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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392378Generated: October 27, 2026

Potassium Carbonate → N-pyrimidinyl piperidine sulfonamide

https://huagongshe.com/reaction/392378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChloropyrimidineHCID 74404—
Reactant1-PiperidinesulfonamideHCID 276741—
ReactantAmmonium formateHCID 2723923—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductN-pyrimidinyl piperidine sulfonamideHCID 2205266268%

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 (6.21 g, 13.8 mmol) was dissolved in dry dimethylformamide (28 mL) and potassium carbonate (5.7 g, 41.4 mmol) and 2-chloropyrimidine (3.16 g, 27.6 mmol) were added. The reaction was stirred at eighty five degrees Celsius for one 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 (4.94 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800646B1
Source datasetuspto-grants-2004_10
ORD IDord-5df86d4fe8ef4b8b871554e8aaa5b568
Source noteuspto-grants-2004_10