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HRID 1934826作成日:2026年10月25日

2-Nitroimidazole → 2-[2-Hydroxy-2-(2-nitro-1H-imidazol-1-yl)ethyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1934826

反応式

関与物質

役割名称HCID仕込み量
反応物2-NitroimidazoleHCID 10701—
反応物Potassium CarbonateHCID 11430—
反応物N-(2,3-Epoxypropyl)phthalimideHCID 21601—
溶媒EthanolHCID 702—
生成物2-[2-Hydroxy-2-(2-nitro-1H-imidazol-1-yl)ethyl]-1H-isoindole-1,3(2H)-dioneHCID 22338292—

反応手順

To a solution of N-(2,3-epoxypropyl)phthalimide (1) (Fluka, 25.0 g, 0.123 mol) in ethanol (200 mL), 2-nitroimidazole (2) (Nippon Ghosei, 14.5 g, 0.128 mol) and potassium carbonate (1.5 g) were added, and the reaction mixture was heated under reflux for 8 hrs. The reaction mixture was cooled and the yellow solid obtained was filtered and washed with ethanol (2×75 mL). The precipitate was transferred to a one liter beaker and water was added (500 mL). The mixture was stirred for 15 min. The yellow precipitate was filtered and the solid was washed with water (3×250 mL). 2-[2-hydroxy-2-(2-nitro-1H-imidazol-1-yl)ethyl]-1H-isoindole-1,3(2H)-dione (3) was obtained and dried under vacuum. Yield 32.8 g (85%). The product was pure by proton NMR and HPLC, and was used in the next step without further purification. A portion (˜2 g) of the solid was recrystallized from methanol. The melting point was 213-214° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06384232B1
出典データセットuspto-grants-2002_05
ORD IDord-985c93a083ba40549ef825e390880e58
出典メモuspto-grants-2002_05