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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943434생성일: 2026년 10월 27일

6-chloro-N-(2-chloropyridin-4-yl)-8-(cyclopropyl(4-methoxybenzyl)amino)imidazo[1,2-b]pyridazine-3-carboxamide → HCID 178490954, 화합물

https://huagongshe.com/reaction/1943434

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참여 물질

역할이름HCID투입량
반응물6-chloro-N-(2-chloropyridin-4-yl)-8-(cyclopropyl(4-methoxybenzyl)amino)imidazo[1,2-b]pyridazine-3-carboxamideHCID 59624874—
반응물HCID 178511674HCID 178511674—
용매WaterHCID 962—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물HCID 178490954HCID 17849095498%

반응 조건

온도120 °C

반응 단계

6-chloro-N-(2-chloropyridin-4-yl)-8-(cyclopropyl(4-methoxybenzyl)amino)imidazo[1,2-b]pyridazine-3-carboxamide (9 g, 18.6 mmol) was combined with trans-1,4-diaminocyclohexane (31.9 g, 279 mmol) in N-methyl-2-pyrrolidinone (50 mL) and heated at 80° C. for 16 hours and at 120° C. for 6 hrs. The reaction was cooled to room temperature, and water (200 mL) was added, and the solid collected via Buchner filtration. The crude product was purified with silica gel chromatography using a stepwise gradient of 10% methanol/chloroform to 25% methanol/chloroform/1% triethylamine to isolated foamy solid. The solid was suspended in water (400 mL) and collected with Buchner filtration (2×50 mL water wash) and dried for 16 hrs under reduced pressure to afford 6-((trans)-4-aminocyclohexylamino)-N-(2-chloropyridin-4-yl)-8-(cyclopropyl(4-methoxybenzyl)amino)imidazo[1,2-b]pyridazine-3-carboxamide (10.2 g, 18.18 mmol, 98% yield) as a off white solid. LC/MS (Phenomenex Luna 5 micron C18 4.6×30 mm, 0 to 100 B in 2 min with 1 min hold time, Flow rate=5 mL/min, detection at 254 nm, Solvent A: 10% methanol/90% water/0.1% TFA; Solvent B: 10% water/90% methanol/0.1% TFA) Rt=1.77 minutes. [M+H]=561.16.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08389527B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-116d2d75317e4f3e887cf504bdbaf803
출처 메모uspto-grants-2013_03