(2,3-Difluorophenyl)boronic acid → (2-Dimethylamino-2',3'-difluoro-5-nitro-biphenyl-4-yl)-carbamic acid tert.-butyl ester
Reaktionsgleichung
[C:1]([O:5][C:6](=[O:21])[NH:7][C:8]1[CH:13]=[C:12]([N:14]([CH3:16])[CH3:15])[C:11](I)=[CH:10][C:9]=1[N+:18]([O-:20])=[O:19])([CH3:4])([CH3:3])[CH3:2].[F:22][C:23]1[C:28]([F:29])=[CH:27][CH:26]=[CH:25][C:24]=1B(O)O>>[C:1]([O:5][C:6](=[O:21])[NH:7][C:8]1[C:9]([N+:18]([O-:20])=[O:19])=[CH:10][C:11]([C:27]2[CH:26]=[CH:25][CH:24]=[C:23]([F:22])[C:28]=2[F:29])=[C:12]([N:14]([CH3:16])[CH3:15])[CH:13]=1)([CH3:4])([CH3:3])[CH3:2]Komponenten
3
Versuchsvorschrift
The title compound was prepared from (5-dimethylamino-4-iodo-2-nitro-phenyl)-carbamic acid tert.-butyl ester (Example C2) and 2,3-difluorophenylboronic acid according to the general procedure D. Obtained as a yellow solid (3.096 g).
Quellen und Nachweise
- ORD-Eintrag
- ord-6750199ccbe149c8aa879f7a016c9b5a
- Quelldatensatz
- uspto-grants-2003_04
- Patentnummer
- US06544985B2
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