4-Chloro-3-hydroxyphenylacetic acid → {4-Chloro-3-[2-fluoro-4-(phenylsulfonyl)phenoxy]phenyl}acetic acid
Reaction equation
[C:1]1([S:7]([C:10]2[CH:15]=[CH:14][C:13](F)=[C:12]([F:17])[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([OH:28])=[O:27])=[CH:21][C:20]=1[OH:29]>>[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([OH:28])=[O:27])=[CH:21][C:20]=1[O:29][C:13]1[CH:14]=[CH:15][C:10]([S:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)(=[O:9])=[O:8])=[CH:11][C:12]=1[F:17]Participants
3
Procedure
The title compound was prepared by the method of example 2 step (iii) using the product of step (i) and the product of example 1 step (iii).
Sources & evidence
- ORD record
- ord-775d55721c04413e9490448a4a3df3fa
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148572B2
Reaction notes
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