Potassium Carbonate → N-(5'-Bromo-3'-fluoro-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl)-N-cyclopropyl-4-oxazol-5-yl-benzamide
Reaktionsgleichung
[CH:1]1([N:4]([CH:18]2[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)[C:5](=[O:17])[C:6]2[CH:11]=[CH:10][C:9]([C:12]3[O:16][CH:15]=[N:14][CH:13]=3)=[CH:8][CH:7]=2)[CH2:3][CH2:2]1.[Br:24][C:25]1[CH:26]=[C:27]([F:32])[C:28](F)=[N:29][CH:30]=1.C([O-])([O-])=O.[K+].[K+]>CN1CCCC1=O>[Br:24][C:25]1[CH:26]=[C:27]([F:32])[C:28]([N:21]2[CH2:22][CH2:23][CH:18]([N:4]([CH:1]3[CH2:3][CH2:2]3)[C:5](=[O:17])[C:6]3[CH:7]=[CH:8][C:9]([C:12]4[O:16][CH:15]=[N:14][CH:13]=4)=[CH:10][CH:11]=3)[CH2:19][CH2:20]2)=[N:29][CH:30]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The title compound is prepared from N-Cyclopropyl-4-oxazol-5-yl-N-piperidin-4-yl-benzamide and 5-bromo-2,3-difluoro-pyridine following a procedure analogous to that described in Example 61 using K2CO3 as base and N-methylpyrrolidinone as solvent. LC (method 1): tR=1.35 min; Mass spectrum (ESI+): m/z=507 [M+Na]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-8c16364015134bdeb4777619505b92c1
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08822471B2
Notizen zur Reaktion
Wird geladen…