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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073189Generated: November 1, 2026

Sodium Carbonate → N-(2-acetylphenyl)-3-(aminocarbonyl)-4-[5,5-bis(4-fluorophenyl)-4-pentenyl]-1-piperazineacetamide

https://huagongshe.com/reaction/1073189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-1,1-bis-(4-fluorophenyl)pent-1-eneHCID 14722550—
ReactantN-(2-acetylphenyl)-3-(aminocarbonyl)-1-piperazineacetamideHCID 15087723—
SolventDimethylformamideHCID 6228—
ProductN-(2-acetylphenyl)-3-(aminocarbonyl)-4-[5,5-bis(4-fluorophenyl)-4-pentenyl]-1-piperazineacetamideHCID 1472267073.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.86 parts of 1,1'-(5-bromo-1-penten-1-ylidene)bis(4-fluorobenzene], 1.50 parts of N-(2-acetylphenyl)-3-(aminocarbonyl)-1-piperazineacetamide, 0.80 parts of sodium carbonate and 90 parts of N,N-dimethylformamide was stirred for 20 hours at 80° C. The reaction mixture was evaporated and the residue was taken up in water. The product was extracted twice with dichloromethane. The combined extracts were washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane, yielding 2.07 parts (73.9%) of N-(2-acetylphenyl)-3-(aminocarbonyl)-4-[5,5-bis(4-fluorophenyl)-4-pentenyl]-1-piperazineacetamide; mp. 110.7° C. (compound 18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968684
Source datasetuspto-grants-1990_11
ORD IDord-a1981ee30ff749f9a0722b35d02ef495
Source noteuspto-grants-1990_11