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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835716Generated: October 26, 2026

Potassium Cyanide → (R)-1-(5-acetoxyhexyl)-7-benzyl-8-cyano-3-methylxanthine

https://huagongshe.com/reaction/1835716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactant(R)-1-(5-Acetoxyhexyl)-7-benzyl-8-bromo-3-methylxanthineHCID 54190334—
SolventDimethyl SulfoxideHCID 679—
Product(R)-1-(5-acetoxyhexyl)-7-benzyl-8-cyano-3-methylxanthineHCID 5381200890%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of (R)-1-(5-acetoxyhexyl)-7-benzyl-8-bromo-3-methylxanthine (9.55 g, 20.0 mmol) in anhydrous dimethylsulfoxide was added potassium cyanide (1.43 g, 22.0 mmol). After stirring at 70-80° C. for 4.5 hours, the mixture was cooled to room temperature, quenched with water (500 ml) and extracted with ethyl acetate (4×150 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (45 ml), dried over magnesium sulfate and the solvent was evaporated under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:1) to provide (R)-1-(5-acetoxyhexyl)-7-benzyl-8-cyano-3-methylxanthine (7.60 g, 90% yield) as a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774130B2
Source datasetuspto-grants-2004_08
ORD IDord-08972332c7154570be0419aa22ed38fb
Source noteuspto-grants-2004_08