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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434588Generated: November 2, 2026

Potassium Iodide → 1,1-Dimethylethyl 4-(4-{[3-(2-methyl-1-piperidinyl)propyl]oxy}phenyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1434588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-MethylpiperidineHCID 7974—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[4-(3-Chloro-propoxy)-phenyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 58817843—
SolventWaterHCID 962—
SolventMethyl Ethyl KetoneHCID 6569—
Product1,1-Dimethylethyl 4-(4-{[3-(2-methyl-1-piperidinyl)propyl]oxy}phenyl)-1-piperazinecarboxylateHCID 5793581288.2%

Reaction Steps

1,1-Dimethylethyl 4-{4-[(3-chloropropyl)oxy]phenyl}-1-piperazinecarboxylate (D9) (1.6 g), was dissolved in 2-butanone (10 ml). Potassium carbonate (1.38 g) and a catalytic amount of potassium iodide were added, followed by 2-methylpiperidine (0.99 g). The mixture was heated at reflux for 72 h under nitrogen. The reaction mixture was diluted with water and extracted with dichloromethane. The organic phases were separated using a hydrophobic frit, combined and evaporated in vacuo. The residue was purified on a 100 g silica SPE bond elut cartridge, eluting with a gradient of 0% to 20% [0.880 ammonia-methanol (1:9)]-dichloromethane mixtures, to give the title compound (1.66 g). LCMS RT=2.48 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615550B2
Source datasetuspto-grants-2009_11
ORD IDord-fbb85dd625344279bfbf535f430b3292
Source noteuspto-grants-2009_11