(Oxan-4-yl)methanol → 5-bromo-3-fluoro-2-((4-fluorotetrahydro-2H-pyran-4-yl)methoxy)pyridine
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([CH2:7][OH:8])[CH2:3][CH2:2]1.[Br:9][C:10]1[CH:11]=[C:12]([F:17])[C:13](F)=[N:14][CH:15]=1.[F:18]C1C=CC(S(N)(=O)=O)=CC=1[N+]([O-])=O>>[Br:9][C:10]1[CH:11]=[C:12]([F:17])[C:13]([O:8][CH2:7][C:4]2([F:18])[CH2:5][CH2:6][O:1][CH2:2][CH2:3]2)=[N:14][CH:15]=1Participants
4
Procedure
The title compound was prepared by substituting EXAMPLE 306C for (tetrahydro-2H-pyran-4-yl)methanol and 5-bromo-2,3-difluoropyridine for 4-fluoro-3-nitrobenzenesulfonamide in EXAMPLE 279A.
Sources & evidence
- ORD record
- ord-788a1f51ac824582bf3fff2c8c391c65
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09315488B2
Reaction notes
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