Water → 7-Bromo-9-fluoro-1-methyl-4,5-dihydro-[1,2,4]triazolo[4,3-a]quinoline
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([F:12])[CH:11]=1)[NH:8][C:7](=S)[CH2:6][CH2:5]2.[C:14]([NH:17][NH2:18])(=O)[CH3:15].C(OCC)(=O)C.O>C(O)CCC>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([F:12])[CH:11]=1)[N:8]1[C:14]([CH3:15])=[N:17][N:18]=[C:7]1[CH2:6][CH2:5]2Komponenten
Versuchsvorschrift
A suspension of 6-bromo-8-fluoro-3,4-dihydroquinoline-2(1H)-thione (1-4, 1.71 g, 6.57 mmol) and acetohydrazide (0.58 g, 7.89 mmol) in n-butanol (7 mL) was refluxed for 18 h under inert atmosphere. After cooling down to ambient temperature, ethyl acetate (10 mL) and water (10 mL) were added. The organic phase was then separated and the water phase was extracted with ethyl acetate (5×10 mL). The combined organic phases were washed with brine and dried over Na2SO4; the combined organic layers were then evaporated under reduced pressure to yield the crude product. The crude compound was purified by flash chromatography on silica gel to obtain the title compound as a white solid; 1H NMR (DMSO-D6, 500 MHz) δ=7.79 (dd, J=2.0 Hz, JHF=11.0 Hz, 1H), 7.63 (s, 1H), 2.95 (br s, 4H), 2.46 (d, JHF=8.5 Hz, 3H).
Aufarbeitung
- temperaturewas refluxed for 18 h under inert atmosphere
- customThe organic phase was then separated
- extractionthe water phase was extracted with ethyl acetate (5×10 mL)
- washThe combined organic phases were washed with brine
- dry with materialdried over Na2SO4
- customthe combined organic layers were then evaporated under reduced pressure
- customto yield the crude product
- customThe crude compound was purified by flash chromatography on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-3576f3ab146a4661a64e6d4b9fc44f9f
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09278093B2
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