HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842540Generated: 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/1842540
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Bis(trifluoromethyl)pyrazole | HCID 518991 | — |
| Reactant | Methyl 1-(3-chloropyridin-2-yl)-3-{[(methylsulfonyl)oxy]methyl}-1H-pyrazole-5-carboxylate | HCID 58320697 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | methyl 5-(3,5-bistrifluoromethylpyrazol-1-ylmethyl)-2-(3-chloropyridin-2-yl)-2H-pyrazole-3-carboxylate | HCID 86638528 | — |
Reaction Steps
A solution of 700 mg (2.03 mmol) of methyl 2-(3-chloropyridin-2-yl)-5-methanesulphonyloxymethyl-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946236B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b16e0e6205fe43ed9641d817c1defbd5 |
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| Source note | uspto-grants-2015_02 |
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