Reacción #2487456

Ecuación de reacción

potassium carbonate

N-(2-bromo-5-chloro-4-methoxyphenyl)-2,2,2-trifluoroacetamide

phenylacetylene

triethylamine

→

title compound

6-Chloro-5-methoxy-2-phenyl-1H-indole

Disolventes

acetonitrile

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.WAITThe reaction mixture was left
2. 2
   Temperaturato cool
3. 3
   workup.STIRRINGThe mixture was stirred at 120° C. for 2 more hours under microwave irradiation
4. 4
   workup.WAITThe reaction mixture was left
5. 5
   Temperaturato cool
6. 6
   Filtraciónfiltered through Celite (registered trademark)
7. 7
   ConcentraciónThe filtrate was concentrated under reduced pressure
8. 8
   OtroThe residue was purified by aminopropylated silica gel column chromatography (eluting solvent: ethyl acetate-hexane)

Procedimiento

To a mixture of N-(2-bromo-5-chloro-4-methoxyphenyl)-2,2,2-trifluoroacetamide (512 mg), phenylacetylene (0.254 mL), copper(I) iodide (17.5 mg), triethylamine (0.549 mL), and acetonitrile (12.3 mL) was added bis(triphenylphosphine) palladium(II) dichloride (32.5 mg). The mixture was stirred at 120° C. for 2 hours under microwave irradiation. The reaction mixture was left to cool. To the reaction mixture was added potassium carbonate (532 mg). The mixture was stirred at 120° C. for 2 more hours under microwave irradiation. The reaction mixture was left to cool, and filtered through Celite (registered trademark). The filtrate was concentrated under reduced pressure. The residue was purified by aminopropylated silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (255 mg). 1H-NMR (CDCl3) δ ppm: 3.95 (3H, s), 6.70-6.80 (1H, m), 7.13 (1H, s), 7.30-7.50 (4H, m), 7.60-7.70 (2H, m), 8.00-8.40 (1H, br).

Fuente