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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490304생성일: 2026년 10월 23일

Uridine Diphosphate → rUrd.rUrd.P-P-P-P

https://huagongshe.com/ko/reaction/490304

반응식

참여 물질

역할이름HCID투입량
반응물Uridine DiphosphateHCID 6031—
반응물TributylamineHCID 7622—
반응물Ammonium BicarbonateHCID 14013—
반응물TributylammoniumHCID 3724478—
반응물Disodium uridine 5'-diphosphateHCID 11957711—
반응물Diuridine tetraphosphate tetrasodium saltHCID 131724809—
생성물rUrd.rUrd.P-P-P-PHCID 131723853—

반응 단계

The present invention provides the synthesis of diuridine tetraphosphate tetrasodium salt via the tetraammonium salt. In this process, uridine 5′-diphosphate disodium salt is first converted to the tributylammonium salt using a sulfonic acid resin to generate UDP as the free acid, followed by salt formation with excess tributylamine. After isolation by evaporative water removal, the anhydrous UDP tributylammonium salt is activated with 1,1-carbonyldiimidazole in DMF solution, during which time coupling to form U2P4 also occurs. Concentration of the solution in vacuo, followed by ion-exchange chromatography on Sephadex DEAE-A25 using an increasing gradient of aqueous ammonium bicarbonate yielded a solution of pure diuridine tetraphosphate in ammonium bicarbonate buffer. The volatile buffer is removed by repeated evaporation with water on a rotary evaporator to generate the tetraammonium salt of U2P4 as oil. The oil is dissolved in deionized water to give a ca. 10% solution, and this solution is charged to a Dowex 50W×4 Na+ (Dow) column and eluted with deionized water. The fractions containing U2P4 are pooled, concentrated and lyophilized to yield U2P4 tetrasodium salt as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528119B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-7cf56a01c44540d3a55d570d2b60c997
출처 메모uspto-grants-2009_05