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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814951Generated: November 1, 2026

Sodium hydride → HCID 23516881, compound

https://huagongshe.com/reaction/1814951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant6-AMINO-1-BENZYL-5-METHYLAMINOURACILHCID 726225—
Reactant5-(R)-Acetoxy-1-chlorohexaneHCID 11019434—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 23516881HCID 2351688147.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

6-Amino-1-benzyl-5-methylaminouracil (11 g, 43 mmol) was added to a suspension of sodium hydride (1.032 mg, 43 mmol) in anhydrous dimethylsulfoxide (75 ml). After stirring for 30 minutes, (R)-5-acetoxy-1-chlorohexane (7.675 g, 43 mmol) was added. The mixture was heated at 70-80° C. for 12 hours. After cooling to room temperature, the reaction was quenched by the addition of water (150 ml) and extracted with ethyl acetate (3x 125 ml). The combined extracts were washed with water (2x 50 ml), with saturated aqueous sodium chloride solution (50 ml), dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate to provide (R)-3-(5-acetoxyhexyl)-6-amino-1-benzyl-5-methylaminouracil (7.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878715B1
Source datasetuspto-grants-2005_04
ORD IDord-52ef98fa37b4440e90c7e525af8bf29a
Source noteuspto-grants-2005_04