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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466105생성일: 2026년 10월 26일

Sodium Iodide → 2'-deoxy-5-fluoro-3'-O-(2,4,6-trimethylbenzyl)uridine

https://huagongshe.com/reaction/466105

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium HydroxideHCID 14797—
반응물2,4,6-Trimethylbenzyl chlorideHCID 74108—
반응물2'-deoxy-5'-O-trityl-5-fluorouridineHCID 10838704—
용매1,4-DioxaneHCID 31275—
생성물2'-deoxy-5-fluoro-3'-O-(2,4,6-trimethylbenzyl)uridineHCID 1407440855%

반응 조건

온도60 °C

반응 단계

A 1.66 g quantity of 2,4,6-trimethylbenzyl chloride was added to a solution of 4.00 g of 2'-deoxy-5-fluoro-5'-O-trityluridine, 2.30 g of potassium hydroxide and 1.47 g of sodium iodide in 50 ml of dried dioxane. The mixture was stirred at 60° C. for 3 hours. The solvent was distilled off, and ethylacetate and water were added to the residue. The ethyl acetate layer was washed with water and dried over anhydrous sodium sulfate. The ethyl acetate was distilled off and the residue was dissolved in 50 ml of a 80% solution of acetic acid. The resulting solution was left to stand at 70° C. for 2 hours. The reaction mixture was concentrated and water was added to the concentrate. The mixture was rendered weakly basic with an aqueous solution of sodium hydroxide and washed with ether. The aqueous layer was made weakly acidic with a 6N solution of hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous sodium sulfate and concentrated. Ether was added to the concentrate to deposit solids and the solids were recrystallized from ethanol, giving 1.69 g of the title compound in a yield of 55%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155113
출처 데이터셋uspto-grants-1992_10
ORD IDord-86fca4c3106b42fd8a7c7e95ed88cc2f
출처 메모uspto-grants-1992_10