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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1376718생성일: 2026년 10월 26일

5-Fluorouridine → Floxuridine

https://huagongshe.com/reaction/1376718

반응식

참여 물질

역할이름HCID투입량
반응물5-FluorouridineHCID 9427—
반응물1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물FloxuridineHCID 5790—

반응 단계

5.244 gms. (20 mMoles) of 5-fluorouridine is dissolved in 20 mL anhydrous pyridine and then dried under vacuum. This procedure is repeated at least one more time in order to make 5-fluorouridine devoid of moisture. The dried 5-fluorouridine is then dissolved in 20 mL of pyridine. 8.131 gms (24 mMoles, 1.2 eq.) of 4,4'-dimethoxy trityl chloride is added as solid in 4 fractions over a period of 2 hours. The reaction mixture is then stirred at room temperature overnight and is then diluted with 25 mL of dichloromethane and washed with saturated sodium bicarbonate solution. The aqueous layer is then washed with 20 mL dichloromethane. The organic layers are mixed and washed with saturated bicarbonate solution two more times. The organic layer is then dried over anhydrous sodium sulphate. The solvent is removed under vacuum to yield a yellow foam which is purified on a silica gel column using 90:10 chloroform:methanol as eluent. The 4, 4'-dimethoxytrityl derivative of 5-fluorodeoxyuridine is prepared in an analogous manner.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05663321
출처 데이터셋uspto-grants-1997_09
ORD IDord-68889fa343d04731b1ecba2e33cd69d9
출처 메모uspto-grants-1997_09