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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279245Generated: October 26, 2026

Potassium Carbonate → N-pyrimidinyl piperidine sulfonamide

https://huagongshe.com/reaction/1279245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-PiperidinesulfonamideHCID 276741—
ReactantAmmonium formateHCID 2723923—
Reactant2-Chloro-4-(trifluoromethyl)pyrimidineHCID 2773912—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductN-pyrimidinyl piperidine sulfonamideHCID 2205266276%

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 (4.14 g, 30 mmol) and 2-chloro-4-trifluoromethylpyrimidine (2.4 mL, 20 mmol) were added. The reaction was stirred at seventy degrees Celsius for three 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 (4.51 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448250B1
Source datasetuspto-grants-2002_09
ORD IDord-26d548ec1220462998fda6a9de57c34b
Source noteuspto-grants-2002_09