Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:17])=[C:6]([C@:8]2([CH3:16])[C@@H:13]([F:14])[CH2:12][O:11][C:10]([NH2:15])=[N:9]2)[CH:7]=1.[F:18][C:19]1[C:20]([C:26](O)=[O:27])=[N:21][CH:22]=[C:23]([F:25])[CH:24]=1>>[NH2:15][C:10]1[O:11][CH2:12][C@H:13]([F:14])[C@:8]([C:6]2[CH:7]=[C:2]([NH:1][C:26]([C:20]3[C:19]([F:18])=[CH:24][C:23]([F:25])=[CH:22][N:21]=3)=[O:27])[CH:3]=[CH:4][C:5]=2[F:17])([CH3:16])[N:9]=1Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The condensation of (4R,5R)-4-(5-amino-2-fluoro-phenyl)-5-fluoro-4-methyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine (intermediate A8.2) and 3,5-difluoro-pyridine-2-carboxylic acid (CAS 745784-04-7) following procedure I yielded the title compound as a white solid. MS (ISP): m/z=383.3 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-77f92d78f78d4f7eaf54a8711cf987a7
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08754075B2
Verknüpfte Notizen
Wird geladen…