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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895273생성일: 2026년 10월 25일

Borane → 2'-o-Phthalimidoethyl-5-methyluridine

https://huagongshe.com/reaction/895273

반응식

참여 물질

역할이름HCID투입량
반응물BoraneHCID 6331—
반응물N-(2-Hydroxyethyl)phthalimideHCID 77499—
반응물2,2'-Anhydro-1-beta-arabinofuranosylthymineHCID 168045—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178418361HCID 178418361—
용매TetrahydrofuranHCID 8028—
용매Ethylacetate methanolHCID 21584119—
생성물2'-o-Phthalimidoethyl-5-methyluridineHCID 10002839—

반응 조건

온도150 °C

반응 단계

N-(2-Hydroxyethyl)phthalimide (277 g, 1.45 mol) was slowly added to a solution of borane in tetrahydrofuran (1 M, 600 mL), with stirring. Hydrogen gas evolved as the solid dissolved. Once the rate of gas evolution subsided, the solution was placed in a 2 L stainless steel bomb. 2,2′-Anhydro-5-methyluridine (60 g, 0.25 mol) and sodium bicarbonate (120 mg) were added and the bomb was sealed. After 30 minutes, the bomb was vented and placed in an oil bath and heated to 150° C. internal temperature for 24 h. The bomb was cooled to room temperature and opened. TLC (ethyl acetate-methanol; 95:5) revealed the disappearance of starting material. The crude solution was concentrated and the residue was purified by chromatography on silica gel starting with ethyl acetate to remove the excess phthalimide reagent, followed by ethyl acetate-methanol (95:5) to elute 2 (22.2 g, 20.6%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06914148B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-68def3d70d674509bda6cfce76cf84a2
출처 메모uspto-grants-2005_07