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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537490Generated: October 26, 2026

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

https://huagongshe.com/reaction/537490

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 6815732649%

Reaction Conditions

Temperature80 °C

Reaction Steps

A round bottom flask was charged with 2-chloro-5-nitropyrimidine (2.50 g, 15.7 mmol), 4-(trifluoromethyl)-1H-pyrazole (2.35 g, 17.2 mmol), K2CO3 (4.33 g, 31.3 mmol) and acetonitrile (39 mL). The reaction was heated at 80° C. for 2 hours. Potassium carbonate filtered off with a büchner funnel and acetonitrile removed under reduced pressure. The crude material was dissolved in ethyl acetate and transferred to a separatory funnel. Organics washed with water (3×), with brine (1×), dried over sodium sulfate, filtered and concentrated to afford the raw material. Purification by silica gel flash chromatography (ethyl acetate/heptane) provide 5-nitro-2-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyrimidine (1.95 g, 49%) as a yellow solid. MS (M+1): 259.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859591B2
Source datasetuspto-grants-2014_10
ORD IDord-65cfc85a93b442039175e7582c2fe8f6
Source noteuspto-grants-2014_10