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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2391245생성일: 2026년 10월 25일

Dimethylformamide → N-(3-{[2-(acetylamino)imidazo[1,2-b]pyridazin-6-yl]oxy}phenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/2391245

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물1,3-Dimethyl-1H-pyrazole-5-carboxylic acidHCID 587721—
반응물N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]acetamideHCID 57441053—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매DimethylacetamideHCID 31374—
생성물N-(3-{[2-(acetylamino)imidazo[1,2-b]pyridazin-6-yl]oxy}phenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5750550667%

반응 단계

To a solution (4.0 mL) of 1,3-dimethyl-1H-pyrazole-5-carboxylic acid (109 mg, 0.85 mmol) in tetrahydrofuran were added N,N-dimethylformamide (30 μL, 0.39 mmol) and oxalyl chloride (135 μL, 1.55 mmol), and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure, and a solution of the residue in N,N-dimethylacetamide (2.0 mL) was added dropwise to a solution of N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]acetamide (200 mg, 0.71 mmol) in N,N-dimethylacetamide (2.0 mL). After the reaction mixture was stirred at room temperature for 1 hr, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate/tetrahydrofuran, washed with saturated brine, dried over anhydrous magnesium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was washed with ethyl acetate to give the title compound (182 mg, 67%) as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273741B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-cd91b1807da24b31b86395eaff2c2c37
출처 메모uspto-grants-2012_09