Trifluoroacetic acid → 3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine

HRID 2113718

Reaktionsgleichung

Reaktionsgleichung von HRID 2113718
[O:1]1[CH2:6][CH2:5][CH:4]([NH:7][NH:8]C(OC(C)(C)C)=O)[CH2:3][CH2:2]1.FC(F)(F)C(O)=O.F[C:24]1[C:29]([C:30](=O)[CH2:31][CH3:32])=[CH:28][CH:27]=[C:26]([F:34])[N:25]=1>ClCCl>[CH2:31]([C:30]1[C:29]2[C:24](=[N:25][C:26]([F:34])=[CH:27][CH:28]=2)[N:7]([CH:4]2[CH2:5][CH2:6][O:1][CH2:2][CH2:3]2)[N:8]=1)[CH3:32]

Komponenten

5

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

A mixture of tert-butyl 2-(tetrahydro-2H-pyran-4-yl)hydrazinecarboxylate (3.8 g, 0.018 mol) and trifluoroacetic acid (20 mL, 0.3 mol) were stirred in dichloromethane (20 mL) for 90 minutes. The mixture was concentrated, and the residue was taken up in acetonitrile (30 mL). 1-(2,6-difluoropyridin-3-yl)propan-1-one (2.34 g, 0.0137 mol) was then added, and the resulting mixture was stirred at 75° C. for 72 hours. After cooling to room temperature, the mixture was concentrated, and the residue was purified by flash chromatography on silica gel using a 10-50% hexane:ethyl acetate gradient (flow rate 20 mL/min). The organics were combined and the crude product was then extracted with ethyl acetate. The combined extracts were washed with saturated sodium bicarbonate and then concentrated to afford 2.86 g (83.9%) of 3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine as a white solid. LC/MS (EI) tR 3.5 (Method E), m/z 250 (M++1).

Aufarbeitung

  1. concentrationThe mixture was concentrated
  2. temperatureAfter cooling to room temperature
  3. concentrationthe mixture was concentrated
  4. customthe residue was purified by flash chromatography on silica gel using a 10-50% hexane
  5. extractionthe crude product was then extracted with ethyl acetate
  6. washThe combined extracts were washed with saturated sodium bicarbonate
  7. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-2ce04c67934041968403a7312ecb8594
Quelldatensatz
uspto-grants-2008_10
Patentnummer
US07432266B2

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