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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539738생성일: 2026년 10월 24일

N-bromobutanimide → 3-Bromo-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine

https://huagongshe.com/ko/reaction/539738

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물6-Methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 68089155—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Sodium BicarbonateHCID 516892—
생성물3-Bromo-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 6808904894%

반응 조건

온도60 °C

반응 단계

To a stirred solution of 6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine (0.250 g, 0.879 mmol) in acetonitrile (20 mL) is added N-bromosuccinimide (0.879 mmol) and the mixture is heated at 60° C. for 8 hours. The reaction mixture is diluted with water (50 mL) and sat. aqueous NaHCO3 (50 mL). The precipitate that forms is collected by filtration, washed with water (3×25 mL) and dried under vacuum to give the title product (0.300 g, 94% yield) as a yellow solid: Rf 0.51 (1:1 EtOAc:hexanes); LCMS (m/z)=363.2, 365.2 [M+H]+, tR=3.02 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871767B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-344448864cad43119ae634d045403660
출처 메모uspto-grants-2014_10