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HRID 1663916생성일: 2026년 10월 25일

Tetrahydrofuran → N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1-ethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1663916

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Oxalyl chlorideHCID 65578—
반응물1-Ethyl-1H-pyrazole-5-carboxylic acidHCID 565702—
반응물N-[6-(3-amino-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamideHCID 57505476—
촉매DimethylformamideHCID 6228—
용매DimethylacetamideHCID 31374—
생성물N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1-ethyl-1H-pyrazole-5-carboxamideHCID 5750565276%

반응 단계

In the same manner as in Example 259 and using 1-ethyl-1H-pyrazole-5-carboxylic acid (110 mg, 0.80 mmol), tetrahydrofuran (5 mL), N,N-dimethylformamide (1 drop), oxalyl chloride (83 μL, 0.97 mmol), N-[6-(3-amino-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide (200 mg, 0.62 mmol) and N,N-dimethylacetamide (7 mL) as starting materials, the title compound (210 mg, 75%) was obtained as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08034812B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-4989ad8972dc442489d5fd3fbebf5d23
출처 메모uspto-grants-2011_10