3-Fluoro-5-(trifluoromethyl)benzeneboronic acid → 4-Methyl-2-[4'-chloro-3'-trifluoromethyl-5-(3-fluoro-5-trifluoromethylphenoxy)-biphenyl-3-yl]-pentanoic acid methyl ester
Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:27])[CH:4]([C:9]1[CH:10]=[C:11]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[C:18]([C:23]([F:26])([F:25])[F:24])[CH:17]=2)[CH:12]=[C:13]([OH:15])[CH:14]=1)[CH2:5][CH:6]([CH3:8])[CH3:7].[F:28][C:29]1[CH:30]=[C:31](B(O)O)[CH:32]=[C:33]([C:35]([F:38])([F:37])[F:36])[CH:34]=1>>[CH3:1][O:2][C:3](=[O:27])[CH:4]([C:9]1[CH:10]=[C:11]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[C:18]([C:23]([F:26])([F:24])[F:25])[CH:17]=2)[CH:12]=[C:13]([O:15][C:31]2[CH:32]=[C:33]([C:35]([F:37])([F:36])[F:38])[CH:34]=[C:29]([F:28])[CH:30]=2)[CH:14]=1)[CH2:5][CH:6]([CH3:8])[CH3:7]Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The title compound was prepared in 50% yield from 2-(5-hydroxy-4′-chloro-3′-trifluoromethyl-biphenyl-3-yl)-4-methyl-pentanoic acid methyl ester (prepared in Example A) and 3-fluoro-5-trifluoromethylphenylboronic acid under the conditions described in Example 15, step (g).
Quellen und Nachweise
- ORD-Eintrag
- ord-6b7fe30481664814b931d551f4724cb2
- Quelldatensatz
- uspto-grants-2009_07
- Patentnummer
- US07557244B2
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