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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1506537Erstellt: 24. Oktober 2026

Diisopropylethylamine → ethyl 1-(5-fluoropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/de/reaction/1506537

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktEthyl ethoxymethylene-3-oxo-4,4,4-trifluorobutyrateHCID 6185754—
Edukt5-Fluoro-2-hydrazinylpyridine hydrofluorideHCID 71721388—
LösungsmittelEthanolHCID 702—
Produktethyl 1-(5-fluoropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 6717137329,7%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To (E)-ethyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoate (0.441 g, 1.835 mmol) in ethanol (2 mL) was added diisopropylethylamine (0.427 mL, 2.447 mmol) followed by 5-fluoro-2-hydrazinylpyridine, hydrofluoride (0.3 g, 2.039 mmol) dissolved in 1 mL of ethanol (slightly exothermic). The reaction mixture was heated at 80° C. for 1 h. The reaction mixture was concentrated under reduced pressure, dissolved in dichloromethane (2 mL) and subjected to column chromatography using an ISCO setup (40 g, RediSep® silica gel column). The desired fractions were collected and concentrated to yield ethyl 1-(5-fluoropyridin-2-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate (0.165 g, 27%) as a white solid. LC/MS M+1=304.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09216972B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-a4f8b5e232224f2db07a166844118c3d
Quellennotizuspto-grants-2015_12