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HRID 466092作成日:2026年10月26日

Triethylamine → 3'-O-benzyl-2'-deoxy-3-(2-tetrahydrofuranyl)-5-fluorouridine

https://huagongshe.com/reaction/466092

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Tetrahydro-2-furyl acetateHCID 102657—
反応物Uridine, 2'-deoxy-5-fluoro-3'-O-(phenylmethyl)-HCID 10664574—
溶媒DichloromethaneHCID 6344—
生成物3'-O-benzyl-2'-deoxy-3-(2-tetrahydrofuranyl)-5-fluorouridineHCID 1371509177%

反応手順

A 1.32 g quantity of N,O-bis(trimethylsiliyl)-acetamide was added with stirring to a suspension of 0.40 g of 3'-O-benzyl-2'-deoxy-5-fluorouridine in 8 ml of dry dichloromethane at room temperature. To the mixture were added, after 4 hours, 0.32 g of 2-acetoxytetrahydrofuran and a solution of 0.1 ml of stannic chloride in 1.6 ml of dry dichloromethane. The mixture was stirred for 1.5 hours and neutralized with 0.64 ml of triethylamine and washed with water. The dichloromethane layer was concentrated and the residue was dissolved in 16 ml of methanol. To the solution was added 0.24 ml of acetic acid and the mixture was left to stand for 3 hours at 40° C. The solvent was distilled off and the residue was subjected to silica gel column chromatography to conduct a gradient elution using chloroform and mixtures of methanol (up to 4%) and chloroform, giving 0.3 g of the title compound in a yield of 77%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155113
出典データセットuspto-grants-1992_10
ORD IDord-de69e7d23ed543889cc9bb5412f07d5b
出典メモuspto-grants-1992_10