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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929735Generated: October 27, 2026

Potassium Iodide → 2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-[1-(2-methylthiazol-4-ylmethyl)piperidin-4-yl]acetamide

https://huagongshe.com/reaction/929735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloromethyl)-2-methyl-1,3-thiazole--hydrogen chloride (1/1)HCID 2734203—
Reactant2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-(piperidin-4-yl)acetamideHCID 9946526—
SolventAcetonitrileHCID 6342—
Product2-(4-Methoxyphenyl)-N-(4-methylbenzyl)-N-[1-(2-methylthiazol-4-ylmethyl)piperidin-4-yl]acetamideHCID 68952697—

Reaction Conditions

Temperature82 °C

Reaction Steps

50ELH87 (0.3 g, 0.852 mmol, 1.0 eq) and 4-(chloromethyl)-2-methylthiazole hydrochloride (0.235 g, 1.5 eq) were added to a 7 ml vial and dissolved in acetonitrile (3 ml). Potassium carbonate (141.3 g, 1.2 eq) and a crystal of potassium iodide were added and the vial was sealed and shaken for 20 h at 82° C. The reaction mixture was extracted with distilled water (made basic by potassium carbonate, pH 10) and dichloromethane. The crude product was dried with sodium sulfate and concentrated. After purification by HPLC the product was converted into the hydrochloride salt by dissolving the free base in 1 ml dichloromethane and adding 1 eq. HCl in ether (2M). This mixture was added drop-wise to an excess of heptane where the product precipitated. The solvent was removed by evaporation leaving a white powder as the product. yield 83.8 mg (21%), UV/MS 100/90 (M+ 463), rt (B, MS) 11.82.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296694B2
Source datasetuspto-grants-2016_03
ORD IDord-9059f99f9ad349e98a4bfbba22d68c5b
Source noteuspto-grants-2016_03