Réaction #1857589
ord-07afc07c0aec4f2f827fd5473d6d55ab
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1AutreThe solvent and the excess reagent were removed under reduced pressure
- 2workup.DISSOLUTIONThe solid residue was again dissolved in dichloromethane (5 ml) and, at 0° C.
- 3workup.STIRRINGThe reaction mixture was stirred at room temperature overnight
- 4Autrethe aqueous phase was removed
- 5Extractionextracted with ethyl acetate
- 6SéchageThe combined organic phases were dried over sodium sulphate
- 7Concentrationconcentrated
- 8AutrePurification by column chromatography
Mode opératoire
To a solution of [3,5-bis-(difluoromethyl)-1H-pyrazol-1-yl]acetic acid (58 mg) in dichloromethane (20 ml) were added, at 0° C., oxalyl chloride (94.5 mg) and one drop of N,N-dimethylformamide. The reaction mixture was stirred at room temperature for 2 hours. The solvent and the excess reagent were removed under reduced pressure. The solid residue was again dissolved in dichloromethane (5 ml) and, at 0° C., added dropwise to a solution of 4-{4-[5-(2-fluoro-6-formylphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidinium chloride and triethylamine (5.0 eq.) in dichloromethane (15 ml). The reaction mixture was stirred at room temperature overnight. Then it was admixed with concentrated sodium hydrogencarbonate solution, and the aqueous phase was removed and extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate and concentrated. Purification by column chromatography gave 2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-fluorobenzaldehyde (55 mg).