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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723492Generated: October 26, 2026

1,4-Dioxane → 3-[4-[4-(4-Methoxyphenyl)-1-piperazinyl]phenyl]-1-(1-methylethyl)-2,4-imidazolidinedione

https://huagongshe.com/reaction/1723492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantEthyl 2-((propan-2-yl)amino)acetateHCID 351625—
ReactantPhenyl N-(4-(4-(4-methoxyphenyl)piperazin-1-yl)phenyl)carbamateHCID 981607—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product3-[4-[4-(4-Methoxyphenyl)-1-piperazinyl]phenyl]-1-(1-methylethyl)-2,4-imidazolidinedioneHCID 1415293573%

Reaction Steps

A mixture of 5 parts of phenyl [4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]carbamate, 3 parts of ethyl [(1-methylethyl)amino]acetate, 1 part of N,N-dimethyl-4-pyridinamine and 100 parts of 1,4-dioxane was stirred and refluxed overnight. The warm solution was saturated with water and allowed to cool. The solution was poured onto water and extracted with trichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by filtration over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The filtrate was evaporated and the residue was crystalized from methylbenzene, yielding 3.7 parts (73%) of 3-[4-[4-(4-methoxyphenyl)-1-piperazinyl]phenyl]-1-(1-methylethyl)-2,4-imidazolidinedione; mp. 193.7° C. (38).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861879
Source datasetuspto-grants-1989_08
ORD IDord-1df4510d18a141489dbf74c46ad49f0f
Source noteuspto-grants-1989_08