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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073159Generated: October 29, 2026

HCID 19828445, compound → 1-[5,5-Bis(4-fluorophenyl)pentyl]-2-piperazinecarboxamide

https://huagongshe.com/reaction/1073159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19828445HCID 19828445—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-[5,5-Bis(4-fluorophenyl)pentyl]-2-piperazinecarboxamideHCID 1508772976.3%

Reaction Steps

A solution of 56.9 parts of 1-[5,5-bis(4-fluorophenyl)-4-pentenyl]-4-(phenylmethyl)-2-piperazinecarboxamide in 400 parts of methanol was hydrogenated in a Parr apparatus and at 50° C. with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated in vacuo. The residue was dissolved in 2-propanone and the whole was acidified with a mixture of hydrochloric acid and 2-propanol. After the addition of 2,2'-oxybispropane, the supernatant liquid was decanted and the precipitate was stirred in 2,2'-oxybispropane. The precipitated product was filtered off and dissolved in water. After washing with 2,2'-oxybispropane, the aqueous layer was treated with ammonium hydroxide and the product was extracted with trichloromethane. The extract was washed with a sodium chloride solution, dried, filtered and evaporated (under trichloromethane), yielding 35.2 parts (76.3%) of 1-[5,5-bis(4-fluorophenyl)pentyl]-2-piperazinecarboxamide as a residue (int. 34).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968684
Source datasetuspto-grants-1990_11
ORD IDord-b0f7cec9f0f3432aa090bb85d0c22795
Source noteuspto-grants-1990_11