Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993054Generated: November 4, 2026

1-(2-Hydroxyethyl)piperazine → 5-[3-(4-Methoxyphenyl)propyl]-5-[4-(2-hydroxyethyl)piperazinyl]barbituric Acid

https://huagongshe.com/reaction/993054

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
Reactant5-Bromo-5-[3-(4-methoxyphenyl)propyl]barbituric acidHCID 18408679—
SolventEthanolHCID 702—
Product5-[3-(4-Methoxyphenyl)propyl]-5-[4-(2-hydroxyethyl)piperazinyl]barbituric AcidHCID 184086743.7%

Reaction Steps

A of 5-Bromo-5-[3-(4-Methoxyphenyl)propyl]barbituric Acid (710 mg) and N-(2-hydroxyethyl)piperazine (281 mg) in 25 ml of ethanol is refluxed for 4 hours. The solvent is evaporated under reduced pressure and the residue is partitioned between 1 N hydrochloric acid and ethyl acetate. The aqueous phase is basified to pH=6-7 and extracted with ethyl acetate. The organic phase is concentrated to dryness and the residue is crystallized from ethyl acetate to give 30 mg of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472396B1
Source datasetuspto-grants-2002_10
ORD IDord-06b3964bb09e48b6a4ec998ca2b1d46c
Source noteuspto-grants-2002_10