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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262548Generated: October 25, 2026

Potassium Iodide → 1-[4-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-butyl]-4,4-dimethyl-piperidine-2,6-dione

https://huagongshe.com/reaction/1262548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(1-Piperazinyl)-1,2-benzisothiazoleHCID 2772144—
Reactant1-(4-Bromobutyl)-4,4-dimethylpiperidine-2,6-dioneHCID 13660335—
SolventAcetonitrileHCID 6342—
Product1-[4-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-butyl]-4,4-dimethyl-piperidine-2,6-dioneHCID 1323249364%

Reaction Steps

A mixture of N-(4-bromobutyl)-3,3-dimethylglutarimide (4 g., 0.0145 mole) obtained according to the procedure of Example 9, 3-(1-piperazinyl)-1,2-benzisothiazole (3.18 g., 0.0145 mole), anhydrous potassium carbonate (20.04 g., 0.145 mole) and potassium iodide (0.25 g., 0.0015 mole) in 150 ml. of acetonitrile is stirred and refluxed for a period of 12 hr. The reaction mixture is filtered, concentrated in vacuo and residual material triturated with ether. Crystallization of the solid thus obtained from ether affords a 64% yield of analytically pure 1-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]-4,4-dimethyl-2,6-piperidinedione, m.p. 146°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04452799
Source datasetuspto-grants-1984_06
ORD IDord-4ee7ab1d3b7b470290fa374199e17d71
Source noteuspto-grants-1984_06