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HRID 37069作成日:2026年10月24日

Adenine → 2'-Fluoro-2'-deoxyadenosine

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

反応式

関与物質

役割名称HCID仕込み量
反応物AdenineHCID 190—
反応物ThymidineHCID 5789—
反応物2'Fluoro-2'-deoxyuridineHCID 150851—
反応物Potassium azideHCID 10290740—
溶媒Potassium Phosphate, TribasicHCID 62657—
生成物2'-Fluoro-2'-deoxyadenosineHCID 100253—

反応条件

温度37 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420115
出典データセットuspto-grants-1995_05
ORD IDord-492f07f3c31d4e92a53dd1a1c1b0a219
出典メモuspto-grants-1995_05