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HRID 1376718作成日:2026年10月27日

5-Fluorouridine → Floxuridine

https://huagongshe.com/reaction/1376718

反応式

関与物質

役割名称HCID仕込み量
反応物5-FluorouridineHCID 9427—
反応物1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物FloxuridineHCID 5790—

反応手順

5.244 gms. (20 mMoles) of 5-fluorouridine is dissolved in 20 mL anhydrous pyridine and then dried under vacuum. This procedure is repeated at least one more time in order to make 5-fluorouridine devoid of moisture. The dried 5-fluorouridine is then dissolved in 20 mL of pyridine. 8.131 gms (24 mMoles, 1.2 eq.) of 4,4'-dimethoxy trityl chloride is added as solid in 4 fractions over a period of 2 hours. The reaction mixture is then stirred at room temperature overnight and is then diluted with 25 mL of dichloromethane and washed with saturated sodium bicarbonate solution. The aqueous layer is then washed with 20 mL dichloromethane. The organic layers are mixed and washed with saturated bicarbonate solution two more times. The organic layer is then dried over anhydrous sodium sulphate. The solvent is removed under vacuum to yield a yellow foam which is purified on a silica gel column using 90:10 chloroform:methanol as eluent. The 4, 4'-dimethoxytrityl derivative of 5-fluorodeoxyuridine is prepared in an analogous manner.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05663321
出典データセットuspto-grants-1997_09
ORD IDord-68889fa343d04731b1ecba2e33cd69d9
出典メモuspto-grants-1997_09