Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460675Generated: November 2, 2026

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

https://huagongshe.com/reaction/1460675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1-(3-Chlorobenzoyl)piperazineHCID 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° C.-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05071856
Source datasetuspto-grants-1991_12
ORD IDord-c4ac326aebd54108b464e99ad6876787
Source noteuspto-grants-1991_12