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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483232Generated: October 25, 2026

Triethylamine → 3-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H,3H)-quinazolinedione

https://huagongshe.com/reaction/483232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiphosgeneHCID 10426—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2-Methoxyphenyl)-4-[2-(2-aminobenzoyl)-aminoethyl]piperazineHCID 57154715—
SolventDichloromethaneHCID 6344—
Product3-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]ethyl]-2,4(1H,3H)-quinazolinedioneHCID 122065—

Reaction Steps

A mixture of 1-(2-methoxyphenyl)-4-[2-(2-aminobenzoyl)-aminoethyl]piperazine (3.54 g) and triethylamine (2.2 g) was dissolved in methylene chloride (50 ml), and the resulting solution was added dropwise to a solution of trichloromethyl chloroformate (0.989 g) in methylene chloride (20 ml) under stirring at between -5° and 5° C. Then, the mixture was gradually heated to room temperature at which it was held for 1 to 2 hours to effect reaction. After completion of the reaction, saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and the resulting mixture was extracted with methylene chloride, the methylene chloride layer was washed with water twice and dried on anhydrous magnesium sulfate. The solvent was concentrated under vacuum and isopropanol was added to the residue to give 2.28 g of crystalline 3-[2-[4-(2-methoxyphenyl)-1-piperazinyl]-ethyl]-2,4-(1H,3H)quinazolinedione having a melting point of 217°-218° C. (recrystallized from chloroform-ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578465
Source datasetuspto-grants-1986_03
ORD IDord-62a9f048b6a045bdbc15ff6899d92e73
Source noteuspto-grants-1986_03