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HRID 539738作成日:2026年10月25日

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

https://huagongshe.com/reaction/539738

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物6-Methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 68089155—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒Sodium BicarbonateHCID 516892—
生成物3-Bromo-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazineHCID 6808904894%

反応条件

温度60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871767B2
出典データセットuspto-grants-2014_10
ORD IDord-344448864cad43119ae634d045403660
出典メモuspto-grants-2014_10