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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943459생성일: 2026년 10월 27일

8-(6-amino-4-chloropyridin-2-ylamino)-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamide → HCID 178507676, 화합물

https://huagongshe.com/reaction/1943459

반응식

참여 물질

역할이름HCID투입량
반응물8-(6-amino-4-chloropyridin-2-ylamino)-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamideHCID 59624351—
반응물HCID 178511674HCID 178511674—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물HCID 178507676HCID 17850767644.2%

반응 조건

온도110 °C

반응 단계

A mixture of 8-(6-amino-4-chloropyridin-2-ylamino)-6-chloro-N-(3-fluoropyridin-4-yl)imidazo[1,2-b]pyridazine-3-carboxamide (42 mg, 0.073 mmol) and trans-cyclohexane-1,4-diamine (74.2 mg, 0.650 mmol) in NMP (0.4 mL) was heated at 110° C. overnight. The reaction mixture was then cooled to room temperature and purified by reversed-phase HPLC. The fractions containing the title compounds were lyophilized to dryness to afford 8-((6-amino-4-chloro-2-pyridinyl)amino)-6-((trans-4-aminocyclohexyl)amino)-N-(3-fluoro-4-pyridinyl)imidazo[1,2-b]pyridazine-3-carboxamide (16.5 mg, 25%). HPLC Rt=2.813 minutes (Chromolith SpeedROD 4.6×50 mm, 10-90% aqueous methanol containing 0.1% TFA, 4 min gradient, monitored at 220 nm), [M+H]=511.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08389527B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-394a6520f00d4ee2bb459b5a86b724e0
출처 메모uspto-grants-2013_03