Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483444Generated: November 2, 2026

Sodium Iodide → HCID 21744304, compound

https://huagongshe.com/reaction/483444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Fluorophenyl)(piperidin-1-yl)methanoneHCID 2737266—
ReactantHCID 19752303HCID 19752303—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 21744304HCID 217443049.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of N-methyl-N-(3-chloropropyl)-1,2-benzisothiazole-3-carboxamide (7.13 g), 1-(4-fluorobenzoyl)piperidine (6.44 g), potassium carbonate (7.33 g), and sodium iodide (300 mg) in dry 1-methyl-2-pyrrolidinone (150 ml) was heated to 120° C., with stirring, under nitrogen. After 24 hrs, the mixture was allowed to cool to room temperature, and the residue was partitioned between ethyl acetate/water. The organic phase was washed with water, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The crude residue was chromatographed twice on silica using 10:90 methanol:ethyl acetate as the eluent. The appropriate fractions were collected and evaporated. The residue was dissolved in ether and hydrogen chloride in ethanol was added. Recrystallized of the precipitate from dichloromethane/ether gave 0.642 g (5.09%) of product, mp 189°-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225412
Source datasetuspto-grants-1993_07
ORD IDord-cf2750056e904efd8a8552f159bcfc1c
Source noteuspto-grants-1993_07