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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

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloropurine ribosideHCID 93003—
반응물2-(2,5-dihydro-1H-pyrrol-1-yl)ethan-1-amineHCID 12973656—
용매EthanolHCID 702—
생성물N-[2-(2,5-dihydro-1H-pyrrol-1-yl) ethyl]adenosine, monohydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05055569
출처 데이터셋uspto-grants-1991_10
ORD IDord-9bfaf0fae7e84279aa4cb65aa267073f
출처 메모uspto-grants-1991_10