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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37069생성일: 2026년 10월 23일

Adenine → 2'-Fluoro-2'-deoxyadenosine

https://huagongshe.com/ko/reaction/37069

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참여 물질

역할이름HCID투입량
반응물AdenineHCID 190—
반응물ThymidineHCID 5789—
반응물2'Fluoro-2'-deoxyuridineHCID 150851—
반응물Potassium azideHCID 10290740—
용매Potassium Phosphate, TribasicHCID 62657—
생성물2'-Fluoro-2'-deoxyadenosineHCID 100253—

반응 조건

온도37 °C

반응 단계

Adenine (Mann Research Laboratories, Inc., 0.8 g, 5.9 mmoles) and 1-(2-deoxy-2-fluoro-β-D-ribofuranosyl)uracil (0.4 g; 1.6 mmoles) which may be prepared according to J. F. Codington et al. (J. Org. Chem. 29:558, 1964) were suspended in 20 ml of 10 mM potassium phosphate buffer, pH 7.0, which contained 0.04% (w/v) potassium azide. Thymidine phosphorylase (2,400 I.U.) and purine nucleoside phosphorylase (3,900 I.U.) (T. A. Krenitsky et al., Biochemistry 20:3615, 1981 and U.S. Pat. No. 4,381,344) were added and the suspension stirred at 37° C. On day 6, the reaction was diluted to 100 ml with 5 mM potassium phosphate buffer, pH 7.0, which contained 0.04% (w/v) potassium azide. On day 17, the suspension was filtered and the filtrate was evaporated. The residue was suspended in warm water. The suspension was filtered and the filtrate applied to a 1.5×12 cm column of anion exchange resin (Bio-Rad AG1X2-hydroxide form). The product was eluted with water. Product containing fractions were combined and the solvent removed under vacuum. The residue was dissolved in water and lyophilized to obtain the title compound that analyzed as a 0.6 hydrate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420115
출처 데이터셋uspto-grants-1995_05
ORD IDord-492f07f3c31d4e92a53dd1a1c1b0a219
출처 메모uspto-grants-1995_05