5-Fluoro-2-methoxyphenylboronic acid → 2-Chloro-5'-fluoro-2'-methoxybiphenyl-4-yl phenyl sulfone
Reaction equation
[C:1]1([S:7]([C:10]2[CH:15]=[CH:14][C:13](Br)=[C:12]([Cl:17])[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:18][C:19]1[CH:20]=[CH:21][C:22]([O:28][CH3:29])=[C:23](B(O)O)[CH:24]=1>>[C:1]1([S:7]([C:10]2[CH:15]=[CH:14][C:13]([C:21]3[CH:20]=[C:19]([F:18])[CH:24]=[CH:23][C:22]=3[O:28][CH3:29])=[C:12]([Cl:17])[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
The subtitle compound was prepared by the method of example 2 step (ii) using the product of step (i) and 5-fluoro-2-methoxybenzene boronic acid.
Sources & evidence
- ORD record
- ord-ab4479e5214d4b59a121dd70a1f89d0e
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08349897B2
Reaction notes
Loading…