Reacción #1006002

Ecuación de reacción

Me3Al

ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate

(4-(trifluoromethoxy)phenyl)methanamine

→

6-bromo-N-(4-(trifluoromethoxy)-benzyl)imidazo[1,2-a]pyridine-2-carboxamide

Disolventes

methylene chloride

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGThe reaction mixture was stirred at 50° C. for 20 hours
2. 2
   TemperaturaAfter cooling to room temperature
3. 3
   Otrothe reaction was quenched by 1N HCl solution (2-3 mL)
4. 4
   OtroThe reaction mixture was partitioned between methylene chloride and water
5. 5
   ExtracciónThe aqueous layer was extracted with methylene chloride
6. 6
   LavadoThe combined organic layer was washed with brine
7. 7
   Secadodried over anhydrous magnesium sulfate
8. 8
   ConcentraciónAfter concentration
9. 9
   Otrothe residue was purified by flash chromatography (ethyl acetate:hexane=1:1)

Procedimiento

Me3Al (2.0M solution in toluene) (2.78 ml, 5.57 mmol) was added to a solution of ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate (500 mg, 1.85 mmol) in methylene chloride (10 ml) at 0° C. The reaction mixture was stirred at room temperature for 2 hours. (4-(trifluoromethoxy)phenyl)methanamine (0.42 ml, 2.78 mmol) was added to the above mixture at room temperature. The reaction mixture was stirred at 50° C. for 20 hours. After cooling to room temperature, the reaction was quenched by 1N HCl solution (2-3 mL). The reaction mixture was partitioned between methylene chloride and water. The aqueous layer was extracted with methylene chloride. The combined organic layer was washed with brine, then dried over anhydrous magnesium sulfate. After concentration, the residue was purified by flash chromatography (ethyl acetate:hexane=1:1) to give the title compound, 6-bromo-N-(4-(trifluoromethoxy)-benzyl)imidazo[1,2-a]pyridine-2-carboxamide, as a solid (440 mg, 57% yield).

Fuente