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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35341Generated: October 27, 2026

Potassium Iodide → HCID 14230181, compound

https://huagongshe.com/reaction/35341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant3-Chloro-2',6'-propionoxylidideHCID 4550832—
Reactant1-[4,4-Bis(4-fluorophenyl)butyl]-2-piperazinecarboxamideHCID 13883288—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductHCID 14230181HCID 1423018170.8%

Reaction Steps

A mixture of 3.7 parts of 1-[4,4-bis(4-fluorophenyl)butyl]-2-piperazinecarboxamide, 2.3 parts of 3-chloro-N-(2,6-dimethylphenyl)propanamide, 2.1 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone was stirred and refluxed for 20 hours using a water-separator. The reaction mixture was cooled to room temperature and filtered. The filtrate was evaporated. The oily 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 solidified on triturating in 2,2'-oxybispropane. The product was filtered off and dried, yielding 3.87 parts (70.8%) of 3-(aminocarbonyl)-4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethylphenyl)-1-piperazinepropanamide; mp. 120.9° C. (compound 122)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-78494dc96eda43ba92e7924d4d4763f5
Source noteuspto-grants-1988_08