3-Bromopyridine → HCID 53016961, compound
Reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[F:8][C:9]([F:19])([F:18])[C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=1.N1C=CC=CC=1C=O>>[N:4]1[CH:5]=[CH:6][CH:7]=[C:2]([CH:14]([C:13]2[CH:12]=[CH:11][C:10]([C:9]([F:8])([F:18])[F:19])=[CH:17][CH:16]=2)[OH:15])[CH:3]=1Participants
4
Procedure
The title compound was prepared analogously to the method in Intermediate 25: step a using 3-bromopyridine and 4-(trifluoromethyl)benzaldehyde in place of 5-bromo-1-methyl-1H-imidazole and picolinaldehyde, respectively.
Sources & evidence
- ORD record
- ord-b200a348e17244289b68764abfc22ddc
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290476B2
Reaction notes
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