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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1360434Erstellt: 25. Oktober 2026

Sodium Iodide → 4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/1360434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktPhthalimide potassium saltHCID 24194345—
Edukt4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrileHCID 66958265—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrileHCID 6695841871,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Potassium phthalimide (954 mg, 5.15 mmol), sodium iodide (130 mg, 0.86 mmol), and DMF (5 mL) were added to 4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrile (1.0 g, 3.4 mmol, prepared as described in Parts A-E of Example 19), and the reaction was heated at 100° C. for 45 minutes under a nitrogen atmosphere and allowed to cool to ambient temperature. Water (50 mL) was added, and the resulting mixture was stirred at 0° C. A precipitate formed, was isolated by filtration, and was dissolved in chloroform. The resulting solution was dried over sodium sulfate, filtered, and concentrated under reduced pressure. An analysis by nuclear resonance spectroscopy (NMR) indicated that starting material was present. The solid was treated with potassium phthalimide (1.27 g, 6.88 mmol), sodium iodide (130 mg, 0.86 mmol), and DMF (5 mL) and heated at 90° C. for three hours. Water (50 mL) was added, and the resulting solid was isolated by filtration to provide 0.97 g of 4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrile as a gray, crystalline solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879849B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-9bfbb018d7e8437199b1c3c09ca184d7
Quellennotizuspto-grants-2011_02