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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1649235Erstellt: 26. Oktober 2026

Vesnarinone → 1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate

https://huagongshe.com/reaction/1649235

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVesnarinoneHCID 5663—
EduktDimethylformamideHCID 6228—
EduktBenzyl ChlorideHCID 7503—
EduktSodium hydrideHCID 24758—
LösungsmittelWaterHCID 962—
Produkt1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrateHCID 88739270—

Reaktionsschritte

6-[4-(3,4-Dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril (500 mg) and 70 mg of 60% oily sodium hydride were mixed with 5 ml of DMF and stirred at room temperature for 1 hour. Then, to the mixture was added dropwise 3 ml of DMF solution containing 0.17 ml of benzylchloride. After stirring for 4 hours at room temperature, the reaction mixture was poured into a large amount of water and organic substances were extracted with chloroform. The chloroform layer was washed with water and dehydrated. Chloroform was distilled off and the residue was recrystallized from ethanol to give 150 mg of 1-benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrate, m.p. 131.5°-132.5° C., yellow powders. Elemental Analysis for

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04415572
Quelldatensatzuspto-grants-1983_11
ORD IDord-9f8f5f37da7c44aab41dab4ec74ca058
Quellennotizuspto-grants-1983_11