Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49776Generated: October 26, 2026

1-Acetylpiperazine → 1-Acetyl-4-(4-pyridylaminocarbonyl)piperazine

https://huagongshe.com/reaction/49776

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantCarbamic acid, 4-pyridinyl-, phenyl esterHCID 11401617—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Acetyl-4-(4-pyridylaminocarbonyl)piperazineHCID 988138977%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of O-phenyl N-(4-pyridyl)carbamate (446 mg) in 1,2-dichloroethane (5 ml) was added a suspension of 1-acetylpiperazine (1.12 g) in 1,2-dichloroethane (20 ml) at ambient temperature. The mixture was heated at 60° C. with stirring for 9 hours. The mixture was cooled to ambient temperature, and diluted with dichloromethane and water. The aqueous phase was separated and adjusted to pH 11.5 with sodium hydroxide solution. Excess sodium chloride was added to the aqueous solution. The mixture was extracted with a mixture of dichloromethane and methanol (about 10:1) and the organic phase was washed with brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. A residue was purified by column chromatography (silica gel 100 ml, dichloromethane:methanol aqueous ammonia=10:1:0.1). After rinse with diisopropyl ether, 1-acetyl-4-(4-pyridylaminocarbonyl)piperazine (398 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-16e740a395d64bbcae2ab6ec1d8a13fb
Source noteuspto-grants-2004_03