1-Bromo-2,6-difluorobenzene → (2-Amino-6-chloro-pyridin-3-yl)-(2,6-difluoro-phenyl)-methanone
Reaction equation
[NH2:1][C:2]1[N:13]=[C:12]([Cl:14])[CH:11]=[CH:10][C:3]=1[C:4](N(OC)C)=[O:5].Br[C:16]1[C:21]([F:22])=[CH:20][CH:19]=[CH:18][C:17]=1[F:23]>>[NH2:1][C:2]1[C:3]([C:4]([C:16]2[C:21]([F:22])=[CH:20][CH:19]=[CH:18][C:17]=2[F:23])=[O:5])=[CH:10][CH:11]=[C:12]([Cl:14])[N:13]=1Participants
3
Procedure
The title compound was prepared from 2-Amino-6-chloro-N-methoxy-N-methyl-nicotinamide (Example 3) and 2-bromo-1,3-difluorobenzene (Aldrich) using the procedure described in Example 7. HRMS, observed: 268.0217, Calcd for M+: 268.0215.
Sources & evidence
- ORD record
- ord-01d5fbb683b94a4b84c9036e8c746f35
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07423051B2
Reaction notes
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