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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428763Generated: November 2, 2026

Phenyl 3-methyl-4-(methylsulfonamidomethyl)phenylcarbamate → N-(2-Methyl-4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide

https://huagongshe.com/reaction/1428763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl 3-methyl-4-(methylsulfonamidomethyl)phenylcarbamateHCID 86679391—
Reactant(2-m-Tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamineHCID 86680208—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductN-(2-Methyl-4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamideHCID 7153938588%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of phenyl 3-methyl-4-(methylsulfonamidomethyl)-phenylcarbamate (46 mg, 0.137 mmol) and (2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methanamine (36 mg, 0.137 mmol) in acetonitrile were added 4-dimethylaminopyridine (17 mg, 0.137 mmol). The reaction mixture was stirred for 15 h at 50° C. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(2-Methyl-4-(3-((2-m-tolyl-6-(trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)methanesulfonamide (example 81) (61 mg) was obtained as 88% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-635cbed2a88e42bab6d761519e7c6340
Source noteuspto-grants-2015_01