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HRID 1663633作成日:2026年10月24日

Thionyl Chloride → 2-cyclopropyl-N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamide

https://huagongshe.com/ja/reaction/1663633

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物Cyclopropaneacetic acidHCID 138440—
反応物Sodium BicarbonateHCID 516892—
反応物6-Iodoimidazo[1,2-B]pyridazin-2-amineHCID 57441024—
触媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
溶媒DimethylacetamideHCID 31374—
生成物2-cyclopropyl-N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamideHCID 5744103072%

反応手順

To a solution of cyclopropylacetic acid (441 mg, 4.4 mmol) in tetrahydrofuran (8.0 mL) were added N,N-dimethylformamide (1 drop) and thionyl chloride (0.32 mL, 4.4 mmol), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated under reduced pressure, and dissolved in N,N-dimethylacetamide (2.0 mL). To a solution of 6-iodoimidazo[1,2-b]pyridazin-2-amine (1.04 g, 4.0 mmol) in N,N-dimethylacetamide (6.0 mL) was added dropwise the above-mentioned solution under ice-cooling. The mixture was stirred at room temperature for 2 hr. Under ice-cooling, aqueous sodium hydrogencarbonate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by basic silica gel column chromatography (ethyl acetate/hexane=80/20→100/0), and recrystallized from ethyl acetate to give the title compound (982 mg, 72%) as pale-green crystals.

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-4daf63df2b4945d1a15612baa9bdf85e
出典メモuspto-grants-2011_10