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HRID 621559Erstellt: 26. Oktober 2026

Hydrochloric Acid → 7-{3-[4-(3,4,5-Trimethoxyphenyl)-piperazinyl]propoxy}-3,4-dihydrocarbostyril dihydrochloride

https://huagongshe.com/reaction/621559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
EduktSodium BicarbonateHCID 516892—
Edukt1-(3,4,5-Trimethoxyphenyl)piperazineHCID 3838765—
Edukt3-Chloropropoxy-3,4-dihydrocarbostyrilHCID 131715924—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelPyridineHCID 1049—
Produkt7-{3-[4-(3,4,5-Trimethoxyphenyl)-piperazinyl]propoxy}-3,4-dihydrocarbostyril dihydrochlorideHCID 1289952661%

Reaktionsschritte

12.4 grams of 7-(3-chloropropoxy-3,4-dihydrocarbostyril, 1 g of pyridine and 2.6 g of 4-(3,4,5-trimethoxyphenyl)piperazine are mixed in 20 ml of dimethylsulfoxide, then stirred at 80°-90° C. for 5 hours. The reaction mixture is poured into 80 ml of 2% aqueous solution of sodium hydrogencarbonate and the organic layer is extracted with chloroform. The chloroform layer is washed with water, dried and chloroform is removed by distillation. The residue thus obtained is dissolved in 30 ml of ethanol and dried hydrogen chloride gas is blown into the ethanol solution. The crystals thus precipitated are collected by filtration and recrystallized from methanol-ethanol to obtain 3.2 g (yield: 61%) of 7-{3-[4-(3,4,5-trimethoxyphenyl)-piperazinyl]propoxy}-3,4-dihydrocarbostyril dihydrochloride in the form of colorless needle-like crystals with a melting point of 225°-227° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04824840
Quelldatensatzuspto-grants-1989_04
ORD IDord-6c25e9bb8ead4005a472cd4def0bbcbc
Quellennotizuspto-grants-1989_04