Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241588Generated: October 25, 2026

Potassium Carbonate → 7-[4-(4-benzisoxazolyl-1-piperidinyl)-butoxy]-3,4-dihydro-2(1H)-quinolinone hydrochloride

https://huagongshe.com/reaction/241588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-oneHCID 10467467—
Reactant4-(3-Benzisothiazolyl) piperidineHCID 13324093—
ReactantEthanol hydrochlorideHCID 21887872—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
Product7-[4-(4-benzisoxazolyl-1-piperidinyl)-butoxy]-3,4-dihydro-2(1H)-quinolinone hydrochlorideHCID 6717875644%

Reaction Steps

7-(4-chlorobutoxy)-3,4-dihydro-2(1H)-quinolinone (297 mg, 1 mmol), 3-(4-piperidinyl)-1,2-benzisothiazole (220 mg, 1 mmol), and anhydrous potassium carbonate powder (414 mg, 3.3 mmol) are added to 10 ml and react at reflux for 24 hours. The reaction solution is evaporated to dryness and dispersed with 20 ml of dichloromethane and 20 ml of water respectively. The organic layer is extracted with water (20 ml×2) and saturated saline (20 ml) successively, dried over anhydrous magnesium sulfate, and evaporated to dryness to obtain a light yellow powder, which is dissolved into 5 ml of acetone and stirred in an ice bath to precipitate a white solid. The white solid is filtered, washed with small amount of acetone, and dried to obtain 260 mg of a whiter powder. The whiter powder is dissolved into anhydrous ethanol and thereto is drop-added HCl/EtOH to adjust to pH=2 to precipitate a white deposit, which is filtered out and recrystallized in anhydrous ethanol to obtain 200 mg of a product, with a yield of 44%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653069B2
Source datasetuspto-grants-2014_02
ORD IDord-db1f90e93f864f7693a5cfd999412ff1
Source noteuspto-grants-2014_02