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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1694673생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1694673

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
반응물2'-O-(2-Cyanoethoxymethyl)uridineHCID 67278941—
용매MethanolHCID 887—
생성물5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)uridineHCID 6727929698%

반응 단계

2′-O-(2-Cyanoethoxymethyl)uridine (14 g, 43 mmol) was subjected to azeotropic distillation with pyridine, and then was dried with a vacuum pump for 30 minutes. The residue was dissolved in 300 mL of THF, and 68 g of pyridine (856 mmol), and 20 g of molecular sieve 4 A was added under an argon atmosphere, and the mixture was stirred for 10 minutes. To the solution was added 19.6 g of 4,4′-dimethoxytritylchloride (57.8 mmol) by 3 portions every 1 hour, and the mixture was further stirred for 1 hour. After 10 mL of methanol was added and the reaction solution was stirred for 2 minutes, the reaction solution was filtrated with a celite, and was washed with ethyl acetate. After concentrating the filtrate, the residue was dissolved in ethyl acetate, and was washed with a saturated aqueous sodium bicarbonate solution. After the organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, the solvent was distilled off. The obtained residue was purified by silica gel chromatography to obtain the objective compound (26.5 g, yield 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158775B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-8b15a528422e42f18dc837496157d8f1
출처 메모uspto-grants-2012_04