4-[4-(4-fluorophenyl)-5-(2-pyridyl)-1H-imidazol-2yl]benzonitrile → 4-[4-(4-Fluorophenyl)-5-(2-pyridyl)-1H-imidazol-2-yl]benzoic acid
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([C:19]3[CH:27]=[CH:26][C:22]([C:23]([OH:25])=[O:24])=[CH:21][CH:20]=3)[NH:11][C:12]=2C2C=CN=CC=2)=[CH:4][CH:3]=1.FC1C=CC(C2N=C(C3C=CC(C#N)=CC=3)NC=2[C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][N:41]=2)=CC=1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[N:9]=[C:10]([C:19]3[CH:20]=[CH:21][C:22]([C:23]([OH:25])=[O:24])=[CH:26][CH:27]=3)[NH:11][C:12]=2[C:40]2[CH:45]=[CH:44][CH:43]=[CH:42][N:41]=2)=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared using the procedure in U.S. Pat. No. 5,656,644 (Example 9) to prepare 4- [4-(4-fluorophenyl)-5-(4-pyridyl)-1H-imidazol-2yl]benzoic acid except using 4-[4-(4-fluorophenyl)-5-(2-pyridyl)-1H-imidazol-2yl]benzonitrile. ESMS (M+H)+=360.1.
Sources & evidence
- ORD record
- ord-a44e6e2d03594edc893844bdc7395679
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06465493B1
Reaction notes
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