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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539736생성일: 2026년 10월 25일

Acetic Acid → 5-(3-Chloro-6-methoxyimidazo[1,2-b]pyridazin-2-yl)-2-methylaniline

https://huagongshe.com/reaction/539736

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3-Chloro-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 68089122—
촉매IronHCID 23925—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물5-(3-Chloro-6-methoxyimidazo[1,2-b]pyridazin-2-yl)-2-methylanilineHCID 5751626789%

반응 조건

온도80 °C

반응 단계

To a stirred solution of 3-chloro-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine (0.25 g, 0.784 mmol) in ethanol (50 mL) and water (10 mL) containing AcOH (4.70 mmol) is added iron (0.218 g, 3.92 mmol). The reaction mixture is heated at 80° C. for 2 hours, cooled, concentrated under reduced pressure and sat. aqueous NaHCO3 (100 mL) is added. The mixture is extracted with EtOAc (3×50 mL). 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 (0.201 g, 89%) as a yellow solid: Rf 0.32 (EtOAc); LCMS (m/z)=289.4, 291.2 [M+H]+, tR=2.21 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871767B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-ea0b4462ee78402a8a736f7b50068a21
출처 메모uspto-grants-2014_10