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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009482Generated: October 30, 2026

Potassium Carbonate → N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)-N2-[(4-fluorophenyl)sulfonyl]glycinamide

https://huagongshe.com/reaction/1009482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(3-chloro-2-methylphenyl)-4-fluorobenzenesulfonamideHCID 711089—
Reactant2-Bromo-N-(4-methoxybenzyl)acetamideHCID 46736691—
SolventDimethylformamideHCID 6228—
ProductN2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)-N2-[(4-fluorophenyl)sulfonyl]glycinamideHCID 5800967765.2%

Reaction Steps

449 mg of N-(3-chloro-2-methylphenyl)-4-fluorobenzenesulfonamide was dissolved in 3.00 mL of DMF, and 387 mg of 2-bromo-N-(4-methoxybenzyl)acetamide and 207 mg of potassium carbonate were added thereto, followed by stirring at room temperature overnight. To the reaction liquid was added an aqueous sodium hydrogen carbonate solution, followed by extraction with chloroform, and the organic layer was washed with brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate) to obtain a product, which was crystallized from hexane/ethyl acetate to obtain 466 mg of N2-(3-chloro-2-methylphenyl)-N-(4-methoxybenzyl)-N2-[(4-fluorophenyl)sulfonyl]glycinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973078B2
Source datasetuspto-grants-2011_07
ORD IDord-68157fb626c643b98a7a41f6861b1386
Source noteuspto-grants-2011_07