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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662597Generated: October 29, 2026

Potassium Carbonate → 5-chloro-3-hydroxy-3-(2-methoxyphenyl)-1-{[4-methoxy-2-(trifluoromethoxy)phenyl]sulfonyl}-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1662597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-oneHCID 21905955—
Reactant4-Methoxy-2-(trifluoromethoxy)benzene sulfonyl chlorideHCID 86625684—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product5-chloro-3-hydroxy-3-(2-methoxyphenyl)-1-{[4-methoxy-2-(trifluoromethoxy)phenyl]sulfonyl}-1,3-dihydro-2H-indol-2-oneHCID 6742985048.5%

Reaction Steps

Under nitrogen atmosphere, to a solution of 5.00 g of 5-chloro-3-hydroxy-3-(2-methoxyphenyl)-1,3-dihydro-2H-indol-2-one, which is the compound described in Preparation 1.1A of brochure Publication No. WO01/5513,0 in DMF (50 ml) was added 760 mg of NaH under ice cooling, then, the reaction mixture was warmed to room temperature and stirred for 30 minutes. To the stirred solution, under cooling at −20° C., was added dropwise a solution of 5.52 g of 4-methoxy-2-(trifluoromethoxy)benzene sulfonyl chloride in DMF (10 ml) over 3 minutes, then, the solution was stirred at the same temperature for 5 hours. After warming to 0° C., to the reaction solution was added CHCl3 and an aqueous solution of 5% K2CO3, and the solution was stirred at room temperature for 30 minutes. The liquid separation of the stirred solution was performed, then the aqueous layer was extracted with CHCl3, the combined organic layer was washed with saturated brine, dried over MgSO4, then, the drying agent was separated by filtration, and was solvent under reduced pressure. The obtained residue was purified by column chromatography (silicagel 60; mobile phase: EtOAc/n-hexane=1/1; v/v) to obtain 4.55 g of the title compound (orange color solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030499B2
Source datasetuspto-grants-2011_10
ORD IDord-ab113497c83740e4be7c73a4770d67c7
Source noteuspto-grants-2011_10