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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1682086생성일: 2026년 10월 27일

Adenosine → 2-Amino-9-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1H-purin-6(9H)-one

https://huagongshe.com/reaction/1682086

반응식

참여 물질

역할이름HCID투입량
반응물AdenosineHCID 60961—
반응물(2R,3R,4S,5R)-5-(2,6-diaminopurin-9-yl)-4-fluoro-2-(hydroxymethyl)oxolan-3-olHCID 460081—
용매WaterHCID 962—
생성물2-Amino-9-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1H-purin-6(9H)-oneHCID 135434940—

반응 단계

2,6-Diamino-9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-purine (0.1 g, 0.35 mmoles) prepared as in Example 1, was dissolved in 10 ml of water. Calf intestine adenosine deaminase (10 I.U., Boehringer Mannheim) was added and the solution incubated at 37° C. for one day. The solvent was removed under vacuum. The residue was dissolved in acetonitrile/water (85/15) and chromatographed on silica gel with acetonitrile/water (85/15) as the solvent. Product containing fractions were combined and the solvent removed under vacuum. The residue was dissolved in water and lyophilization yielded 0.14 g of the title compound that analysed as a 1.1 hydrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05175274
출처 데이터셋uspto-grants-1992_12
ORD IDord-6a40a82f62af4dc1b7d291e61a3686bd
출처 메모uspto-grants-1992_12