Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428710Generated: November 1, 2026

Pyridine → Phenyl 4-(methylsulfonamidomethyl)phenylcarbamate

https://huagongshe.com/reaction/1428710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantN-[(4-aminophenyl)methyl]methanesulfonamideHCID 12822521—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductPhenyl 4-(methylsulfonamidomethyl)phenylcarbamateHCID 8667936478%

Reaction Steps

N-(4-Aminobenzyl)methanesulfonamide (352 mg, 1.76 mmol) was dissolved in acetonitrile (3 mL) and tetrahydrofuran (4 mL). The reaction mixture was added pyridine (0.17 mL, 2.11 mmol) and phenyl chloroformate (0.23 mL, 1.85 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-(methylsulfonamidomethyl)phenylcarbamate (438 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-cddda5fa52204ba8907dfc7959d86be5
Source noteuspto-grants-2015_01