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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073156Generated: November 1, 2026

Hydrochloric Acid → 4-[5,5-Bis(4-fluorophenyl)-4-pentenyl]-2-piperazinecarboxamide monohydrate

https://huagongshe.com/reaction/1073156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant7-[5,5-bis(4-fluorophenyl)-4-pentenyl]hexahydro-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-oneHCID 14722547—
Product4-[5,5-Bis(4-fluorophenyl)-4-pentenyl]-2-piperazinecarboxamide monohydrateHCID 2215804850%

Reaction Steps

A mixture of 60 parts of 7-[5,5-bis(4-fluorophenyl)-4-pentenyl]hexahydro-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-one and 850 parts of a hydrochloric acid solution 0.5N was stirred for 2 hours at reflux temperature. After cooling, the reaction mixture was treated with potassium carbonate. The product was extracted with trichloromethane. The extract was dried, filtered and 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 crystallized from 1,1'-oxybisethane. The product was filtered off and dried, yielding 29.5 parts (50%) of 4-[5,5-bis(4-fluorophenyl)-4-pentenyl]-2-piperazinecarboxamide monohydrate; mp. 51.3° C. (int. 25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968684
Source datasetuspto-grants-1990_11
ORD IDord-a4bb263b4e9f42d4b979e7d13488e068
Source noteuspto-grants-1990_11