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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279246Generated: November 1, 2026

Potassium Carbonate → N-pyrimidinyl piperidine sulfonamide

https://huagongshe.com/reaction/1279246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-PiperidinesulfonamideHCID 276741—
ReactantAmmonium formateHCID 2723923—
Reactant2-Chloro-5-ethylpyrimidineHCID 3572763—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductN-pyrimidinyl piperidine sulfonamideHCID 2205266260%

Reaction Steps

To a slurry of the piperidine sulfonamide from part F (6.3 g, 12.0 mmol) in methanol (25 mL) was added ammonium formate (2.2 g, 34.5 mmol). The system was purged with nitrogen for 10 minutes. The nitrogen stream was removed and palladium on carbon (1.2 g 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 (4.5 g, 10 mmol) was dissolved in dry dimethylformamide (20 mL) and potassium carbonate (3.45 g, 325 mmol) and 2-chloro-5-ethylpyrimidine (1.82 mL, 15 mmol) were added. The reaction was stirred at eighty degrees Celsius for four hour 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-pyrimidinyl piperidine sulfonamide as a white solid (3.33 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448250B1
Source datasetuspto-grants-2002_09
ORD IDord-1d6eb77857504c2897462f9ce39aa333
Source noteuspto-grants-2002_09