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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638643Generated: October 30, 2026

Potassium Iodide → HCID 14722574, compound

https://huagongshe.com/reaction/1638643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 14722540HCID 14722540—
Reactant1,1'-(5-Chloropentylidene)bis(4-fluorobenzene)HCID 15087714—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 14722574HCID 14722574—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3.5 parts of 1,1'-(5-chloro-1-pentylidene)bis[4-fluorobenzene], 2.94 parts of 3-(aminocarbonyl)-N-(5-fluoro-2-methylphenyl)-1-piperazineacetamide, 2.1 parts of N,N-diethylethanamine, 0.1 parts of potassium iodide and 45 parts of N,N-dimethyformamide was stirred and heated for 48 hours at about 70° C. After 24 hours of stirring 2.12 parts of sodium carbonate were added. The reaction mixture was evaporated. The residue was taken up in water and the product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the hydrochloride salt in acetonitrile, 2-propanol and a few drops of water. The salt was filtered off and dried over weekend at 100° C., yielding 1.70 parts of 3-(aminocarbonyl)-4-[5,5-bis(4-fluorophenyl)pentyl] -N-(5-fluoro-2-methylphenyl)-1-piperazineacetamide monohydrochloride; mp. 217.8° C. (compound 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880808
Source datasetuspto-grants-1989_11
ORD IDord-5b063f04c2ed4321af8527f8c33b7c57
Source noteuspto-grants-1989_11