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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285448Generated: October 27, 2026

Hydrochloric Acid → 6-{4-[4-(3-Chlorophenyl)-1-piperazinyl]-1-butenyl}-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1285448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
Reactant2(1H)-Quinolinone, 3,4-dihydro-6-(4-(4-(3-chlorophenyl)-1-piperazinyl)-1-hydroxybutyl)-HCID 3067079—
SolventAcetic AcidHCID 176—
Product6-{4-[4-(3-Chlorophenyl)-1-piperazinyl]-1-butenyl}-3,4-dihydrocarbostyrilHCID 54568797—

Reaction Conditions

Temperature80 °C

Reaction Steps

1.9 Grams of 6-{1-hydroxy-4-[4-(3-chlorophenyl)-1-piperazinyl]butyl}-3,4-dihydrocarbostyril was dissolved in 50 ml of acetic acid and further 2 ml of concentrated hydrochloric acid was added to this solution. The solution was stirred at 80° C. for 30 minutes and the reaction mixture was concentrated under a reduced pressure to dryness to obtain a residue. To the residue were added 10N-NaOH and ether and stirred at a room temperature for 30 minutes. The crystals thus precipitated were collected by filtration and separated by a silica-gel chromatography. Recrystallized from ethanol-chloroform to obtain 6-{4-[4-(3-chlorophenyl)-1-piperazinyl]-1-butenyl}-3,4-dihydrocarbostyril in colorless prism-like crystals. Yield: 1.6 g. Melting point: 175°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567187
Source datasetuspto-grants-1986_01
ORD IDord-b5ec8cdc16ab48c3b8761c781ff4d647
Source noteuspto-grants-1986_01