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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477176Generated: October 26, 2026

Dimethylformamide → 6-[4-(2-Phenyl-2-hydroxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochloride

https://huagongshe.com/reaction/477176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant(3-Chlorophenyl)(piperazin-1-yl)methanoneHCID 1074765—
Reactant6-(2-Chloroacetyl)-1,2,3,4-tetrahydroquinolin-2-oneHCID 4961790—
SolventWaterHCID 962—
Product6-[4-(2-Phenyl-2-hydroxyethyl)-1-piperazinylcarbonyl]-3,4-dihydrocarbostyril monohydrochlorideHCID 131716209—

Reaction Conditions

Temperature55 °C

Reaction Steps

To 60 ml of anhydrous dimethylformamide solution containing 6.7 g of 6-(α-chloroacetyl)-3,4-dihydrocarbostyril was added 11.5 g of 4-(3-chlorobenzoyl)piperazine and 5 ml of triethylamine and the whole mixture was stirred at 50 to 60° C. for 1 hour. The reaction mixture was poured into a large amount of water, and the organic layer was extracted with chloroform. The chloroform layer was washed with water, dried, then chloroform was removed by evaporation. The residue thus obtained was recrystallized from methanol-chloroform to yield 5.5 g of 6-[-4-(3-chlorobenzoyl)-1-piperazinylacetyl]-3,4-dihydrocarbostyril 1/2-hydrate in the form of colorless powdery substance. Melting point: 231°-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886809
Source datasetuspto-grants-1989_12
ORD IDord-9a6a6ea73ee74987b7d27f19eae57234
Source noteuspto-grants-1989_12