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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074247Generated: October 31, 2026

Sodium Iodide → Tert-butyl 4-[3-(4-isoquinolin-1-ylpiperazin-1-yl)propyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/2074247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantCesium carbonateHCID 10796—
ReactantTert-butyl 4-(3-((methylsulfonyl)oxy)propyl)piperidine-1-carboxylateHCID 21190098—
Reactant1-Piperazin-1-yl-isoquinoline dihydrochlorideHCID 57421832—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 4-[3-(4-isoquinolin-1-ylpiperazin-1-yl)propyl]piperidine-1-carboxylateHCID 5750776478.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

A DMI (20 ml) suspension of tert-butyl 4-{3-[(methylsulfonyl)oxy]propyl}piperidine-1-carboxylate (1.00 g), 1-piperazin-1-yl-isoquinoline dihydrochloride (980 mg), cesium carbonate (1.02 g) and sodium iodide (467 mg) was stirred at 140° C. for 1 hour. EtOAc was added to the reaction liquid, washed with water and aqueous saturated sodium hydrogencarbonate solution in that order, then dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=1:1 (v/v)) to obtain tert-butyl 4-[3-(4-isoquinolin-1-ylpiperazin-1-yl)propyl]piperidine-1-carboxylate (1.07 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919494B2
Source datasetuspto-grants-2011_04
ORD IDord-6d3ef7fe3b064cad99adade445a0065d
Source noteuspto-grants-2011_04