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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119385Generated: November 1, 2026

Sodium Iodide → HCID 53742785, compound

https://huagongshe.com/reaction/2119385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl (3R,5S)-3,5-dimethylpiperazine-1-carboxylateHCID 10822535—
SolventAcetonitrileHCID 6342—
ProductAmmoniaHCID 222—
ProductHCID 53742785HCID 5374278540.5%

Reaction Steps

Potassium carbonate (1.79 g) was added to a solution of tertbutyl (cis)-3,5-dimethyl-1-piperazinecarboxylate (2.57 g) [see Preparation 5] in acetonitrile (10 ml). The reaction mixture was stirred at room temperature for 5 minutes, after which time N(2-bromoethyl) phthalimide (3.36 g) was added and the mixture was stirred for a further 4 hours. Sodium iodide (0.1 g) was added and the reaction mixture was heated to reflux for 18 hours. The mixture was then cooled and the solvent removed under reduced pressure. The residue was partitioned between ethyl acetate and water, the organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 4:1:0, changing to 0:95:5, by volume, hexane:ethyl acetate:0.88 aqueous ammonia solution, to afford tert-butyl (cis)-4-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-3,5-dimethyl-1-piperazinecarboxylate (0.94 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686357B1
Source datasetuspto-grants-2004_02
ORD IDord-4630047cdaa94655b4dda4d018ebf4fd
Source noteuspto-grants-2004_02