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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334188Generated: October 30, 2026

Potassium Carbonate → 1-[(3-Cyano-pyridin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-bromo-xanthine

https://huagongshe.com/reaction/334188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant8-Bromo-7-(2-butyn-1-yl)-3,7-dihydro-3-methyl-1H-purine-2,6-dioneHCID 21088927—
Reactant3-Pyridinecarbonitrile, 2-(chloromethyl)-HCID 46911834—
SolventWaterHCID 962—
Product1-[(3-Cyano-pyridin-2-yl)methyl]-3-methyl-7-(2-butyn-1-yl)-8-bromo-xanthineHCID 16726544—

Reaction Conditions

Temperature70 °C

Reaction Steps

202 g (0.68 mol) of 3-methyl-7-(2-butin-1-yl)-8-bromoxanthine, 188.5 g (1.36 mol) of anhydrous potassium carbonate and 1.68 liters of N-methyl-2-pyrrolidone are initially charged in the reactor and heated to 70° C. Subsequently, 119 g (0.75 mol) of 2-chloromethyl-3-cyanopyridine in 240 ml of N-methyl-2-pyrrolidine (NMP) are added dropwise. The reactor contents are stirred at 70° C. for 19 hours. After the reaction has ended, 2.8 liters of water are added to the reaction mixture and it is cooled to 25° C. The product is filtered off, washed with 2 liters of water and dried at 70° C. in a drying cabinet under inertization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883805B2
Source datasetuspto-grants-2014_11
ORD IDord-9e99d6afeca24ca68213790d433cb1ec
Source noteuspto-grants-2014_11