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HRID 985637作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/985637

反応式

関与物質

役割名称HCID仕込み量
反応物Uridine DiphosphateHCID 6031—
反応物TributylamineHCID 7622—
反応物Ammonium BicarbonateHCID 14013—
反応物TributylammoniumHCID 3724478—
反応物Disodium uridine 5'-diphosphateHCID 11957711—
反応物Diuridine tetraphosphate tetrasodium saltHCID 131724809—
生成物rUrd.rUrd.P-P-P-PHCID 131723853—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06872710B2
出典データセットuspto-grants-2005_03
ORD IDord-7c3ae6450c7a42018e55542fd2ea202a
出典メモuspto-grants-2005_03