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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358498Generated: October 29, 2026

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

https://huagongshe.com/reaction/358498

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 numberUS04468402
Source datasetuspto-grants-1984_08
ORD IDord-2ffd4ec607d641519f3b7bf60999cdc7
Source noteuspto-grants-1984_08