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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886158Generated: October 31, 2026

Sodium Iodide → HCID 15294872, compound

https://huagongshe.com/reaction/1886158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPotassium CarbonateHCID 11430—
Reactant94427-39-1HCID 612990—
ReactantHCID 14441092HCID 14441092—
Reactant4-(3,4-Dimethoxyphenyl)piperidin-4-olHCID 15034714—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 15294872HCID 1529487233.4%

Reaction Steps

To a solution of 3.76 g of 4-(3,4-dimethoxyphenyl)-1,2,5,6-tetrahydropyridine (V-7), which was prepared by the reaction of 4-hydroxy-4-(3,4-dimethoxyphenyl)piperidine and p-toluenesulfonic acid, and 2.94 g of 1-(3-chloropropylcarbamoyl)-2-oxopyrrolidine in 35 ml of DMF is added 3.98 g of K2CO3 and 3.22 g of NaI. The reaction mixture is stirred at 100°-105° C. for 6 days under nitrogen gas. After cooling to room temperature, the mixture is diluted with ethyl acetate, washed with brine and dried over MgSO4. After removal of the solvent, the residue is subjected to column chromatography with silica gel, eluting with CH2Cl2 /MeOH (20/1) to prepare 1.78 g (Yield: 33.4%) of the compound (Ia-105) as solid. The oxalate is recrystallized from iPrOH-MeOH to prepare needles. mp. 178.0°-182.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149817
Source datasetuspto-grants-1992_09
ORD IDord-b9c0d989fc104250a0e3dbb9bcc0241c
Source noteuspto-grants-1992_09