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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208005Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 118432066, compound

https://huagongshe.com/reaction/2208005

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 118431847HCID 118431847—
SolventDichloromethaneHCID 6344—
ProductHCID 118432066HCID 11843206638.9%

Reaction Steps

To a mixture of 1-(2-chloro-phenyl)-5-[2-(4-methylsulfanyl-phenyl)-pyridin-6-yl]-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (9.0 mg, 0.02 mmol) prepared in Example 153 in dichloromethane (1.0 mL), was slowly added meta-chloroperbenzoic acid (77%, 2.0 mg, 0.01 mmol) at 0° C. The reaction mixture was stirred at room temperature for 30 minutes, quenched with a saturated solution of sodium hydrogen carbonate, and then extracted with dichloromethane three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a yellow liquid residue. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=3/1) to give 2.0 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-459eb65d7cd3496e99de8d2ec6b24e47
Source noteuspto-grants-2016_06