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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2113718Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/2113718

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktN'-(oxan-4-yl)(tert-butoxy)carbohydrazideHCID 45092245—
Edukt1-(2,6-Difluoropyridin-3-YL)propan-1-oneHCID 53413972—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridineHCID 5981079183,9%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07432266B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-2ce04c67934041968403a7312ecb8594
Quellennotizuspto-grants-2008_10