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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646738Generated: November 1, 2026

Potassium Carbonate → HCID 19786575, compound

https://huagongshe.com/reaction/1646738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 2772144—
ReactantHCID 19786560HCID 19786560—
CatalystPotassium IodideHCID 4875—
SolventDimethylformamideHCID 6228—
ProductHCID 19786575HCID 1978657546.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution consisting of 5-(3-chloropropyl)-3-(2-fluorophenyl)-6,7-dihydro-1,2-benzisoxazol-4(5H)-one (1.36 g) and DMF (40 ml) was added anhydrous potassium carbonate (0.3 g), diisopropylethyl amine (0.8 ml), 3-piperazinyl-1,2-benzisothiazol (1.26 g) and potassium iodide (27 mg) at room temperature with stirring. The flask was flushed with nitrogen and warmed to 80° C. for 12 hours. Upon cooling to room temperature, water and ethyl acetate were added to the reaction mixture. The layers were separated and the aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried (MgSO4). Filtration and concentration gave the crude product. Purification via flash column chromatography (silica gel, 20% triethylamine/ether) afforded 1.0 g of 5-[3-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]propyl]-3-(2-fluorophenyl)-6,7-dihydro-1,2-benzisoxazol-4(5H)-one as a foam. The product was flushed through alumina with dichloromethane. The hydrochloride was prepared by dissolving the free amine with menthanol and adding ethereal HCl. The salt was filtered and washed with pentane, m.p. 215° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180834
Source datasetuspto-grants-1993_01
ORD IDord-c0c49a603daa49e4b0c2cd3fcea692d3
Source noteuspto-grants-1993_01