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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729289Generated: November 1, 2026

Triethylamine → HCID 9823946, compound

https://huagongshe.com/reaction/1729289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(3-Bromopropoxy)-4-chlorobenzeneHCID 223534—
Reactant1,3-Dimethyl-6-(piperazin-1-yl)pyrimidine-2,4(1H,3H)-dioneHCID 12816873—
SolventEthanolHCID 702—
ProductHCID 9823946HCID 982394686.1%

Reaction Steps

3 ml of triethylamine was added to 10 ml of an ethanol solution containing 2.5 g of 3-(4-chlorophenoxy)propyl bromide and 1.3 g of 1,3-dimethyl-6-(1-piperazinyl)-2,4(1H,3H)-pyrimidinedione, and the solution was then heated under reflux for 3 hours. Afterward, the reaction solution was concentrated to dryness, and the resultant residue was dissolved in chloroform and then washed with water. The thus obtained chloroform solution was dried and then concentrated, and the residue was recrystallized from ethanol/hexane, thereby preparing 1.96 g (yield: 86%) of 6-[4-(3-[4-chlorophenoxy]propyl)piperazin-1-yl]-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332739
Source datasetuspto-grants-1994_07
ORD IDord-e3b52a76561d41cd97afe2cec71b36c4
Source noteuspto-grants-1994_07