Reacción #470391

ord-b99acdb60f3f4cef8075d2903a148c0e

Ecuación de reacción

c1ccc(-c2nc3ccccc3[nH]2)cc1
2-phenyl-1H-benzo[d]imidazole
CCO
ethanol
CC(C)c1ccccc1-n1c(-c2ccccc2)nc2ccccc21
desired product
CC(C)c1ccccc1-n1c(-c2ccccc2)nc2ccccc21
1-(2-isopropylphenyl)-2-phenyl-1H-benzo[d]imidazole

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was heated up
  2. 2
    Temperaturato reflux for 24 hours
  3. 3
    Filtraciónthe precipitate was collected by filtration
  4. 4
    OtroThe product was purified by column chromatography

Procedimiento

Intermediate 1 (1.5 g, 2.1 mmol) and 142-isopropylphenyl)-2-phenyl-1H-benzo[d]imidazole (2 g, 6.4 mmol) were mixed with 30 ml of ethanol in a three-neck flask under nitrogen. The mixture was heated up to reflux for 24 hours. After cooled to room temperature, the precipitate was collected by filtration. The product was purified by column chromatography using 1:2 dichloromethane and hexanes as eluent. 0.7 g of desired product was obtained after purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08367223B2uspto-grants-2013_02