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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10442생성일: 2026년 10월 26일

Ethylenediamine → N-(2-aminoethyl)-6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxamide

https://huagongshe.com/reaction/10442

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참여 물질

역할이름HCID투입량
반응물EthylenediamineHCID 3301—
반응물Methyl 6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylateHCID 10187396—
용매DichloromethaneHCID 6344—
생성물N-(2-aminoethyl)-6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxamideHCID 1119242486.1%

반응 조건

온도105 °C

반응 단계

A mixture of methyl 6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxylate (Preparation 9) (1.1 g, 2 mmol) and 1,2-ethylenediamine (1.1 g, 18.3 mmol) was heated at 105° C. for 2.5 hours. The mixture was dissolved in a little dichloromethane and purified by column chromatography on silica gel eluting with dichloromethane:methanol:concentrated aqueous ammonia (85:15:1.5, by volume). After evaporation of appropriate fractions the residue was triturated with diethyl ether, filtered and dried to yield the target compound as a white solid, (0.99 g, 86%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094769B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-69e9be3268244ec6a9f9871f2e034f0a
출처 메모uspto-grants-2006_08