4-Bromo-3,5-dimethyl-1,2-oxazole → 2-Chloro-4-(3,5-dimethyl-isoxazol-4-yl)-pyridine
Reaction equation
Br[C:2]1[C:3]([CH3:8])=[N:4][O:5][C:6]=1[CH3:7].[Cl:9][C:10]1[CH:15]=[C:14](C2C=NN(C3CCCCO3)C=2)[CH:13]=[CH:12][N:11]=1>>[Cl:9][C:10]1[CH:15]=[C:14]([C:2]2[C:3]([CH3:8])=[N:4][O:5][C:6]=2[CH3:7])[CH:13]=[CH:12][N:11]=1Participants
3
Procedure
The title compound was prepared from 4-bromo-3,5-dimethylisoxazole generally according to the synthetic procedure described for 2-Chloro-4-[1-(tetrahydro-pyran-2-yl)-1H-pyrazol-4-yl]-pyridine. HPLC (Rt)=0.81 min (method N)
Workup
- customHPLC (Rt)=0.81 min (method N)
Sources & evidence
- ORD record
- ord-c0508a5dcc9945de9147310e74c962ad
- Source dataset
- uspto-grants-2015_01
- Patent number
- USRE045323E1
Reaction notes
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