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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835727Generated: October 25, 2026

Methyl iodide → 8-Bromo-3,7-dimethyl-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1835727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant8-bromo-3-methyl-3,7-dihydro-1H-purine-2,6-dioneHCID 1548797—
SolventDimethylformamideHCID 6228—
Product8-Bromo-3,7-dimethyl-3,7-dihydro-1H-purine-2,6-dioneHCID 70224293.4%

Reaction Steps

To a stirring suspension of 8-bromo-3-methylxanthine (prepared as described above for CT12440) (12.25 g, 50.0 mmol) and potassium carbonate (8.62 g, 62.5 mmol) in dimethylformamide (150 ml) was added methyl iodide (7.81 g, 55.0 mmol). After stirring overnight at room temperature, the mixture was poured into ice cold water (400 ml) and stirred at 0-5° C. for 1 hour. The precipitate was filtered, rinsed with water (5×25 ml) and dried under vacuum to provide 8-bromo-3,7-dimethylxanthine (12.10 g, 93% yield) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06774130B2
Source datasetuspto-grants-2004_08
ORD IDord-b10c9ede3c1345008b12f267197c0d9e
Source noteuspto-grants-2004_08