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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727023Generated: October 26, 2026

Potassium Carbonate → 8-bromo-7-(2-chloro-6-fluorobenzyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/1727023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBromotheophyllineHCID 11808—
Reactant2-Chloro-6-fluorobenzyl bromideHCID 2773625—
ReactantPotassiumHCID 5462222—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product8-bromo-7-(2-chloro-6-fluorobenzyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dioneHCID 65923589%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 8-bromotheophylline (10 g, 39 mmol) in 30 mL water was treated with potassium carbonate (2.6 g, 48 mmol). The reaction mixture was refluxed until dissolved. Ethanol (30 mL) was added to the hot reaction mixture and the resulting potassium salt was filtered, washed with acetone, and dried in a 100° C. vacuum oven. A solution of 2-chloro-6-fluorobenzyl bromide (5.3 g, 24 mmol) in 10 mL DMSO was treated with the solid potassium salt The reaction mixture was heated to 100° C. for 1 hour and cooled. Upon addition of 5 mL water, the mixture was collected by filtration and dried in a vacuum oven to yield a white solid (6.0 g, 89% yield): 1H NMR (CDCl3, 300 MHz) 7.37-7.21 (m, 2H), 7.07-6.96 (m, 1H), 5.87 (s, 2H), 3.60 (s, 3H), 3.42 (s, 3H); MS (ESP+) m/e 402 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495004B2
Source datasetuspto-grants-2009_02
ORD IDord-e5679d5a013c4af3a4c01a9eec0b48db
Source noteuspto-grants-2009_02