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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10452생성일: 2026년 10월 24일

1,3-Propanediamine → N-(3-Aminopropyl)-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/ko/reaction/10452

반응식

참여 물질

역할이름HCID투입량
반응물1,3-PropanediamineHCID 428—
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-(3-Aminopropyl)-6-[(2,2-diphenylethyl)amino]-9-{(2R,3R,4S,5S)-5-[(ethylamino)carbonyl]-3,4-dihydroxytetrahydro-2-furanyl}-9H-purine-2-carboxamideHCID 6009169358.4%

반응 조건

온도100 °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) (0.35 g, 0.64 mmol) and 1,3-diaminopropane (0.45 g, 6.1 mmol) was heated at 100° C. for 3 hours. The mixture was dissolved in a little dichloromethane and purified by column chromatography on silica gel eluting with a gradient system of dichloromethane:methanol:concentrated aqueous ammonia (80:20:1.2, by volume) changing to dichloromethane methanol:concentrated aqueous ammonia (88:12:2, 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, (0.22 g, 58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094769B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f2ee14fab341482e9a74a7bb84f63a09
출처 메모uspto-grants-2006_08