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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | N'-(oxan-4-yl)(tert-butoxy)carbohydrazide | HCID 45092245 | — |
| Edukt | 1-(2,6-Difluoropyridin-3-YL)propan-1-one | HCID 53413972 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-ethyl-6-fluoro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine | HCID 59810791 | 83,9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07432266B2 |
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| Quelldatensatz | uspto-grants-2008_10 |
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| ORD ID | ord-2ce04c67934041968403a7312ecb8594 |
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| Quellennotiz | uspto-grants-2008_10 |
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