Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520832Generated: October 26, 2026

Potassium Carbonate → 5-nitro-2-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyrimidine

https://huagongshe.com/reaction/1520832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-nitropyrimidineHCID 82544—
Reactant4-(Trifluoromethyl)-1H-pyrazoleHCID 12777795—
SolventAcetonitrileHCID 6342—
Product5-nitro-2-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyrimidineHCID 6815732662%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-chloro-5-nitropyrimidine (1.5 g, 9.4 mmol) and 4-(trifluoromethyl)-1H-pyrazole (1.41 g, 10.3 mmol) in acetonitrile (40 mL) was added potassium carbonate (2.60 g, 18.8 mmol). The reaction was heated to 80° C. and stirred overnight. The reaction was concentrated and the residue was diluted with water and extracted with ethyl acetate (2×40 mL). The combined organics were washed with brine, dried over sodium sulfate, filtered, and concentrated. Purification by flash column chromatography gave 5-nitro-2-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyrimidine (1.5 g, 62%) as a yellow solid. 1H NMR (400 MHz, CDCl3, δ): 9.48 (s, 2H), 8.92 (s, 1H), 8.05 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073871B2
Source datasetuspto-grants-2015_07
ORD IDord-c506acbf015c4108b348dbe10ceb8f89
Source noteuspto-grants-2015_07