Boronic Acid → 5-Pyridin-3-yl-1,2,3,4-tetrahydro-isoquinoline
Reaction equation
Br[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][NH:6][CH2:7]2.B(O)O>>[N:6]1[CH:7]=[CH:8][CH:3]=[C:4]([C:2]2[CH:11]=[CH:10][CH:9]=[C:8]3[C:3]=2[CH2:4][CH2:5][NH:6][CH2:7]3)[CH:5]=1Participants
3
Procedure
In close analogy to the procedure described above, 5-Bromo-1,2,3,4-tetrahydro-isoquinoline is reacted with the corresponding boronic acid to provide the title compound.
Sources & evidence
- ORD record
- ord-9224fdfaeba342f99c5adae8568cff77
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07985753B2
Reaction notes
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