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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297583Generated: October 27, 2026

Potassium Carbonate → N-methoxyethyl piperidinesulfonamide

https://huagongshe.com/reaction/2297583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
Reactant1-PiperidinesulfonamideHCID 276741—
ReactantAmmonium formateHCID 2723923—
SolventMethanolHCID 887—
ProductN-methoxyethyl piperidinesulfonamideHCID 2205257253%

Reaction Steps

To a slurry of the piperidine sulfonamide from part F (420 mg, 0.8 mmol) in methanol (15 mL) was added ammonium formate (147 mg, 2.3 mmol). The system was purged with nitrogen for 10 minutes. The nitrogen stream was removed and palladium on carbon (80 mg of 10 weight % on activated carbon, 50% water) was added. The reaction was refluxed for forty five minutes, cooled, filtered through Celite under nitrogen, and concentrated in vacuo. The residue was dissolved in dry dimethylformamide (5 mL) and potassium carbonate (150 mg, 1.07 mmol) and 2-bromoethyl methyl ether (100 uL, 1.07 mmol) were added. The reaction was stirred at thirty five degrees Celsius for thirty hours and then concentrated in vacuo. The residue was taken up in ethyl acetate and filtered through Celite. The filtrate washed with water two times, saturated sodium chloride solution, dried over Na2SO4, filtered, and concentrated in vacuo. The product was recrystallized (methanol) to give the N-methoxyethyl piperidine sulfonamide as an off-white solid (190 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492367B1
Source datasetuspto-grants-2002_12
ORD IDord-15e63d496ef346e3afd8ea4f480ee0e0
Source noteuspto-grants-2002_12