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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1694672생성일: 2026년 10월 26일

Diisopropylethylamine → 5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)uridine

https://huagongshe.com/reaction/1694672

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물2-Cyanoethyl chloromethyl etherHCID 11665405—
반응물5'-O-(Bis(4-methoxyphenyl)phenylmethyl)uridineHCID 11763309—
용매1,2-DichloroethaneHCID 11—
생성물5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)uridineHCID 6727929634%

반응 단계

5′-O-(4,4′-Dimethoxytrityl)uridine (546 mg, 1 mmol) was dissolved in 4 mL of 1,2-dichloroethane, and 452 mg of diisopropylethylamine (3.5 mmol) was added thereto, and 365 mg of dibutylstannyl dichloride (1.2 mmol) was further added thereto. The reaction was performed at room temperature for 1 hour. Subsequently, the reaction was performed at 80° C., and 155.4 mg of chloromethyl 2-cyanoethyl ether (1.3 mmol) was added dropwise, and the reaction solution was stirred for 30 minutes. After the reaction completed, the reaction solution was added into an aqueous saturated sodium bicarbonate solution, and was subjected to extraction with methylene chloride, and 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 5′-O-(4,4′-dimethoxytrityl)-2′-O-(2-cyanoethoxymethyl)uridine (197 mg, yield 34%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158775B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-35953b5aaac94f2fb0174fb4f50312d8
출처 메모uspto-grants-2012_04