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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490305생성일: 2026년 10월 23일

Uridine Monophosphate → rUrd.rUrd.P-P-P-P

https://huagongshe.com/ko/reaction/490305

반응식

참여 물질

역할이름HCID투입량
반응물Uridine MonophosphateHCID 6030—
반응물Uridine 5'-triphosphateHCID 6133—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물TributylammoniumHCID 3724478—
용매DimethylformamideHCID 6228—
용매TributylamineHCID 7622—
생성물rUrd.rUrd.P-P-P-PHCID 131723853—

반응 조건

온도50 °C

반응 단계

Uridine 5′-monophosphate (Sigma, Milwaukee, 3.0 g, 9.26 mmol) was dissolved in dry DMF (10 mL) and tributylamine (Aldrich, 2 mL). The solution was evaporated in vacuo at 40° C. to an oil. The residue was dissolved in dry DMF (Aldrich, 8 mL) to form a solution. Carbonyldiimidazole (Aldrich, 1.65 g, 10.18 mmol) was added to this solution. The reaction was heated at 50° C. for one hour. Uridine 5′-triphosphate (Yamasa, 5.60 g, 10.18 mmol) prepared as the anhydrous tributylammonium salt in DMF (5 mL) and tributylamine (2 mL), as described in Example 3 below, was added to the reaction solution. The mixture was allowed to stir at 50° C. for three days when the solution was evaporated in vacuo to an oil, redissolved in water (5 mL) and purified by column (300×50 mm) chromatography (Sephadex DEAE-A25, 40-120μ, Aldrich, pre-swollen in 1.0 M NaHCO3 and washed with 2 column volumes of deionized H2O (H2O→0.3 M NH4HCO3 gradient). The pure fractions were concentrated in vacuo at 35° C., and H2O added and reevaporated 5 times to obtain diuridine tetraphosphate tetrammonium salt as a white solid (2.37 g, 30% yield): 92.11% pure by HPLC with the same retention time as the standard. In addition, the tetrammonium salt was analyzed by FABMS to give a mass of [C18H25N4O23P4 (M-H+)−: calculated 788.9860] 788.9857, confirming a parent formula of C18H26N4O23P4 for the free acid].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528119B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-615cb5223874471b8fa987acac34d1d4
출처 메모uspto-grants-2009_05