Water → Ethyl 3-(5-(5-chloro-2-formylphenyl)picolinamido)propanoate
Reaktionsgleichung
Br[C:2]1[CH:3]=[CH:4][C:5]([C:8]([NH:10][CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])=[O:9])=[N:6][CH:7]=1.[Cl:18][C:19]1[CH:20]=[CH:21][C:22]([CH:28]=[O:29])=[C:23](B(O)O)[CH:24]=1.C([O-])([O-])=O.[K+].[K+].O>O1CCOCC1.CCOC(C)=O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[Cl:18][C:19]1[CH:24]=[CH:23][C:22]([CH:28]=[O:29])=[C:21]([C:2]2[CH:3]=[CH:4][C:5]([C:8]([NH:10][CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])=[O:9])=[N:6][CH:7]=2)[CH:20]=1Komponenten
8
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 3
Versuchsvorschrift
Ethyl 3-(5-bromopicolinamido)propanoate, prepared as in Example 1, (1.5 g, 5.0 mmol), (5-chloro-2-formylphenyl)boronic acid (1.0 g, 5.5 mmol), Pd(dppf)Cl2 (408 mg, 0.5 mmol), and K2CO3 (1.4 g, 10.0 mmol) were dissolved in 1,4-dioxane (20 mL) and water (5 mL) and heated to 80° C. After 3 h the resulting mixture was cooled to room temperature, diluted with EtOAc washed with water and brine, dried (Na2SO4), dry-packed onto silica gel and purified via column chromatography to yield the title compound.
Aufarbeitung
- washwashed with water and brine
- dry with materialdried (Na2SO4)
- customdry-packed onto silica gel and purified via column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-1bbb569803ff454c905529b3f956555a
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08748624B2
Notizen zur Reaktion
Wird geladen…