Reacción #45883

Ecuación de reacción

hydrochloric acid

Methyl (4-cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl)acetate

trimethylaluminium n-hexane

dimethylamine hydrochloride

→

compound

Rendimiento 83.0%

2-(4-Cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl)-N,N-dimethylacetamide

Rendimiento 83.0%

Disolventes

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaby heating
2. 2
   Temperaturaunder reflux in an oil bath at 120° C. for 15 hours
3. 3
   workup.ADDITIONwas added to the reaction liquid
4. 4
   ExtracciónAfter extraction with ethyl acetate
5. 5
   Lavadothe obtained organic layer was washed with saturated brine
6. 6
   Secadodried over anhydrous sodium sulfate
7. 7
   Otrothe insoluble matter was separated by filtration
8. 8
   Otrothe residue obtained by concentration
9. 9
   Otrowas purified by preparative TLC (eluent, chloroform

Procedimiento

At room temperature, trimethylaluminium/n-hexane solution (1.03 mol/l) (547 μl, 0.563 mmol) was added to a toluene (2 ml) suspension of dimethylamine hydrochloride (38.3 mg, 0.469 mmol), followed by stirring at room temperature for 30 minutes. Methyl (4-cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl)acetate (I-295) (65.0 mg, 0.188 mmol) was added to the reaction liquid, followed by heating under reflux in an oil bath at 120° C. for 15 hours. With cooling with ice, 1 N hydrochloric acid was added to the reaction liquid. After extraction with ethyl acetate, the obtained organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, then the insoluble matter was separated by filtration, and the residue obtained by concentration was purified by preparative TLC (eluent, chloroform:methanol=10:1, v/v) to obtain the entitled compound (56.0 mg, 83%) as a white solid.

Fuente