3-Bromo-5-methoxypyridine → HCID 66701425, compound
Reaction equation
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1.[CH2:10]([C:12]1[CH:17]=[CH:16][C:15](B(O)O)=[CH:14][CH:13]=1)[CH3:11]>>[CH2:10]([C:12]1[CH:17]=[CH:16][C:15]([C:2]2[CH:3]=[N:4][CH:5]=[C:6]([O:8][CH3:9])[CH:7]=2)=[CH:14][CH:13]=1)[CH3:11]Participants
3
Procedure
5.0 g (27 mmol) of 3-bromo-5-methoxypyridine and 4.8 g (32 mmol, 1.2 eq.) of 4-ethylphenylboronic acid were reacted according to General Method 1A. Yield: 3.0 g (53% of theory)
Sources & evidence
- ORD record
- ord-23d7e0dbea5845f0a400a64be847f035
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987248B2
Reaction notes
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