Reaction equation
Br[C:2]1[N:7]=[CH:6][C:5]([NH2:8])=[CH:4][CH:3]=1.[F:9][C:10]1[CH:11]=[N:12][CH:13]=[C:14]([F:29])[C:15]=1[Sn](CCCC)(CCCC)CCCC>>[F:9][C:10]1[CH:11]=[N:12][CH:13]=[C:14]([F:29])[C:15]=1[C:2]1[CH:3]=[CH:4][C:5]([NH2:8])=[CH:6][N:7]=1Participants
3
Procedure
Obtained (50% yield) following the procedure described in example 34 (step A), starting with 6-bromopyridin-3-amine and 3,5-difluoro-4-(tributylstannyl)pyridine.
Workup
- customObtained (50% yield)
Sources & evidence
- ORD record
- ord-c4a5c136a52f45c5a1055d3fd4a0e082
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08536165B2
Linked notes
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