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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539732생성일: 2026년 10월 25일

Acetic Acid → 5-(6-Methoxyimidazo[1,2-b]pyridazin-2-yl)-2-methylaniline

https://huagongshe.com/reaction/539732

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물6-Methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 68089155—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물5-(6-Methoxyimidazo[1,2-b]pyridazin-2-yl)-2-methylanilineHCID 5290382073.7%

반응 조건

온도80 °C

반응 단계

To a stirred solution of 6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine (0.5 g, 1.75 mmol) in ethanol (20 mL) and water (5 mL) containing AcOH (10.5 mmol) is added iron (0.491 g, 8.79 mmol). The mixture is heated at 80° C. for 4 hours, cooled, concentrated under reduced pressure, and sat. aqueous NaHCO3 (100 mL) is added. The mixture is extracted with EtOAc (3×50 mL), the organic layer is collected, dried over Na2SO4, filtered and concentrated to dryness. The crude product is purified via chromatography (hexanes to EtOAc) to afford the title compound (0.328 g, 73%) as a light yellow solid: Rf 0.21 (EtOAc); LCMS (m/z)=255.5 [M+H]+, tR=4.89 min. (10 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871767B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-ddd418ae27974b6d932f4c31091df64e
출처 메모uspto-grants-2014_10