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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547763Generated: October 31, 2026

Methanol → 2-(3,5-Bis-trifluoromethyl-phenyl)-n-[4-(2-chloro-phenyl)-6-(2-methanesulfonyl-ethylamino)-pyridin-3-yl]-n-methyl-isobutyramide

https://huagongshe.com/reaction/547763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium caroateHCID 15793144—
Reactant2-(3,5-Bis-trifluoromethyl-phenyl)-n-[4-(2-chloro-phenyl)-6-(2-methylsulfanyl-ethylamino)-pyridin-3-yl]-n-methyl-isobutyramideHCID 87305995—
Product2-(3,5-Bis-trifluoromethyl-phenyl)-n-[4-(2-chloro-phenyl)-6-(2-methanesulfonyl-ethylamino)-pyridin-3-yl]-n-methyl-isobutyramideHCID 1127358455%

Reaction Steps

A mixture of 50 mg (0.087 mmol) 2-(3,5-bis-trifluoromethyl-phenyl)-N-[4-(2-chloro-phenyl)-6-(2-methylsulfanyl-ethylamino)-pyridin-3-yl]-N-methyl-isobutyramide and 130 mg (0.212 mmol) potassium monopersulfate triple salt in 1 ml methanol was stirred at room temperature for 3 days. The reaction was quenched with 1 ml sodium hydrogen sulfite solution 38%. The mixture was treated with 3 ml saturated sodium carbonate solution and extracted with three 5-ml portions of ethyl acetate. The combined organic layers were dried over sodium sulfate, concentrated in vacuo and purified by flash chromatography to give 29 mg (55%) of the title compound as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939533B2
Source datasetuspto-grants-2011_05
ORD IDord-dfe2d9c0c1a440f399c57df11f4c4eb0
Source noteuspto-grants-2011_05