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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2393317생성일: 2026년 10월 24일

Thymidine → 5'-O-[(pyren-1-yl)methyl]thymidine

https://huagongshe.com/ko/reaction/2393317

반응식

참여 물질

역할이름HCID투입량
반응물ThymidineHCID 5789—
반응물DichloromethaneHCID 6344—
반응물Sodium hydrideHCID 24758—
반응물1-(Chloromethyl)pyreneHCID 97581—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
생성물5'-O-[(pyren-1-yl)methyl]thymidineHCID 228777926.4%

반응 단계

A mixture of 875 mg of sodium hydride (as a 55% w/w dispersion in mineral oil) in 5 ml of dimethyl sulfoxide was stirred at room temperature for 30 minutes in an atmosphere of nitrogen, and then a solution of 2.42 g (10 mmol) of thymidine in 5 ml of dimethyl sulfoxide was added dropwise to the resulting mixture. The mixture was stirred at room temperature for 30 minutes, after which a suspension of 2.51 g (10 mmol) of 1-(chloromethyl)pyrene [Acta Chem. Scand., 10, 1362 (1936)] in 15 ml of dimethyl sulfoxide was added. The mixture was then stirred at room temperature for 90 minutes. At the end of this time, the reaction mixture was poured into 100 ml of ice-water, and the aqueous mixture was extracted with 100 ml of ethyl acetate and then with 100 ml of methylene chloride. The extract was dried over anhydrous magnesium sulfate, and then the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through 150 g of silica gel (230-400 mesh), using a gradient elution method, with mixtures of methylene chloride containing from 0 to 4% by volume of methanol as the eluent, to give 292.4 mg (yield 6.4%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05807837
출처 데이터셋uspto-grants-1998_09
ORD IDord-e2cc5ea08e39489389e3825f458230e3
출처 메모uspto-grants-1998_09