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HRID 1694677作成日:2026年10月25日

Diisopropylethylamine → 6-N-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)adenosine

https://huagongshe.com/reaction/1694677

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Sodium BicarbonateHCID 516892—
反応物2-Cyanoethyl chloromethyl etherHCID 11665405—
反応物Adenosine, N-acetyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-HCID 71356814—
溶媒1,2-DichloroethaneHCID 11—
生成物6-N-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)adenosineHCID 8663072433%

反応条件

温度80 °C

反応手順

N6-Acetyl-5′-O-(4,4′-dimethoxytrityl)adenosine (22.0 g, 36.0 mmol) was dissolved in 170 mL of 1,2-dichloroethane, and 16.3 g of diisopropylethylamine (126 mmol) was added, and 12.1 g of dibutylstannyl dichloride (39.7 mmol) was added subsequently. Then, the reaction was performed at room temperature for 1 hour. Then, the reaction solution was heated up to 80° C., and 4.30 g of chloromethyl 2-cyanoethyl ether (36.0 mmol) was added dropwise, and the solution was stirred for 30 minutes. After the reaction completed, the reaction solution was added to an aqueous saturated sodium bicarbonate solution, and was subjected to extraction with methylene chloride. The extract was dried over anhydrous magnesium sulfate, and the solvent was distilled off. The obtained mixture was purified by silica gel column chromatography to obtain N6-acetyl-5′-O-(4,4′-dimethoxytrityl)-2′-O-(2-cyanoethoxymethyl) adenosine (7.47 g, yield 33%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08158775B2
出典データセットuspto-grants-2012_04
ORD IDord-41417203306d4df692589c32184f1708
出典メモuspto-grants-2012_04