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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1663633생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물Cyclopropaneacetic acidHCID 138440—
반응물Sodium BicarbonateHCID 516892—
반응물6-Iodoimidazo[1,2-B]pyridazin-2-amineHCID 57441024—
촉매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매DimethylacetamideHCID 31374—
생성물2-cyclopropyl-N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamideHCID 5744103072%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08034812B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-4daf63df2b4945d1a15612baa9bdf85e
출처 메모uspto-grants-2011_10