Réaction #531818
ord-cc9345925d1249abb23c8341bead0fc5
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1TempératureThe reaction mixture was heated
- 2Températureat reflux for 4.5 hours
- 3AutreThin layer chromatography on silica gel confirmed completion of the reaction
- 4Filtrationfiltered through Celite®
- 5Lavageby washing three times with 10% aqueous sodium bicarbonate solution
- 6ExtractionThe organic extract
- 7Séchagewas dried (MgSO4)
- 8Concentrationconcentrated under reduced pressure
- 9Autrethe residual solid was purified by chromatography on silica gel
Mode opératoire
To a solution of 1-(3-chloro-2-pyridinyl)-N-[4-iodo-2-methyl-6-[(methylamino)carbonyl]phenyl]-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide (i.e. the diamide product of Step A) (410 mg, 0.72 mmol) in tetrahydrofuran (8 mL) was added copper(I) iodide (24 mg, 0.126 mmol), tetrakis(triphenyphosphine)palladium(0) (70 mg, 0.060 mmol) and copper(I) cyanide (640 mg, 7.2 mmol) sequentially at room temperature. The reaction mixture was heated at reflux for 4.5 hours. Thin layer chromatography on silica gel confirmed completion of the reaction. The reaction mixture was then diluted with ethyl acetate (20 mL) and filtered through Celite®, followed by washing three times with 10% aqueous sodium bicarbonate solution and once with brine. The organic extract was dried (MgSO4) and concentrated under reduced pressure and the residual solid was purified by chromatography on silica gel to afford 114 mg of the title compound, a compound of the present invention, as a white solid, melting at 214-216° C.