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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1814913생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1814913

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ParaxanthineHCID 4687—
반응물Sodium hydrideHCID 24758—
반응물(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
용매Dimethyl SulfoxideHCID 679—
생성물(R)-5-Acetoxy-1-bromohexaneHCID 12619445—
생성물(R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthineHCID 54338253120.5%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06878715B1
출처 데이터셋uspto-grants-2005_04
ORD IDord-eea38e1cd00243098f2f44ca1f1f7377
출처 메모uspto-grants-2005_04