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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1663794생성일: 2026년 10월 25일

Dimethylformamide → N-[6-(3-amino-4-ethylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1663794

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참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물3-Amino-4-ethylphenolHCID 18320513—
반응물N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)cyclopropanecarboxamideHCID 57386058—
용매WaterHCID 962—
생성물N-[6-(3-amino-4-ethylphenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamideHCID 5750553470%

반응 조건

온도150 °C

반응 단계

A mixture of N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)cyclopropanecarboxamide (984 mg, 3.0 mmol), 3-amino-4-ethylphenol (617 mg, 4.5 mmol), potassium carbonate (829 mg, 6.0 mmol) and N,N-dimethylformamide (9 mL) was stirred at 150° C. for 24 hr. The reaction mixture was diluted with water and extracted with a mixed solvent of ethyl acetate/tetrahydrofuran (3:1). The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=50/50→0/100) and recrystallized from a mixed solvent of ethyl acetate/diisopropyl ether to give the title compound (706 mg, yield 70%) as a khaki solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08034812B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-e61cd628919c4e2a8830b16e7330ecf5
출처 메모uspto-grants-2011_10