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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476842Generated: October 25, 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/476842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Amino-2',5'-dideoxy-5-ethyluridineHCID 451828—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(2,4-Dichlorophenoxy)propanalHCID 22166359—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2',5'-dideoxy-5-ethyl-5'-[2(RS)-(2,4-dichlorophenoxy)propylamino]uridineHCID 1863617632.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886785
Source datasetuspto-grants-1989_12
ORD IDord-f60a1a0662d849d0a79821f3e189e387
Source noteuspto-grants-1989_12