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HRID 1663817作成日:2026年10月26日

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

https://huagongshe.com/reaction/1663817

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物3-AminophenolHCID 11568—
反応物2-cyclopropyl-N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamideHCID 57441030—
溶媒Tetrahydrofuran ethyl acetateHCID 21939870—
溶媒Sodium chloride; waterHCID 57417360—
生成物N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-2-cyclopropylacetamideHCID 5750555233%

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08034812B2
出典データセットuspto-grants-2011_10
ORD IDord-a2c21adf87bd4b14a8dcb517988c9981
出典メモuspto-grants-2011_10