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HRID 1031864作成日:2026年10月26日

5'-Amino-2',5'-dideoxy-5-ethyluridine → 2',5'-dideoxy-5-ethyl-5'-[2(RS)-(2,4-dichlorophenoxy)propylamino]uridine

https://huagongshe.com/reaction/1031864

反応式

関与物質

役割名称HCID仕込み量
反応物5'-Amino-2',5'-dideoxy-5-ethyluridineHCID 451828—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物2-(2,4-Dichlorophenoxy)propanalHCID 22166359—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物2',5'-dideoxy-5-ethyl-5'-[2(RS)-(2,4-dichlorophenoxy)propylamino]uridineHCID 1863617632.2%

反応手順

To a solution, cooled in ice, of 0.45 g of 5'-amino-2',5'-dideoxy-5-ethyluridine in 28 ml of methanol and 9 ml of water were added 0.17 g of sodium cyanoborohydride followed by 0.5 g of 2-(2,4-dichlorophenoxy)propionaldehyde. The mixture was allowed to warm to room temperature and was then stirred at room temperature for 3 days. The solution was concentrated in order to remove methanol, diluted with 20 ml of water and extracted three times with 15 ml of methylene chloride. The combined extracts were dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using methanol/methylene chloride (1:12) for the elution. There was obtained 0.26 g of 2',5'-dideoxy-5-ethyl-5'-[2(RS)-(2,4-dichlorophenoxy)-propylamino]uridine, mp 51°-61° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04956346
出典データセットuspto-grants-1990_09
ORD IDord-e642e6b0bb014088b8fa478578be2c08
出典メモuspto-grants-1990_09