Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345167생성일: 2026년 10월 25일
6-Chloropurine riboside → N-[2-(2,5-dihydro-1H-pyrrol-1-yl) ethyl]adenosine, monohydrochloride
https://huagongshe.com/reaction/345167
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 6-Chloropurine riboside | HCID 93003 | — |
| 반응물 | 2-(2,5-dihydro-1H-pyrrol-1-yl)ethan-1-amine | HCID 12973656 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | N-[2-(2,5-dihydro-1H-pyrrol-1-yl) ethyl]adenosine, monohydrochloride | HCID 131717027 | — |
반응 단계
To a suspension of 6 chloropurine riboside (1.27 g, 4.42 mmol) in 10 ml of absolute ethanol was added 2-(2,5-dihydro-1H-pyrrol-1-yl)-1-ethanamine (prepared in accordance with Arzneim. Forsch. 21 (12) 2089 (1971)) in an amount of 0.54 g (4.9 mmol). The reaction mixture was heated under reflux for 40 hours. Concentration of the reaction mixture in vacuo gave a residue which was chromatographed on cellulose powder (Whatman CC 31). The eluent was 85 parts n-butanol and 15 parts water. Fraction monitoring was accomplished by thin layer chromatography on silica gel (Kieselgel 60 F254) eluting with a mixture of 20 parts methanol, 79 parts methylene chloride and one part ammonium hydroxide. The chromatography gave a glass which was azeotroped with water 3 times to remove the n butanol. Lyophilization of the aqueous solution gave the title compound in an amount of 0.41 g (21g yield) as a white powder (mp 88°-105° C.)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05055569 |
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| 출처 데이터셋 | uspto-grants-1991_10 |
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| ORD ID | ord-9bfaf0fae7e84279aa4cb65aa267073f |
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| 출처 메모 | uspto-grants-1991_10 |
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