HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35330Generated: October 29, 2026
Hydrochloric Acid → 4-[4,4-bis(4-fluorophenyl)butyl]-N-(2-hydroxyethyl)-2-piperazinecarboxamide
https://huagongshe.com/reaction/35330
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 7-[4,4-bis(4-fluorophenyl)butyl]hexahydro-2-(2-hydroxyethyl)-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-one | HCID 21295647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[4,4-bis(4-fluorophenyl)butyl]-N-(2-hydroxyethyl)-2-piperazinecarboxamide | HCID 21295690 | 100% |
Reaction Steps
A mixture of 40 parts of 7-[4,4-bis(4-fluorophenyl)butyl]hexahydro-2-(2-hydroxyethyl)-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-one, 19 parts of hydrochloric acid solution 10.5N and 400 parts of water was stirred for one hour in a boiling water-bath on a Rotavapor. After cooling, the reaction mixture was washed twice with 140 parts of 1,1'-oxybisethane. The aqueous phase was alkalized with ammonium hydroxide. The product was extracted twice with 140 parts of 1,1'-oxybisethane. The combined extracts were dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using first a mixture of trichloromethane and methanol (90:10 by volume) and then a mixture of trichloromethane and methanol saturated with ammonia (90:10 by volume) as eluents. The pure fractions were collected and the eluent was evaporated, yielding 33.7 parts (100%) of 4-[4,4-bis(4-fluorophenyl)butyl]-N-(2-hydroxyethyl)-2-piperazinecarboxamide (intermediate 95).
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-59b6a0da634944dc812997da1485cb39 |
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| Source note | uspto-grants-1988_08 |
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