5-Chloro-2-methoxyphenylboronic acid → 5'-Chloro-3,5-difluoro-2'-methoxybiphenyl-4-yl phenyl sulfone
Reaction equation
[C:1]1([S:7]([C:10]2[C:15]([F:16])=[CH:14][C:13](Br)=[CH:12][C:11]=2[F:18])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:19][C:20]1[CH:21]=[CH:22][C:23]([O:29][CH3:30])=[C:24](B(O)O)[CH:25]=1>>[C:1]1([S:7]([C:10]2[C:15]([F:16])=[CH:14][C:13]([C:22]3[CH:21]=[C:20]([Cl:19])[CH:25]=[CH:24][C:23]=3[O:29][CH3:30])=[CH:12][C:11]=2[F:18])(=[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-chloro-2-methoxybenzene boronic acid which was used directly in step (iv) without further characterisation.
Sources & evidence
- ORD record
- ord-e5e1ff3ec91e4a79b1f80c249e7ff5fd
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415394B2
Reaction notes
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