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HRID 558591作成日:2026年10月25日

Hydrogen Bromide → 6-Bromo-8-methylimidazo(1,2-a)pyridine

https://huagongshe.com/reaction/558591

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物Ethane, 2-bromo-1,1-diethoxy-HCID 74852—
反応物2-Amino-5-bromo-3-methylpyridineHCID 137934—
反応物Sodium BicarbonateHCID 516892—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
生成物6-Bromo-8-methylimidazo(1,2-a)pyridineHCID 526064772%

反応条件

温度23 °C

反応手順

To a solution of commercially available 2-amino-5-bromo-3-picoline (21.48 g, 115 mmol) and bromoacetaldehyde diethyl acetal (90%, 39.6 mL, 230 mmol) in EtOH (110 mL) was added 48% aq. HBr (11 mL) and the mixture was refluxed for 11 h. Cooled to 23° C., diluted with EtOAc, poured into sat. NaHCO3-sol., separated phases, washed with the organic layer with brine, dried over Na2SO4. Removal of the solvent in vacuum (not over 40° C. bath temperature) left an orange liquid, which was directly coated on silica gel for chromatography. Silica gel column filtration with heptane/EtOAc 50:50->0:100 gave the title compound as a light brown solid (17.36 g, 72%). MS (ISP) 211.0 [(M+H)+], 231.1 [(M+2+H)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08063048B2
出典データセットuspto-grants-2011_11
ORD IDord-dcdfa935409f4f7a83952a8c7320d98e
出典メモuspto-grants-2011_11