HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 8-bromo-3-methyl-3,7-dihydro-1H-purine-2,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-Benzyl-8-bromo-3-methylxanthine | HCID 836152 | — |
| Reactant | 5-(R)-Acetoxy-1-chlorohexane | HCID 11019434 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 8-bromo-3-methyl-3,7-dihydro-1H-purine-2,6-dione | HCID 1548797 | 167.5% |
Reaction Steps
To a stirring suspension of 7-benzyl-8-bromo-3-methylxanthine (10.06 g, 30.0 mmol) in anhydrous dimethylsulfoxide was added sodium hydride (864 mg, 36.0 mmol). After stirring at room temperature for 30 min, (R)-5-acetoxy-1-chlorohexane (5.9 g, 33.0 mmol) was added. After stirring at 70-75° C. for 12 hours, the mixture was cooled to room temperature, quenched with water (600 ml) and stirred at room temperature for 4 hours. The precipitate was filtered to provide (R)-1-(5-Acetoxyhexyl)-7-benzy)-8-bromo-3-methylxanthine (12.31 g, 86% yield) as a beige powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878715B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-ceba2a662eac47638e9643a1646af8f4 |
| Source note | uspto-grants-2005_04 |