Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984815Generated: October 26, 2026

Potassium Iodide → 8-Chloro-7-(2-iodobenzyl)-1,3-dimethyl-3,7-dihydropurine-2,6-dione

https://huagongshe.com/reaction/984815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant8-ChlorotheophyllineHCID 10661—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Chloromethyl)-2-iodobenzeneHCID 101064—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product8-Chloro-7-(2-iodobenzyl)-1,3-dimethyl-3,7-dihydropurine-2,6-dioneHCID 22508626—

Reaction Steps

8-Chlorotheophylline (8.5 g, 39.6 mmol) was dissolved in 400 ml of DMF and 2-iodobenzyl chloride (10.0 g, 39.6 mmol), potassium carbonate (5.47 g, 39.6 mmol), and potassium iodide (10 mg, 0.06 mmol) were added. The mixture was stirred at room temperature for 7 days. Water (2500 ml) and EtOAc (800 ml) were added and the layers were separated. The aqueous layer was extracted with 2×500 ml of EtOAc, and the combined organic layer was washed with 500 ml of water, 500 ml of brine, dried over sodium sulphate, and filtered. The solvent was evaporated and the crude product was crystallized from diethyl ether and petrol, to give compound (5A) as white crystals. The mother liquor was evaporated and resuspended in diethyl ether and petrol, to give a second crop of compound (5A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06869947B2
Source datasetuspto-grants-2005_03
ORD IDord-0554b8ada92042d794c0106cc4369542
Source noteuspto-grants-2005_03