3,5-Difluoropyridine-2-carboxylic acid → HCID 53241712, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:18])=[C:6]([C@:8]2([CH3:17])[C:13]([F:15])([F:14])[CH2:12][O:11][C:10]([NH2:16])=[N:9]2)[CH:7]=1.[F:19][C:20]1[C:21]([C:27](O)=[O:28])=[N:22][CH:23]=[C:24]([F:26])[CH:25]=1>>[NH2:16][C:10]1[O:11][CH2:12][C:13]([F:14])([F:15])[C@:8]([C:6]2[CH:7]=[C:2]([NH:1][C:27]([C:21]3[C:20]([F:19])=[CH:25][C:24]([F:26])=[CH:23][N:22]=3)=[O:28])[CH:3]=[CH:4][C:5]=2[F:18])([CH3:17])[N:9]=1Komponenten
3
Versuchsvorschrift
The condensation of (R)-4-(5-amino-2-fluoro-phenyl)-5,5-difluoro-4-methyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine (intermediate XI-1) and 3,5-difluoro-pyridine-2-carboxylic acid following procedure I yielded the title compound as a colorless solid. MS (ISP): m/z=401.2 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-558483167cd748f7b3e323de555f563f
- Quelldatensatz
- uspto-grants-2013_03
- Patentnummer
- US08389513B2
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