참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Paraxanthine | HCID 4687 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (R)-5-Acetoxy-1-bromohexane | HCID 12619445 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | (R)-5-Acetoxy-1-bromohexane | HCID 12619445 | — |
| 생성물 | (R)-3-(5-acetoxyhexyl)-1,7-dimethylxanthine | HCID 54338253 | 120.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06878715B1 |
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| 출처 데이터셋 | uspto-grants-2005_04 |
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| ORD ID | ord-eea38e1cd00243098f2f44ca1f1f7377 |
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| 출처 메모 | uspto-grants-2005_04 |
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