Réaction #45852

Équation de réaction

hydrochloric acid

trimethylaluminium

N-ethylmethylamine

ethyl 4-cyano-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-2-carboxylate

→

compound

Rendement 87.2%

4-Cyano-N-ethyl-7-fluoro-N,5-dimethyl-6-phenyl-1,3-benzoxazole-2-carboxamide

Rendement 87.2%

Solvants

dichloromethane

dichloromethane

Conditions de réaction

Traitement

1. 1
   workup.STIRRINGby stirring for 19 hours
2. 2
   workup.ADDITIONwas added to the reaction liquid
3. 3
   Températurewith cooling with ice
4. 4
   workup.STIRRINGby stirring at room temperature
5. 5
   Autrethe reaction liquid
6. 6
   Extractionwas extracted with chloroform
7. 7
   SéchageNext, the combined organic layer was dried over anhydrous magnesium sulfate
8. 8
   Filtrationfiltered
9. 9
   Concentrationthe filtrate was concentrated under reduced pressure
10. 10
    AutreThe resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane

Mode opératoire

Under nitrogen atmosphere, trimethylaluminium (1.03 M n-hexane solution) (2.40 ml, 2.47 mmol) was dropwise added at room temperature to a dichloromethane (8 ml) solution of N-ethylmethylamine (146 mg, 2.47 mmol), followed by stirring for 80 minutes. Subsequently, a dichloromethane (4 ml) solution of ethyl 4-cyano-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-2-carboxylate (I-111) (400 mg, 1.23 mmol) was dropwise added, followed by stirring for 19 hours. After the reaction, aqueous 1 N hydrochloric acid solution was added to the reaction liquid with cooling with ice, followed by stirring at room temperature, then the reaction liquid was extracted with chloroform. Next, the combined organic layer was dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=2:1, v/v) to obtain the entitled compound (362 mg, 87%) as a white solid.

Source