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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1663848생성일: 2026년 10월 23일

Dimethylformamide → 3-tert-butyl-N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/ko/reaction/1663848

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물3-tert-butyl-1-methyl-1H-pyrazole-5-carboxylic acidHCID 720529—
반응물N-[6-(3-amino-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamideHCID 57505476—
용매TetrahydrofuranHCID 8028—
용매DimethylacetamideHCID 31374—
생성물3-tert-butyl-N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1-methyl-1H-pyrazole-5-carboxamideHCID 5750558641%

반응 단계

Using 3-tert-butyl-1-methyl-1H-pyrazole-5-carboxylic acid (61 mg, 0.33 mmol), tetrahydrofuran (1.8 mL), N,N-dimethylformamide (30 μL, 0.39 mmol), oxalyl chloride (44 μL, mmol), N-[6-(3-amino-4-methylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide (90 mg, 0.28 mmol) and N,N-dimethylacetamide (1.8 mL), and in the same manner as in Example 119, the title compound (55 mg, 41%) was obtained as a white powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08034812B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-bbabf7edbc454017b256c8381a9de83d
출처 메모uspto-grants-2011_10