HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355397Generated: October 26, 2026
Potassium Cyanide → (R)-1-(5-acetoxyhexyl)-7-benzyl-8-cyano-3-methylxanthine
https://huagongshe.com/reaction/1355397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | (R)-1-(5-Acetoxyhexyl)-7-benzyl-8-bromo-3-methylxanthine | HCID 54190334 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (R)-1-(5-acetoxyhexyl)-7-benzyl-8-cyano-3-methylxanthine | HCID 53812008 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06586429B2 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-dd900634b1444fc4913e735fa2e85286 |
|---|
| Source note | uspto-grants-2003_07 |
|---|