HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35345Generated: October 29, 2026
3-(aminocarbonyl)-4-[3,3-bis(4-fluorophenyl)-2-propenyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide → 3-(aminocarbonyl)-4-[3,3-bis(4-fluorophenyl)propyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide
https://huagongshe.com/reaction/35345
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(aminocarbonyl)-4-[3,3-bis(4-fluorophenyl)-2-propenyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide | HCID 54542281 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(aminocarbonyl)-4-[3,3-bis(4-fluorophenyl)propyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide | HCID 14230224 | — |
Reaction Steps
A mixture of 4 parts of 3-(aminocarbonyl)-4-[3,3-bis(4-fluorophenyl)-2-propenyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide and 120 parts of methanol 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 (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was suspended in 2,2'-oxybispropane. The product was filtered off and dissolved in acetonitrile. The solution was filtered and the filtrate was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 2.21 parts of 3-(aminocarbonyl)-4-[3,3-bis(4-fluorophenyl)propyl]-N-(2,6-dimethylphenyl)-1-piperazineacetamide; mp. 143.2° C. (compound 170).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766125 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-ad69b0e3e4624553a779d887e44f7b5b |
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| Source note | uspto-grants-1988_08 |
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