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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1694674생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1694674

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물N-(1-((2R,3R,4S,5R)-5-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-3,4-dihydroxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamideHCID 10929984—
반응물2-Cyanoethyl chloromethyl etherHCID 11665405—
용매1,2-DichloroethaneHCID 11—
생성물4-N-acetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)cytidineHCID 8663072235%

반응 단계

N4-Acetyl-5′-O-(4,4′-dimethoxytrityl)cytidine (588 mg, 1 mmol) was dissolved in 4 mL of 1,2-dichloroethane, and 452 mg of diisopropylethylamine (3.5 mmol) was added thereto, and then 365 mg of dibutylstannyl dichloride (1.2 mmol) was further added. 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-cyanoethyl ether (1.3 mmol) was added dropwise, and the solution was stirred for 60 minutes. After the reaction completed, the reaction solution was added into an aqueous saturated sodium bicarbonate solution, and was extracted 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 N4-acetyl-5′-O-(4,4′-dimethoxytrityl)-2′-O-(2-cyanoethoxymethyl) cytidine (219 mg, yield 35%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158775B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-43d9a27bf16a4ed081b46b9d34773886
출처 메모uspto-grants-2012_04