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HRID 1358087作成日:2026年10月27日

Borane → 2'-o-Phthalimidoethyl-5-methyluridine

https://huagongshe.com/reaction/1358087

反応式

関与物質

役割名称HCID仕込み量
反応物BoraneHCID 6331—
反応物N-(2-Hydroxyethyl)phthalimideHCID 77499—
反応物2,2'-Anhydro-1-beta-arabinofuranosylthymineHCID 168045—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 178418361HCID 178418361—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethylacetate methanolHCID 21584119—
生成物2'-o-Phthalimidoethyl-5-methyluridineHCID 10002839—

反応条件

温度150 °C

反応手順

N-(2-Hydroxyethyl)phthalimide (277 g, 1.45 mol) was slowly added to a solution of borane in tetrahydrofuran (1 M, 600 mL), with stirring. Hydrogen gas evolved as the solid dissolved. Once the rate of gas evolution subsided, the solution was placed in a 2 L stainless steel bomb. 2,2′-Anhydro-5-methyluridine (60 g, 0.25 mol) and sodium bicarbonate (120 mg) were added and the bomb was sealed. After 30 minutes, the bomb was vented and placed in an oil bath and heated to 150° C. internal temperature for 24 h. The bomb was cooled to room temperature and opened. TLC (ethyl acetate-methanol; 95:5) revealed the disappearance of starting material. The crude solution was concentrated and the residue was purified by chromatography on silica gel starting with ethyl acetate to remove the excess phthalimide reagent, followed by ethyl acetate-methanol (95:5) to elute 2 (22.2 g, 20.6%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06593466B1
出典データセットuspto-grants-2003_07
ORD IDord-2314e7c75e404e09a27522b06028cd6b
出典メモuspto-grants-2003_07