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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35336Generated: October 26, 2026

Potassium Iodide → 3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)pentyl]-N-(2,6-dichlorophenyl)-1-piperazineacetamide dihydrochloride monohydrate

https://huagongshe.com/reaction/35336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-Carbamoyl-N-(2,6-dichlorophenyl)piperazine-1-acetamideHCID 14230231—
Reactant1,1'-(5-Chloropentylidene)bis(4-fluorobenzene)HCID 15087714—
SolventMethyl Isobutyl KetoneHCID 7909—
Product3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)pentyl]-N-(2,6-dichlorophenyl)-1-piperazineacetamide dihydrochloride monohydrateHCID 86742389—

Reaction Steps

A mixture of 5 parts of 1,1'-(5-chloropentylidene)bis(4-fluorobenzene), 5 parts of 3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-1-piperazineacetamide, 2.2 parts of sodium carbonate, 0.1 parts of potassium iodide and 120 parts of 4-methyl-2-pentanone was stirred and refluxed for 24 hours. The reaction mixture was cooled and purified by column-chromatography (2x) over silica gel using first a mixture of trichloromethane and methanol (95:5 by volume) and then a mixture of trichloromethane and methanol (97:3 by volume) as eluents. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in acetonitrile and 2-propanol. After stirring for one hour at room temperature, the salt was filtered off and dried, yielding 1.53 parts of 3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)pentyl]-N-(2,6-dichlorophenyl)-1-piperazineacetamide dihydrochloride monohydrate; mp. 206.2° C. (compound 49).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-88d463e497774174bbe53dcf131560d6
Source noteuspto-grants-1988_08