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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570764Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 89488421, compound

https://huagongshe.com/reaction/570764

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 71547715HCID 71547715—
SolventDichloromethaneHCID 6344—
ProductHCID 89488421HCID 89488421—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of N-[3-[[2,6-dibromo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-methyl-carbamoyl]-2-methoxy-phenyl]-N-methyl-pyridine-4-carboxamide (Example G-17) (0.051 g, 0.073 mmole) in dichloromethane (0.44 ml) was added by small portions 3-chloroperbenzoic acid (purity 70%) (0.027 g, 0.11 mmole). After 2.5 hours stirring at 25° C., the yellow solution was quenched with aqueous sodium sulfite, diluted with dichloromethane and washed twice with saturated aqueous sodium bicarbonate, then with brine. The organic solution was dried over sodium sulfate. The product (Compound G18 of Table G) was isolated after removal of the solvent, as a white powder (melting range: 105-194° C.) showing, by LC-MS analysis (method 6 described hereunder) a retention time of 0.99 min and a M+H+ peak of 716.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023873B2
Source datasetuspto-grants-2015_05
ORD IDord-649c246f0e29467595ef3cad8f6deb7d
Source noteuspto-grants-2015_05