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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1736052생성일: 2026년 10월 25일

Uridine → 9-beta-D-arabinofuranosyl-2-amino-6-iodo-9H-purine

https://huagongshe.com/reaction/1736052

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참여 물질

역할이름HCID투입량
반응물UridineHCID 6029—
반응물Uracil ArabinosideHCID 18323—
반응물2-Amino-6-iodopurineHCID 6101575—
반응물Potassium azideHCID 10290740—
용매Potassium Phosphate, TribasicHCID 62657—
생성물9-beta-D-arabinofuranosyl-2-amino-6-iodo-9H-purineHCID 5380200611%

반응 조건

온도37 °C

반응 단계

2-Amino-6-iodopurine (Sigma Chemicals, St. Louis. Mo.) (25.5 mmoles, 6.75 g) and uracil arabinoside (61.9 mmoles. 15.1 g) were combined in 0.31 liters of 10 mM potassium phosphate pH 6.9 with 0.02% potassium azide. Purified purine nucleoside phosphorylase (17000 units) and uridine phosphorylase (2000 units) were added and the solution stirred at 37° C. After 18 days an additional 5700 units of uridine phosphorylase were added. Fifty-seven days later the reaction was filtered and the flitrate chromatographed on a column containing XAD-2 resin (8×11 cm). The product was eluted with a step gradient of ethanol/water (v/v) as follows: 0.35 liter 10%; 1 liter 20%; 1 liter 50%; 0.2 liter 95%. Product-containing fractions were combined and the ethanol removed under vacuum. The residue was dissolved in 30% n-propanol/water (v/v) and chromatographed on a 7.5×90 cm column containing BioRad P-2 resin, This procedure yielded 1.1 g of 9-β-D-arabinofuranosyl-2-amino-6-iodo-9 H-purine as a 0.5 hydrate. NMR and mass spectrometry were consistent with the structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05539098
출처 데이터셋uspto-grants-1996_07
ORD IDord-1a1e16ea95be46ec8a9d3c0d42803855
출처 메모uspto-grants-1996_07