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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355391Generated: November 2, 2026

Sodium Sulfide → HCID 178468220, compound

https://huagongshe.com/reaction/1355391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfideHCID 14804—
Reactant(R)-1-(5-acetoxyhexyl)-8-bromo-7-ethoxymethyl-3-methylxanthineHCID 54041337—
SolventEthanolHCID 702—
ProductHCID 178468220HCID 178468220—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirring solution of (R)-1-(5-acetoxyhexyl)-8-bromo-7-ethoxymethyl-3-methylxanthine (prepared as for CT13430) (1.77 g, 4.0 mmol) in ethanol (100 ml) was added sodium sulfide (4.48 g, 80 mmol). The reaction mixture was stirred at 90° C. for 1 hour. After evaporation of the solvent under reduced pressure, the crude product was purified by flash chromatography on silica gel eluting with ethyl acetate-methanol (7:1) to provide (R)-1-(5-acetoxyhexyl)-7-ethoxymethyl-8-mercapto-3-methylxanthine. This product was dissolved in methanol (100 ml). A solution of hydrogen chloride in ether (1.0 M, 1.0 ml) was added and stirred at room temperature for 24 hours. After evaporation of the solvent under reduced pressure. The crude product was purified by flash chromatography on silica gel eluting with ethyl acetate-methanol (4:1) to provide (R)-7-ethoxymethyl-1-(5-hydroxyhexyl)-8-mercapto-3-methylxanthine (0.61 g, 51% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586429B2
Source datasetuspto-grants-2003_07
ORD IDord-58daaf1746b94eb09eb0d44b88e2cb3f
Source noteuspto-grants-2003_07