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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383458Generated: October 30, 2026

Sodium Iodide → HCID 21187763, compound

https://huagongshe.com/reaction/1383458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 70245335HCID 70245335—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 21187763HCID 21187763—

Reaction Steps

The mixture of benzhydryl-piperidin-4-yl-amine hydrogen bromide salt (1.74 g, 5 mmol, 1.0 eq.), N-(2-bromoethyl)phthalimide (1.27 g, 5 mmol, 1.0 eq.), K2CO3 (1.73 g, 12.5 mmol, 2.5 eq.), and NaI (1.05 g, 7.0 mmol, 1.4 eq.) in 2-butanone (20 ml) was refluxed for 2-3 hours. The mixture was then cooled to room temperature. The white solid was filtered off and was washed with small amount of CHCl3. The filtrates were combined and concentrated. The resulted residue was dissolved in CHCl3 (100 ml). The solution was washed with water (3×20 ml), then dried over anhydrous Na2SO4. After removed all solvent, the crude product 2-{2-[4-(benzhydryl-amino)-piperidin-1-yl]-ethyl} -isoindole-1,3-dione was yielded (2.70 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255323B1
Source datasetuspto-grants-2001_07
ORD IDord-024c91153859407cad07ff94336b5eeb
Source noteuspto-grants-2001_07