Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648487Generated: October 25, 2026

1,4-Dioxane → HCID 14152935, compound

https://huagongshe.com/reaction/648487

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—
ProductHCID 14152935HCID 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 crystallized 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 numberUS04735942
Source datasetuspto-grants-1988_04
ORD IDord-be92ae4a412444b888a6a9a14e4eb534
Source noteuspto-grants-1988_04