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HRID 2363677作成日:2026年10月25日

Diisopropylethylamine → N2-phenoxyacetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)guanosine

https://huagongshe.com/reaction/2363677

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Chloromethyl 2-cyanoethyletherHCID 86616731—
反応物N2-Phenoxyacetyl-5'-O-(4,4'-dimethoxytrityl)guanosineHCID 136368406—
溶媒1,2-DichloroethaneHCID 11—
生成物N2-phenoxyacetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)guanosineHCID 13636840548%

反応手順

N2-Phenoxyacetyl-5′-O-(4,4′-dimethoxytrityl)guanosine (720 mg, 1 mmol) was dissolved in 4 mL of 1,2-dichloroethane, and 452 mg of diisopropylethylamine (3.5 mmol) was added, and 365 mg of dibutylstannyl dichloride (1.2 mmol) was added subsequently. Then, the reaction was performed at room temperature for 1 hour. Then, the reaction was performed at 80° C., and 155.4 mg of chloromethyl 2-cyanoethylether (1.3 mmol) was added dropwise, and the solution was stirred for 60 minutes. After the reaction completed, the reaction solution was mixed with 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 30 g of silica gel column chromatography to obtain N2-phenoxyacetyl-5′-O-(4,4′-dimethoxytrityl)-2′-O-(2-cyanoethoxymethyl)guanosine (384 mg; yield 48%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08691970B2
出典データセットuspto-grants-2014_04
ORD IDord-5201b07a902943ab8bceec0ecda5614a
出典メモuspto-grants-2014_04