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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12886Erstellt: 25. Oktober 2026

2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → ethyl 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/12886

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
EduktCyclopentylhydrazine hydrochlorideHCID 212349—
EduktSodium AcetateHCID 517045—
LösungsmittelEthanolHCID 702—
Produktethyl 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylateHCID 1250812679,3%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Cyclopentyl-hydrazine hydrochloride (1.000 g; 7.32 mmol), ethyl (ethoxymethylene)-cyanoacetate (1.026 g, 6.61 mmol) and anhydrous sodium acetate (0.644 g, 7.85 mmol) were combined in ethanol (10 mL) and heated at 70° C. for 20 hours. After cooling to room temperature, ethanol was removed in vacuo and the residue was partitioned between methylene chloride and water. The organic phase was washed sequentially with water and brine. Each aqueous phase was back extracted with a single portion of methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated. Purification by flash chromatography, eluting with 10-40% EtOAc/hexanes yielded 5-amino-1-cyclopentyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.170 g, 73%). Mass spectrum: m/z: 224.1 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728029B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-660058880d6144ccbdfae5625f97875b
Quellennotizuspto-grants-2010_06