2-Chloro-5-hydroxypyridine → 6-[4-(Trifluoromethyl)phenyl]pyridin-3-ol
Reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[F:9][C:10]([F:21])([F:20])[C:11]1[CH:16]=[CH:15][C:14](B(O)O)=[CH:13][CH:12]=1>>[F:9][C:10]([F:21])([F:20])[C:11]1[CH:16]=[CH:15][C:14]([C:2]2[N:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=2)=[CH:13][CH:12]=1Participants
3
Procedure
The titled compound is made in a manner substantially similar to Preparation 28 starting from the 6-chloro-pyridin-3-ol and 4-trifluoromethylphenyl boronic acid.
Sources & evidence
- ORD record
- ord-2e71052737394b5eb0cd136febf453cb
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084489B2
Reaction notes
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