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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649235Generated: October 26, 2026

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

https://huagongshe.com/reaction/1649235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVesnarinoneHCID 5663—
ReactantDimethylformamideHCID 6228—
ReactantBenzyl ChlorideHCID 7503—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
Product1-Benzyl-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-3,4-dihydrocarbostyril hemihydrateHCID 88739270—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415572
Source datasetuspto-grants-1983_11
ORD IDord-9f8f5f37da7c44aab41dab4ec74ca058
Source noteuspto-grants-1983_11