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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738352Generated: October 27, 2026

Pyrazole → HCID 15451767, compound

https://huagongshe.com/reaction/1738352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-3-fluoro-4-methylsulfonylbenzoic acidHCID 15451759—
SolventDimethylformamideHCID 6228—
ProductHCID 15451767HCID 15451767—

Reaction Conditions

Temperature50 °C

Reaction Steps

Pyrazole (210 mg, 3.09 mmol) was added to 190 mg (4.75 mmol) of 60 percent oil dispersed sodium hydride suspended in 7 mL of dry dimethylformamide. After the gas evolution had subsided, 500 mg (1.98 mmol) of 2-chloro-3-fluoro-4-methylsulfonylbenzoic acid was added and the mixture was stirred at 50° C. overnight. The mixture was then concentrated by evaporation under reduced pressure and the residue was partitioned between ethyl acetate and 1N aqueous hydrochloric acid. The aqueous phase was extracted with ethyl acetate. The organic phases were combined and extracted with dilute aqueous sodium bicarbonate solution. The aqueous extract was acidified with 1N aqueous hydrochloric acid and extracted with dichloromethane. The organic extract was concentrated by evaporation under reduced pressure. The crystalline residue obtained was purified by rinsing with ethyl acetate to obtain 540 mg (91 percent of theory) of the title compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962690
Source datasetuspto-grants-1999_10
ORD IDord-f0121fcb9fe84c20ad7f5e51c665b6c7
Source noteuspto-grants-1999_10