HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835707Generated: October 27, 2026
Sodium hydride → (R)-1-(5-acetoxyhexyl)-3-(2-furylmethyl)-7-methylxanthine
https://huagongshe.com/reaction/1835707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(2-Furylmethyl)-7-methylxanthine | HCID 22499127 | — |
| Reactant | (R)-5-acetoxy-1-iodohexane | HCID 54009360 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (R)-1-(5-acetoxyhexyl)-3-(2-furylmethyl)-7-methylxanthine | HCID 54209961 | 78% |
Reaction Steps
To a stirring suspension 3-(2-furylmethyl)-7-methylxanthine (0.40 g, 1.62 mmol) in dimethylsulfoxide (20 ml) was added sodium hydride (41 mg, 1.71 mmol) in one portion. After stirring for 25 minutes, (R)-5-acetoxy-1-iodohexane (0.46 g, 1.71 mol) was added neat. After stirring at room temperature for 72 hours, the reaction was quenched by the addition of water (75 ml) and extracted with ethyl acetate (3×35 ml). The combined extracts were washed with saturated aqueous sodium chloride solution (2×35 ml), dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate to give (R)-1-(5-acetoxyhexyl)-3-(2-furylmethyl)-7-methylxanthine (0.49 g, 78% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06774130B2 |
|---|
| Source dataset | uspto-grants-2004_08 |
|---|
| ORD ID | ord-5f1e9170d59f41fe81d1a9109cadb681 |
|---|
| Source note | uspto-grants-2004_08 |
|---|