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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35343Generated: October 29, 2026

Ethanol → HCID 14230140, compound

https://huagongshe.com/reaction/35343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThiopheneHCID 8030—
ReactantHCID 14230129HCID 14230129—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 14230140HCID 14230140—

Reaction Steps

To 1 part of a solution of 2 parts of thiophene in 40 parts of ethanol were added 3 parts of 4-[4,4-bis(4-fluorophenyl)butyl]-N-(2,6-dimethyl-4-nitrophenyl)-2-[(methylamino)carbonyl]-1-piperazineacetamide and 120 parts of methanol. The whole was hydrogenated at normal pressure and at room temperature with 2 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. 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 suspended in 2,2'-oxybispropane, yielding 2.14 parts of N-(4-amino-2,6-dimethylphenyl)-4-[4,4-bis(4-fluorophenyl)butyl]-2-[(methylamino)carbonyl]-1-piperazineacetamide; mp. 111.7° C. (compound 162).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-1c2097d3c9d14e7e83bd302cd874adad
Source noteuspto-grants-1988_08