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HRID 2372391作成日:2026年10月25日

Methane → 1-(2-Nitro-1-imidazolyl)-3-(2-fluoroethylamino)-2-propanol hydrochloride

https://huagongshe.com/reaction/2372391

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物Hydrochloric AcidHCID 313—
反応物2-NitroimidazoleHCID 10701—
反応物Sodium HydroxideHCID 14798—
反応物1-(2,3-Epoxypropyl)-2-nitroimidazoleHCID 334973—
反応物2-Fluoroethylazanium chlorideHCID 139190533—
溶媒EthanolHCID 702—
生成物1-(2-Nitro-1-imidazolyl)-3-(2-fluoroethylamino)-2-propanol hydrochlorideHCID 14621553—

反応手順

A mixture of 1-(2,3-epoxypropyl)-2-nitroimidazole prepared by the method described by Beaman et al. [Beaman, A.G., Tautz, W. and Duschinsky, R., 1968; Studies in the Nitroimidazole Series. III, Antimicrobial Agents and Chemotherapy, pp. 520-530] (4.00 g, 23.7 mmol), 2-fluoro-ethylammonium chloride (5.00 g, 50.2 mmol) and sodium hydroxide (2.00 g, 50.0 mmol) in ethanol (60 cm3) was stirred at 15° C. for 30 minutes then heated under reflux for 3 hours. The reaction mixture was then treated with decolourising charcoal (0.5 g), cooled and filtered. Concentration under reduced pressure afforded a pale yellow oil which was dissolved in ethanol (20 cm3) and treated with a small excess of anhydrous ethereal hydrogen chloride to give 1-(2-nitro-1-imidazolyl)-3-(2-fluoroethylamino)-2-propanol hydrochloride in the form of a pale yellow crystalline solid (4.38 g, 68.9%) after recrystallisation from aqueous ethanol, m.p. 178°-179° C. (dec. after drying in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05098921
出典データセットuspto-grants-1992_03
ORD IDord-7a5fb70cad7e4749b01cd15758d7333a
出典メモuspto-grants-1992_03