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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421549Generated: October 26, 2026

Potassium Carbonate → methyl 5-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-(3-chloropyridin-2-yl)-2H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/421549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Bis(trifluoromethyl)pyrazoleHCID 518991—
ReactantMethyl 1-(3-chloropyridin-2-yl)-3-{[(methylsulfonyl)oxy]methyl}-1H-pyrazole-5-carboxylateHCID 58320697—
SolventAcetonitrileHCID 6342—
Productmethyl 5-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-(3-chloropyridin-2-yl)-2H-pyrazole-3-carboxylateHCID 86638528—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 700 mg (2.03 mmol) of methyl 2-(3-chloropyridin-2-yl)-5-methane-sulphonyloxymethyl-2H-pyrazole-3-carboxylate in 15 ml of acetonitrile is admixed in succession with 336 mg (2.43 mmol) of potassium carbonate and 413 mg (2.03 mmol) of 3,5-bis(trifluoromethyl)pyrazole and the mixture is subsequently stirred at 60° C. for 1 h. After the mixture has cooled to room temperature, the solvent is concentrated on a rotary evaporator, water is added and extraction is carried out with three times 50 ml of ethyl acetate. The combined organic phases are dried over magnesium sulphate and then the solvent is removed on a rotary evaporator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101550B2
Source datasetuspto-grants-2012_01
ORD IDord-1ef0fe359245463ba40fdfd823310125
Source noteuspto-grants-2012_01