Reacción #90296

ord-bf696df99e3c42e4bef874a61be84a2e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe solvents were evaporated to dryness
  2. 2
    Otrothe crude solid was triturated with diethyl ether (15 mL)
  3. 3
    Filtraciónfiltered
  4. 4
    Otrodried

Procedimiento

A mixture of 1-(3,4-bis(benzyloxy)-5-nitrophenyl)-2-(2-(trifluoromethyl)pyridin-3-yl)ethanone (0.485 g, 0.93 mmol), ethyl carbazate (0.11 g, 1.06 mmol) and p-toluene sulfonic acid (4 mg) in toluene (10 mL) was refluxed until distillation of water ceased. The reaction mixture was cooled to room temperature, the solvents were evaporated to dryness, and the crude solid was triturated with diethyl ether (15 mL), filtered and dried yielding (Z)-ethyl 2-(1-(3,4-bis(benzyloxy)-5-nitrophenyl)-2-(2-(trifluoromethyl)pyridin-3-yl)ethylidene)-hydrazinecarboxylate, 0.475 g (84%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09446012B2uspto-grants-2016_09