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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413105생성일: 2026년 10월 24일

Ethanol → (2s,3r,5s)-5-(6-Amino-9h-Purin-9-Yl)-Tetrahydro-2-(Hydroxymethyl)furan-3-Ol

https://huagongshe.com/ko/reaction/413105

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물DeoxyadenosineHCID 13730—
용매WaterHCID 962—
생성물(2s,3r,5s)-5-(6-Amino-9h-Purin-9-Yl)-Tetrahydro-2-(Hydroxymethyl)furan-3-OlHCID 489519—

반응 단계

mp 189-190° C. (EtOH 95) (identical to commercial 2′-deoxy-D-adenosine) 1H NMR (200 MHz, DMSO-D6):δ 8.35 and 8.14 (2s, 2H, H2 and H8), 7.34 (s1, 2H, NH2), 6.35 (dd, 1H, H1′, J 6.1 Hz, J 7.85 Hz), 5.33 (d, 1H, OH2′, J 4.0 Hz), 5.28 (dd, 1H, H3′, J 4.95 Hz; J 6.6 Hz), 4.42 (m, 1H, OH5′), 3.88 (m, 1H, H4′), 3.63-3.52 (m, 2H, H5′a and H5′b), 2,71 (m, 1H, H2′a), 2.28 (m, 1H, H2′b). (identical to commercial 2′-deoxy-D-adenosine) αD+26° (c 0.5 water) (commercial 2′-deoxy-D-adenosine −25° (c 0.5 water)). UV λmax 260 nm (ε 14100) (H2O). Mass analysis (FAB+, GT) m/z 252 (M+H)+, 136 (BH2)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06566344B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-f16098e320f245378f5d7ed5e384e0d7
출처 메모uspto-grants-2003_05