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HRID 1814913作成日:2026年10月25日

Water → (R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine

https://huagongshe.com/reaction/1814913

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ParaxanthineHCID 4687—
反応物Sodium hydrideHCID 24758—
反応物(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
溶媒Dimethyl SulfoxideHCID 679—
生成物(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
生成物(R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthineHCID 54338253120.5%

反応条件

温度80 °C

反応手順

To a stirring solution of 1,7-dimethylxanthine (0.30 g, 1.67 mmol) in dimethylsulfoxide (20 ml) was added sodium hydride (42 mmg, 1.75 mmol) in one portion. After stirring for 30 minutes, (R)-5-acetoxy-1-bromohexane (0.31 g, 1.75 mmol) was added next. (R)-5-Acetoxy-1-bromohexane was prepared according to methods described in U.S. patent application Ser. No. 09/002,345, which is incorporated herein by reference. After heating at 80° C. for 18 hours, water (25 ml) was added and the aqueous solution was extracted with dichloromethane (3×20 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (50 ml), dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica eluting with ethyl acetate to give (R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine (0.34 g, 64%, 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-eea38e1cd00243098f2f44ca1f1f7377
出典メモuspto-grants-2005_04