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HRID 514630作成日:2026年10月25日

Potassium Carbonate → 1-(2,2-Dihydroxymethyl-3-fluoropropyl)-4-hydroxymethyl-2-nitroimidazole

https://huagongshe.com/reaction/514630

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物2,2,2-CryptandHCID 72801—
反応物Potassium FluorideHCID 522689—
反応物HCID 89472108HCID 89472108—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物1-(2,2-Dihydroxymethyl-3-fluoropropyl)-4-hydroxymethyl-2-nitroimidazoleHCID 89472347—

反応条件

温度80 °C

反応手順

3.6 mg (7.6 μmol equivalents) of 2,2-dimethyl-5-[(4-methoxymethoxymethyl-2-nitro-1H-imidazol-1-yl)methyl]-5-(p-toluenesulfonyloxymethyl)-1,3-dioxane was dissolved in 1 mL of acetonitrile, 17 mg (34.5 μmol equivalents) of Kryptofix 222 (trade name, Merck), 5.8 mg (100 μmol equivalents) of potassium fluoride, and 1.8 mg (23 μmol equivalents) of potassium carbonate were added thereto, and the mixture was refluxed while heating for 3 hours. After completion of the reaction, water was added, and the mixture was extracted three times with chloroform. The combined chloroform layers were dried with anhydrous sodium sulfate and then concentrated under vacuum. The obtained crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (v/v)=1/1). 1 mL of 1 mol/L hydrochloric acid was added dropwise to a fraction thus obtained, and the mixture was heated to 80° C. in an oil bath and then stirred for 50 minutes. After completion of the reaction, the mixture was concentrated under vacuum to give a trace amount of 1-(2,2-dihydroxymethyl-3-fluoropropyl)-4-hydroxymethyl-2-nitroimidazole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09107964B2
出典データセットuspto-grants-2015_08
ORD IDord-32b6acceff8d494bbe86c5a677f48a98
出典メモuspto-grants-2015_08