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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1736053생성일: 2026년 10월 25일

Uridine → 9-beta-D-arabinofuranosyl-6-pyrrolidino-9H-purine

https://huagongshe.com/reaction/1736053

반응식

참여 물질

역할이름HCID투입량
반응물UridineHCID 6029—
반응물Uracil ArabinosideHCID 18323—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물6-(pyrrolidin-1-yl)-9H-purineHCID 756690—
생성물9-beta-D-arabinofuranosyl-6-pyrrolidino-9H-purineHCID 5418848968.6%

반응 조건

온도35 °C

반응 단계

6-Pyrrolidinopurine (Sigma Chemical Co., St. Louis, Mo.) (2.6 mmoles), 0.5 g, and uracil arabinoside (5.29 mmoles, 1.29 g) were suspended in 100 ml of a 10 mM potassium phosphate 0.04% potassium azide solution with a pH of 7.4. Purified uridine phosphorylase (6000 I.U.) and purine nucleoside phosphorylase (8400 I.U.) (Krenitsky, T. A., et al. Biochemistry, 20, 3615 (1981) and U.S. Pat. No. 4,381,344) were added and the suspension stirred at 35° C. Twenty days later the reaction was filtered and the filtrate chromatographed on a column containing Dowex-I-hydroxide resin (2.5×8 cm). The product was eluted from the column with 90% methanol/water (v/v). Fractions containing product were combined and the solvent removed under vacuum. The residue was dissolved in 50 ml of 30% n-propanol and water (v/v) and chromatographed on a BioRad P-2 column (5×90 cm). The product was eluted with 30% n-propanol/water (v/v). Product-containing fractions were combined and the solvent was removed under vacuum yielding 0.573 g of 9-β-D-arabinofuranosyl-6-pyrrolidino-9 H-purine. 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-5b85efe368104d799d1c50f79e1f3e32
출처 메모uspto-grants-1996_07