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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466092생성일: 2026년 10월 25일

Triethylamine → 3'-O-benzyl-2'-deoxy-3-(2-tetrahydrofuranyl)-5-fluorouridine

https://huagongshe.com/reaction/466092

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tetrahydro-2-furyl acetateHCID 102657—
반응물Uridine, 2'-deoxy-5-fluoro-3'-O-(phenylmethyl)-HCID 10664574—
용매DichloromethaneHCID 6344—
생성물3'-O-benzyl-2'-deoxy-3-(2-tetrahydrofuranyl)-5-fluorouridineHCID 1371509177%

반응 단계

A 1.32 g quantity of N,O-bis(trimethylsiliyl)-acetamide was added with stirring to a suspension of 0.40 g of 3'-O-benzyl-2'-deoxy-5-fluorouridine in 8 ml of dry dichloromethane at room temperature. To the mixture were added, after 4 hours, 0.32 g of 2-acetoxytetrahydrofuran and a solution of 0.1 ml of stannic chloride in 1.6 ml of dry dichloromethane. The mixture was stirred for 1.5 hours and neutralized with 0.64 ml of triethylamine and washed with water. The dichloromethane layer was concentrated and the residue was dissolved in 16 ml of methanol. To the solution was added 0.24 ml of acetic acid and the mixture was left to stand for 3 hours at 40° C. The solvent was distilled off and the residue was subjected to silica gel column chromatography to conduct a gradient elution using chloroform and mixtures of methanol (up to 4%) and chloroform, giving 0.3 g of the title compound in a yield of 77%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155113
출처 데이터셋uspto-grants-1992_10
ORD IDord-de69e7d23ed543889cc9bb5412f07d5b
출처 메모uspto-grants-1992_10