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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1250000생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1250000

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—
생성물2'-o-Phthalimidoethyl-5-methyluridineHCID 1000283990%

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 bubbling 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 for the last time and then placed in an oil bath and heated to 150° C. internal temperature for 24 hours. The bomb was cooled to room temperature and opened. TLC revealed all the starting material was gone. The crude solution was concentrated and the residue was columned on silica gel starting with straight ethyl acetate to remove the excess phthalimide reagent followed by ethyl acetate-methanol 95/5 to elute the product to give 22.2 g (20.6%) of ca 90% pure product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06335437B1
출처 데이터셋uspto-grants-2002_01
ORD IDord-d9c4b76605064fd0b929d8fdbe98ba41
출처 메모uspto-grants-2002_01