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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433716Generated: October 25, 2026

Potassium Carbonate → 2,5-Difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene

https://huagongshe.com/reaction/433716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2,4-Trifluoro-5-nitrobenzeneHCID 75012—
Reactant1-Methyl-6-trifluoromethylpyrimidine-2,4-dioneHCID 11435480—
SolventDimethyl SulfoxideHCID 679—
Product2,5-Difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzeneHCID 1211550943%

Reaction Conditions

Temperature80 °C

Reaction Steps

1.77 g of 2,4,5-trifluoronitrobenzene and 1.94 g of 3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidine were dissolved in 10 ml of dimethyl sulfoxide, and 1.52 g of anhydrous potassium carbonate was added to this at room temperature, then, the mixture was stirred for 1 hour at 80° C. The reaction solution was allowed to cool to room temperature, then, the reaction solution was poured into ice water, and extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 1.51 g of 2,5 difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667413B2
Source datasetuspto-grants-2003_12
ORD IDord-1294542146784e74bd5271fc17b79bb0
Source noteuspto-grants-2003_12