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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993041Generated: October 31, 2026

Water → Ethyl 4-[[4-[1-(1-Acetoxyethyl)oxycarbonylpiperidin-4-yl]-2-oxopiperazin-1-yl]acetyl]phenoxyacetate

https://huagongshe.com/reaction/993041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantProton spongeHCID 88675—
Reactant1-acetoxyethyl p-nitrophenyl carbonateHCID 11780560—
ReactantHCID 18408903HCID 18408903—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-[[4-[1-(1-Acetoxyethyl)oxycarbonylpiperidin-4-yl]-2-oxopiperazin-1-yl]acetyl]phenoxyacetateHCID 18408908100%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 107 mg of ethyl 4-[[2-oxo-4-(piperidin-4-yl)piperazin-1-yl]acetyl]phenoxyacetate dihydrochloride synthesized according to the method described in WO962503 in 2 ml of N,N-dimethylformamide were added 110 mg of proton sponge and 85.7 mg of 1-acetoxyethyl 4-nitrophenyl carbonate with stirring at 0° C., and the mixture was stirred at room temperature for 18 hours. The reaction mixture was poured into 2 ml of water and extracted three times with 4 ml of ethyl acetate. The organic layer was dried over magnesium sulfate, and the solvent was removed by distillation. The residue thus obtained was purified by chromatography on an LH-20 column (chloroform:methanol=1:1) to give 119 mg of the title compound (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472397B1
Source datasetuspto-grants-2002_10
ORD IDord-c4b5436f4a4144fbb1d2cb1f99bef700
Source noteuspto-grants-2002_10