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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428767Generated: November 1, 2026

Pyridine → Phenyl 4-(ethylsulfonamidomethyl)phenylcarbamate

https://huagongshe.com/reaction/1428767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantN-(4-aminobenzyl)ethanesulfonamideHCID 39243426—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl 4-(ethylsulfonamidomethyl)phenylcarbamateHCID 8668022288.7%

Reaction Steps

N-(4-Aminobenzyl)ethanesulfonamide (504 mg, 2.35 mmol) was dissolved in acetonitrile (3 mL) and tetrahydrofuran (4 mL). The reaction mixture was added pyridine (0.23 mL, 2.78 mmol) and phenyl chloroformate (0.31 mL, 2.43 mmol) and stirred at room temperature for 3 h under nitrogen atmosphere. TLC showed complete consumption of starting material. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic part was washed with water and brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography to give phenyl 4-(ethylsulfonamidomethyl)phenylcarbamate (697 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-acd089da99c04ca696f32be790e2eb73
Source noteuspto-grants-2015_01