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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248402Generated: October 25, 2026

Potassium Iodide → 3-{1-(Cyclopropylmethyl)-4-piperidinyl}-1,2-benzisothiazole hydrobromide

https://huagongshe.com/reaction/1248402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant(Chloromethyl)cyclopropaneHCID 80013—
Reactant4-(3-Benzisothiazolyl) piperidineHCID 13324093—
ReactantEther hydrobromideHCID 86739792—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product3-{1-(Cyclopropylmethyl)-4-piperidinyl}-1,2-benzisothiazole hydrobromideHCID 2025575425%

Reaction Steps

A stirred mixture of 5.0 g of 3-(4-piperidinyl)-1,2-benzisothiazole, 2.30 g of cyclopropylmethyl chloride, 7.95 g of potassium carbonate, 0.25 g of potassium iodide and 90 ml of dimethylformamide was heated at 90° for 20 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The organic extract was dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and saturated hydrogen bromide/ether solution was added dropwise to precipitate the salt. The salt was recrystallized two times from ethyl acetate/ethanol to yield 2.0 g (25%) of product, mp 214°-216°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04524074
Source datasetuspto-grants-1985_06
ORD IDord-0d7b6b4ab3ef469f896c583ccb057d7a
Source noteuspto-grants-1985_06