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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2391275생성일: 2026년 10월 26일

2,5-Dimethyl-2H-pyrazole-3-carbonyl chloride → N-[3-({2-[(N,N-dimethylglycyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/2391275

반응식

참여 물질

역할이름HCID투입량
반응물2,5-Dimethyl-2H-pyrazole-3-carbonyl chlorideHCID 2736299—
반응물N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-N2,N2-dimethylglycinamideHCID 57708553—
용매N-methyl-2-pyrrolidoneHCID 13387—
용매Sodium HydroxideHCID 14798—
생성물N-[3-({2-[(N,N-dimethylglycyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)phenyl]-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 2476798049%

반응 단계

To a solution of N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]-N2,N2-dimethylglycinamide (196 mg, 0.6 mmol) in N-methylpyrrolidone (5.0 mL) was added 1,3-dimethylpyrazole-5-carbonyl chloride (270 mg, 1.7 mmol), and the mixture was stirred at room temperature for 5 hr. The reaction mixture was diluted with 1N aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→460/40) and precipitated from ethyl acetate to give the title compound (131 mg, 49%) as a white powder. melting point 210° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08273741B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-bb0344d669744857a7803d339af9601e
출처 메모uspto-grants-2012_09