1,4-Dioxane → {2-ethyl-8-fluoro-4-oxo-3-[4-(pyrrolidine-1-carbonyl)benzyl]-1,4-dihydroquinolin-5-yloxy}acetic Acid Methyl Ester
Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:14])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[C:8]([NH2:13])[CH:7]=1.C[O:16][C:17](=O)[CH:18]([CH2:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]([N:32]2[CH2:36][CH2:35][CH2:34][CH2:33]2)=[O:31])=[CH:26][CH:25]=1)[C:19](=O)[CH2:20][CH3:21].O1CCOCC1>O>[CH3:1][O:2][C:3](=[O:14])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([F:12])=[C:8]2[C:7]=1[C:17](=[O:16])[C:18]([CH2:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]([N:32]3[CH2:33][CH2:34][CH2:35][CH2:36]3)=[O:31])=[CH:26][CH:25]=1)=[C:19]([CH2:20][CH3:21])[NH:13]2Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 120 °C
Versuchsvorschrift
A mixture of (3-amino-4-fluorophenoxy)acetic acid methyl ester (0.39 g), 3-oxo-2-[4-(pyrrolidine-1-carbonyl)benzyl]pentanoic acid methyl ester (1.0 g), polyphosphoric acid (2 g) and dioxane (20 mL) was heated at 120° C. for 18 hours. The mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The combined extracts were dried over magnesium sulfate and the solvent removed under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with a mixture of dichloromethane and methanol (9:1 by volume) to afford title compound, 0.25 g.
Aufarbeitung
- temperatureThe mixture was cooled to room temperature
- extractionextracted with ethyl acetate
- dry with materialThe combined extracts were dried over magnesium sulfate
- customthe solvent removed under reduced pressure
- customThe residue was purified by column chromatography on silica gel
- washeluting with a mixture of dichloromethane and methanol (9:1 by volume)
Quellen und Nachweise
- ORD-Eintrag
- ord-962b28f711324995981d8c8ec49a90d4
- Quelldatensatz
- uspto-grants-2010_12
- Patentnummer
- US07858640B2
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