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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291192Generated: October 30, 2026

Sodium Iodide → 6-{4-[4-(2-Chloro-6-methlphenyl)-1-piperazinyl]-1-butenyl}-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/2291192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2-Chloro-6-methylphenyl)piperazineHCID 14624995—
Reactant6-(4-Chloro-1-butenyl)-3,4-dihydrocarbostyrilHCID 54437579—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product6-{4-[4-(2-Chloro-6-methlphenyl)-1-piperazinyl]-1-butenyl}-3,4-dihydrocarbostyrilHCID 54092414—

Reaction Conditions

Temperature50 °C

Reaction Steps

2.8 Grams of 6-(4-chloro-1-butenyl)-3,4-dihydrocarbostyril and 2.1 g of sodium iodide were dissolved in 40 ml of dimethylformamide and stirred at 50° C. for 1 hour. To this solution were added 2.7 g of 4-(2-chloro-6-methylphenyl)piperazine and 1.5 g of triethylamine and the mixture was further stirred at 50° C. for 5 hours. 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 to precipitate crystals. The crystals were separated by a silica-gel chromatography and recrystallized from ethanol-acetone-chloroform to obtain 6-{4-[4-(2-chloro-6-methylphenyl)-1-piperazinyl]-1-butenyl}-3,4-dihydrocarbostyril in colorless prism-like crystals. Yield: 2.7 g. Melting point: 179°-180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04619932
Source datasetuspto-grants-1986_10
ORD IDord-c8eba11caf46408789576d714decac5f
Source noteuspto-grants-1986_10