Reaktionsgleichung
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][N:9]=2)[CH:4]=[CH:3][C:2]=1O.P(Cl)(Cl)([Cl:14])=O>>[Cl:14][C:2]1[CH:3]=[CH:4][C:5]2[C:10](=[N:9][CH:8]=[CH:7][CH:6]=2)[N:1]=1Komponenten
3
Versuchsvorschrift
1,8-Naphthyridin-2-ol (2.80 g, 19.16 mmol) was suspended in phosphorus oxychloride (100 ml, 1092 mmol) and heated at gentle reflux. The chlorination was followed by LC/MS and once the conversion was complete the reaction was evaporated to dryness and the residue partitioned between water (400 mL) and ethyl acetate (2×400 mL). The aqueous was extracted with additional ethyl acetate (2×400 mL). The combined organic layers were dried with magnesium sulfate and evaporated to dryness under reduced pressure. The crude compound was used without further purification.
Aufarbeitung
- temperatureheated at gentle reflux
- customwas evaporated to dryness
- customthe residue partitioned between water (400 mL) and ethyl acetate (2×400 mL)
- extractionThe aqueous was extracted with additional ethyl acetate (2×400 mL)
- dry with materialThe combined organic layers were dried with magnesium sulfate
- customevaporated to dryness under reduced pressure
- customThe crude compound was used without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-4298614be6074d24adcb8a43ac2001c0
- Quelldatensatz
- uspto-grants-2015_11
- Patentnummer
- US09174992B2
Verknüpfte Notizen
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