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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417799Generated: October 25, 2026

Potassium Carbonate → 2-((6-chloro-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)-4-Fluorobenzonitrile

https://huagongshe.com/reaction/417799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloro-3-methylpyrimidine-2,4(1H,3H)-dioneHCID 96141—
Reactant2-(Bromomethyl)-4-fluorobenzonitrileHCID 21984990—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product2-((6-chloro-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl)-4-FluorobenzonitrileHCID 2308935860%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of crude 3-methyl-6-chlorouracil (5) (0.6 g, 3.8 mmol), 2-Bromomethyl-4-fluorobenzonitrile (0.86 g, 4 mmol) and K2CO3 (0.5 g, 4 mmol) in DMSO (10 mL) was stirred at 60° C. for 2 hours. The reaction was diluted with water and extracted with EtOAc. The organics were dried over MgSO4 and the solvent removed. The residue was purified by column chromatography. 0.66 g of the product was obtained (yield: 60%). 1H-NMR (400 MHz, CDCl3): δ 7.73 (dd, J=7.2, 8.4 Hz, 1H), 7.26 (d, J=4.0 Hz, 1H), 7.11-7.17 (m, 1H), 6.94 (dd, J=2.0, 9.0 Hz, 1H), 6.034 (s, 2H), 3.39 (s, 3H). MS (ES) [m+H] calc'd for C13H9ClFN3O2, 293.68; found 293.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093236B2
Source datasetuspto-grants-2012_01
ORD IDord-9b8385cd5dbe493e8765b9e2e7b38bf2
Source noteuspto-grants-2012_01