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HRID 1814941作成日:2026年10月26日

Sodium hydride → HCID 54432354、化合物

https://huagongshe.com/reaction/1814941

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物8-Bromo-3,7-dimethyl-3,7-dihydro-1H-purine-2,6-dioneHCID 702242—
反応物(R)-5-acetoxyhexyl-1-chlorohexaneHCID 86584512—
溶媒Dimethyl SulfoxideHCID 679—
生成物HCID 54432354HCID 5443235474%

反応手順

To a stirring suspension of sodium hydride (740 mg, 30.8 mmol) in anhydrous dimethylsulfoxide (120 ml) was added 8-bromo-3,7-dimethylxanthine (6.5 g, 25.0 mmol). After stirring at room temperature under argon for 1.5 hours, (R)-5-acetoxyhexyl-1-chlorohexane (4.91 g, 27.5 mmol) was added and the mixture was stirred at 80° C. for 18 hours. After cooling to room temperature, the reaction mixture was quenched by addition of saturated aqueous sodium chloride solution (300 ml) and extracted with ethyl acetate (3x 50 ml). The combined extracts were washed with water (2x 20 ml), with saturated aqueous sodium chloride solution (20 ml) and dried over magnesium sulfate. After evaporation of the solvent under reduced pressure, the crude product was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1 :1) to provide (R)-1-(5-acetoxyhexyl)-8-bromo-3, 7-dimethylxanthine (7.38 g, 74% yield) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06878715B1
出典データセットuspto-grants-2005_04
ORD IDord-710423a91b5f4e68b7657277a6f60fdb
出典メモuspto-grants-2005_04