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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185822Generated: October 31, 2026

Sodium Carbonate → 4-[4,4-bis(4-fluorophenyl)butyl]-3-[(methylamino)-carbonyl]-N-(2,4,6-trimethylphenyl)-1-piperazineacetamide

https://huagongshe.com/reaction/2185822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1,1'-(4-Iodobutylidene)bis[4-fluorobenzene]HCID 103968—
Reactant3-[(methylamino)carbonyl]-N-(2,4,6-trimethylphenyl)-1-piperazineacetamideHCID 14230235—
SolventDimethylformamideHCID 6228—
Product4-[4,4-bis(4-fluorophenyl)butyl]-3-[(methylamino)-carbonyl]-N-(2,4,6-trimethylphenyl)-1-piperazineacetamideHCID 1423008246%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 6.7 g of 1,1′-(4-iodobutylidene)bis[4-fluorobenzene], 5.2 g of 3-[(methylamino)carbonyl]-N-(2,4,6-trimethylphenyl)-1-piperazineacetamide, 2.3 g sodium carbonate and 38 ml DMF is stirred for 18 hours at 70° C. The reaction mixture is cooled and poured onto ice-water. The product is extracted with DCM. The extract is washed with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is dried, yielding 4.23 g of 4-[4,4-bis(4-fluorophenyl)butyl]-3-[(methylamino)-carbonyl]-N-(2,4,6-trimethylphenyl)-1-piperazineacetamide (compound 1, mp. 82.3° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403589B1
Source datasetuspto-grants-2002_06
ORD IDord-2a9e7fa9d2b74b178549c9d01854638d
Source noteuspto-grants-2002_06