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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1031864Erstellt: 25. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5'-Amino-2',5'-dideoxy-5-ethyluridineHCID 451828—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt2-(2,4-Dichlorophenoxy)propanalHCID 22166359—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt2',5'-dideoxy-5-ethyl-5'-[2(RS)-(2,4-dichlorophenoxy)propylamino]uridineHCID 1863617632,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04956346
Quelldatensatzuspto-grants-1990_09
ORD IDord-e642e6b0bb014088b8fa478578be2c08
Quellennotizuspto-grants-1990_09