Reaktionsgleichung
C(OC(N1CC=C(B2OC(C)(C)C(C)(C)O2)CC1)=O)(C)(C)C.[C:23]([O:27][C:28]([N:30]1[CH2:35][CH:34]=[C:33]([C:36]2[CH:41]=[CH:40][C:39]([C:42]3[N:47]=[CH:46][CH:45]=[CH:44][N:43]=3)=[CH:38][C:37]=2[F:48])[CH2:32][CH2:31]1)=[O:29])([CH3:26])([CH3:25])[CH3:24].BrC1C=C([F:56])C(Br)=CC=1F>>[C:23]([O:27][C:28]([N:30]1[CH2:31][CH:32]=[C:33]([C:36]2[CH:41]=[C:40]([F:56])[C:39]([C:42]3[N:47]=[CH:46][CH:45]=[CH:44][N:43]=3)=[CH:38][C:37]=2[F:48])[CH2:34][CH2:35]1)=[O:29])([CH3:26])([CH3:24])[CH3:25]Komponenten
4
Versuchsvorschrift
The Compound 12AQ was prepared from 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester using the procedure as described for the preparation of Compound 4-(2-fluoro-4-pyrimidin-2-yl-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester but using 1,4-dibromo-2,5-difluoro-benzene in place of 4-bromo-2-fluoro-1-iodobenzene.
Quellen und Nachweise
- ORD-Eintrag
- ord-7d7254c9706745ea8d855bf3186370e5
- Quelldatensatz
- uspto-grants-2013_10
- Patentnummer
- US08546404B2
Verknüpfte Notizen
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