5-Bromo-2-iodotoluene → 3-(4-Bromo-2-methyl-phenyl)-5-fluoro-pyridine
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5](I)=[C:6]([CH3:8])[CH:7]=1.[F:10][C:11]1[CH:12]=[C:13](B(O)O)[CH:14]=[N:15][CH:16]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:13]2[CH:14]=[N:15][CH:16]=[C:11]([F:10])[CH:12]=2)=[C:6]([CH3:8])[CH:7]=1Participants
3
Procedure
The title compound was prepared from 5-bromo-2-iodotoluene and 5-fluoropyridine-3-boronic acid in analogy to Example 1b): MS (ISP): 265.8 and 267.9 (M+H)+.
Sources & evidence
- ORD record
- ord-6fd71ae0629f40fcba69883a937a761d
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367838B2
Reaction notes
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