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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2268372생성일: 2026년 10월 25일

Diisopropylethylamine → 2-[({9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}methyl)amino]-N,N-diisopropylacetamide

https://huagongshe.com/reaction/2268372

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-amino-N,N-bis(propan-2-yl)acetamideHCID 18348428—
반응물{9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}methyl methanesulfonateHCID 59975278—
생성물2-[({9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}methyl)amino]-N,N-diisopropylacetamideHCID 5997531111.3%

반응 단계

The title compound was prepared by a similar method to example 40 using {9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(methoxymethyl)tetrahydro-2-furanyl]-6-[(2,2-diphenylethyl)amino]-9H-purin-2-yl}methyl methanesulfonate (preparation 25) (374 mg, 0.66 mmol), 2-amino-N,N-diisopropylacetamide (520 mg, 3.3 mmol) (preparation 22) and N-ethyl-N-isopropyl-2-propanamine (170 mg, 1.32 mmol). The compound was purified by column chromatography on silica gel eluting with a solvent gradient of dichloromethane:methanol:ammonia (95:5:0.5) increasing in polarity to (90:10:1). The solvent was removed under reduced pressure to give a residue which was triturated with diethyl ether to give the title compound (47 mg) as a solid. MS: 632 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06326359B1
출처 데이터셋uspto-grants-2001_12
ORD IDord-a7654215ce2e4a19ae651f0bb3ffc60b
출처 메모uspto-grants-2001_12