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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984812Generated: October 26, 2026

Potassium Iodide → 2-(8-Chloro-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-ylmethyl)benzonitrile

https://huagongshe.com/reaction/984812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant8-ChlorotheophyllineHCID 10661—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Bromomethyl)benzonitrileHCID 89599—
SolventDimethylformamideHCID 6228—
Product2-(8-Chloro-1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-ylmethyl)benzonitrileHCID 8850980—

Reaction Steps

8-Chlorotheophylline (20 g, 93.19 mmol) was dissolved in 800 ml of DMF and 2-cyanobenzyl bromide (18.28 g, 93.19 mmol), potassium carbonate (12.88 g, 93.19 mmol), and potassium iodide (10 mg, 0.06 mmol) were added. The mixture was stirred at room temperature for 20 hours. The solvent was evaporated and the residue was suspended in 900 ml of water and 900 ml of EtOAc, and compound (1A) was collected by filtration of the suspension. The layers in the mother liquor were separated and the aqueous layer was extracted with 3×500 ml of EtOAc. The combined organic layers were washed with 1×500 ml of water, and the solvent was evaporated to give compound (1A) as white crystals. Combined yield: 28.6 g (93%). Mp. 222.5-223.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06869947B2
Source datasetuspto-grants-2005_03
ORD IDord-c37d1046755e4e23af97b0d53608881c
Source noteuspto-grants-2005_03