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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262851Generated: November 3, 2026

Sodium Chloride → 6-(4-Benzyl-1-piperazinylcarbonyl)-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1262851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Oxo-1,2,3,4-tetrahydroquinoline-6-carboxylic acidHCID 7131909—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Product6-(4-Benzyl-1-piperazinylcarbonyl)-3,4-dihydrocarbostyrilHCID 1319533537.2%

Reaction Steps

To a solution of 50 ml of dimethylformamide with 5.0 g of 6-carboxy-3,4-dihydrocarbostyril and 4 ml of triethylamine, 3.87 g of isobutyl chloroformate in 2 ml of dimethylformamide solution was added dropwise. After stirring at a room temperature for 30 minutes, 5.5 g of benzylpiperazine in 3 ml of dimethylformamide solution was added to the former solution and stirred at a room temperature for 30 minutes, then stirred continuously at 50°-60° C. for 1 hour. The reaction mixture was poured into a voluminous amount of a saturated sodium chloride aqueous solution and extracted with chloroform and the chloroform extract was washed with water and dried. After removal of the solvent, to the residue thus obtained was added diethyl ether to crystallize the residue and recrystallized from ethanol to obtain 3.4 g of 6-(4-benzyl-1-piperazinylcarbonyl)-3,4-dihydrocarbostyril. Colorless needle-like crystals. Melting point: 198°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04454130
Source datasetuspto-grants-1984_06
ORD IDord-0a881a9924034524accfaf4fc1b5fb4c
Source noteuspto-grants-1984_06