5-Fluoro-2-methoxyphenylboronic acid → HCID 67238697, compound
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)(=[O:10])=[O:9])=[C:4]([C:17]([F:20])([F:19])[F:18])[CH:3]=1.[F:21][C:22]1[CH:23]=[CH:24][C:25]([O:31][CH3:32])=[C:26](B(O)O)[CH:27]=1>>[C:11]1([S:8]([C:5]2[CH:6]=[CH:7][C:2]([C:24]3[CH:23]=[C:22]([F:21])[CH:27]=[CH:26][C:25]=3[O:31][CH3:32])=[CH:3][C:4]=2[C:17]([F:20])([F:19])[F:18])(=[O:10])=[O:9])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=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-62c87fbd2d54425bab9ed3282cad5963
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08415394B2
Reaction notes
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