Reaktion #644906

Reaktionsgleichung

4-{4-[(2-Phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester

→

2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (4-piperidin-4-yl-phenyl)-amide

Ausbeute 92.7%

Lösungsmittel

methylene chloride

trifluoroacetic acid

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe solvents were evaporated
2. 2
   SonstigeThe residue was partitioned between methylene chloride and dilute sodium hydroxide solution
3. 3
   WaschenThe organic layer was washed with brine
4. 4
   Trocknendried over sodium sulfate
5. 5
   SonstigeEvaporation of solvents

Vorschrift

4-{4-[(2-Phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-piperidine-1-carboxylic acid tert-butyl ester (245 mg, 0.475 mmol) from above was dissolved in methylene chloride (2 mL) and trifluoroacetic acid (1 mL). The mixture was stirred at room temperature and the solvents were evaporated. The residue was partitioned between methylene chloride and dilute sodium hydroxide solution. The organic layer was washed with brine and dried over sodium sulfate. Evaporation of solvents gave 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (4-piperidin-4-yl-phenyl)-amide (183 mg) as a white solid. LC-MS calcd for C22H20F3N3O2 (m/e) 415.41, obsd 416.0. The NMR spectrum obtained on the sample is compatible with its structure.

Quelle