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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927600Generated: October 25, 2026

Potassium Carbonate → N-(1-{4-[3-(3,5-Dimethyl-isoxazol-4-yl)-ureido]-2-fluoro-phenyl}-piperidin-4-yl)-2-ethyl-N-phenyl-butyramide

https://huagongshe.com/reaction/1927600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
Reactant2-ethyl-N-phenyl-N-piperidin-4-yl-butyramideHCID 69303647—
ReactantN-[1-(4-amino-2-fluoro-phenyl)-piperidin-4-yl]-2-ethyl-N-phenyl-butyramideHCID 69305096—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-(1-{4-[3-(3,5-Dimethyl-isoxazol-4-yl)-ureido]-2-fluoro-phenyl}-piperidin-4-yl)-2-ethyl-N-phenyl-butyramideHCID 16667231—

Reaction Conditions

Temperature50 °C

Reaction Steps

N-[1-(4-amino-2-fluoro-phenyl)-piperidin-4-yl]-2-ethyl-N-phenyl-butyramide. To a mixture of 2-ethyl-N-phenyl-N-piperidin-4-yl-butyramide (10 mmol) and K2CO3 (40 mmol) in DMF (30 mL) was added 1,2-difluoro-4-nitro-benzene (1.6 g, 10 mmol). The reaction mixture was stirred at 50° C. for 3 h, then was diluted with H2O (500 mL). The solution was decanted, leaving a semi-solid, which was collected and re-dissolved into 1:1 EtOH/EtOAc (100 mL). The mixture was treated with SnCl2.2H2O (10 g) and was heated at 100° C. for 16 h. The mixture was cooled to rt, diluted with ice water (100 mL), basified to pH=9 with NaHCO3, and extracted with EtOAc (3×200 mL). The organic layers were combined, dried (Na2SO4), and concentrated to give the crude title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183239B2
Source datasetuspto-grants-2012_05
ORD IDord-77606713bf5a461b827f2d1fdbd4d815
Source noteuspto-grants-2012_05