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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1663817Erstellt: 24. Oktober 2026

Dimethylformamide → N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-2-cyclopropylacetamide

https://huagongshe.com/de/reaction/1663817

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
Edukt3-AminophenolHCID 11568—
Edukt2-cyclopropyl-N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamideHCID 57441030—
LösungsmittelTetrahydrofuran ethyl acetateHCID 21939870—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktN-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-2-cyclopropylacetamideHCID 5750555233%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

A mixture of 2-cyclopropyl-N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamide (501 mg, 1.46 mmol), 3-aminophenol (479 mg, 4.39 mmol), potassium carbonate (807 mg, 5.84 mmol) and N,N-dimethylformamide (5 mL) was stirred at 120° C. for 12 hr. Tetrahydrofuran/ethyl acetate and saturated brine were added to the reaction mixture, and insoluble material was filtered off. The filtrate was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=20/80→0/100) to give the title compound (156 mg, 33%) as a pale-yellow powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08034812B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-a2c21adf87bd4b14a8dcb517988c9981
Quellennotizuspto-grants-2011_10