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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547254생성일: 2026년 10월 26일

2-(6-{[(1R,2R)-2-(phenylmethoxy)cyclopentyl]amino}purin-9-yl)(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol → 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]-purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol

https://huagongshe.com/reaction/547254

반응식

참여 물질

역할이름HCID투입량
반응물2-(6-{[(1R,2R)-2-(phenylmethoxy)cyclopentyl]amino}purin-9-yl)(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diolHCID 67193234—
촉매Palladium hydroxideHCID 9942167—
용매EthanolHCID 702—
용매CyclohexaneHCID 8078—
생성물2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]-purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diolHCID 67189486—

반응 단계

The 2-(6-{[(1R,2R)-2-(phenylmethoxy)cyclopentyl]amino}purin-9-yl)(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol obtained in Example 11 (22 g) was dissolved in ethanol (450 mL) and cyclohexane (200 mL). To this solution was added palladium hydroxide (20 mole %, 1 gram added initially, 1 gram after 6 hours, and 1 gram after 14 hours), and the reaction mixture was refluxed for 18 hours. The reaction mixture was filtered thru celite while still hot, and solvent removed from the filtrate under reduced pressure. The product was triturated with ethanol (20 mL), filtered, and washed with ethanol, to afford 2-{6-[((1R,2R)-2-hydroxycyclopentyl)amino]purin-9-yl}(4S,5S,3R)-5-(chloromethyl)oxolane-3,4-diol as a white powder).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939509B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-b50a3d9def8b4ebf91809c21f83afba4
출처 메모uspto-grants-2011_05