Boron tribromide → HCID 59651990, compound
Reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:14]([CH3:15])=[N:13][N:12]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=3)[C:11](=[O:22])[CH:10]=2)=[CH:5][CH:4]=1.B(Br)(Br)Br>C(Cl)Cl>[OH:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:14]([CH3:15])=[N:13][N:12]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=3)[C:11](=[O:22])[CH:10]=2)=[CH:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5-(4-Hydroxy-phenyl)-6-methyl-2-pyridin-2-yl-2H-pyridazin-3-one was prepared from 5-(4-Methoxy-phenyl)-6-methyl-2-pyridin-2-yl-2H-pyridazin-3-one and BBr3 in CH2Cl2 using the procedure described in Example 91 Step 3; Mp 252-4° C.; MS m/z 280 (M+H).
Sources & evidence
- ORD record
- ord-7ec235655d4543838db4c23ba347e875
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247414B2
Reaction notes
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