][CH:17]=[C:12]([C:2]3[CH:3]=[CH:4][C:5]([CH3:8])=[CH:6][CH:7]=3)[CH:13]=2)[CH:23]=[CH:22][N:21]=1Participants
3
Procedure
The title compound, MS: m/e=265.3 (M+H+), was prepared from p-tolylboronic acid and 5-chloro-3-(2-methyl-imidazol-1-yl-methyl)-pyridazine.
Sources & evidence
- ORD record
- ord-6cb7b6082d0d4cbca926430e85653af6
- Source dataset
- uspto-grants-2006_02
- Patent number
- US07005432B2
Reaction notes
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