Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49771Generated: October 26, 2026

4-Aminopyridine → Carbamic acid, 4-pyridinyl-, phenyl ester

https://huagongshe.com/reaction/49771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
SolventDichloromethaneHCID 6344—
ProductCarbamic acid, 4-pyridinyl-, phenyl esterHCID 1140161778.4%

Reaction Steps

To a solution of phenyl chloroformate (5.64 g) in dichloromethane (70 ml) was added a solution of 4-aminopyridine (2.84 g) and triethylamine (5.02 ml) in dichloromethane (100 ml) dropwise under cooling on an ice-water bath. After stirring for 1 hour, the solvents were removed under reduced pressure. A residue was diluted with dichloromethane (200 ml) and water (200 ml). An organic phase was separated and washed with water and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. The reaction mixture was diluted with diisopropyl ether and the precipitates were filtered. After rinse with diethyl ether, O-phenyl N-(4-pyridyl)carbamate (5.07 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-9dacb9240a3644f7b68c0ff696ee87d3
Source noteuspto-grants-2004_03