تفاعل #2015405

ord-8e2c796f13a841b1bfcb61041646e3ab

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةTo a cooled
  2. 2
    أخرىThe mixture was evaporated to dryness and saturated NaHCO3 solution (5 mL), diethyl ether and heptane
  3. 3
    workup.ADDITIONwere added
  4. 4
    workup.STIRRINGThe mixture was stirred at room temperature for 1 h
  5. 5
    ترشيحthe precipitate was collected by filtration
  6. 6
    أخرىfurther purified by flash chromatography (heptane/ethyl acetate) and crystallization (dichloromethane/MeOH)

الإجراء التجريبي

To a cooled and stirred solution of 3′-[4-(3-methyl-4-trifluoromethyl-phenyl)-6-trifluoromethyl-pyrimidin-2-yl]-biphenyl-3-sulfonic acid tert-butylamide (0.52 g) in dichloromethane (6 mL) was added TFA (6 mL) and the reaction mixture was allowed to stir at room temperature for 15 h. The mixture was evaporated to dryness and saturated NaHCO3 solution (5 mL), diethyl ether and heptane were added. The mixture was stirred at room temperature for 1 h, the precipitate was collected by filtration and further purified by flash chromatography (heptane/ethyl acetate) and crystallization (dichloromethane/MeOH) to yield the title compound as an white solid (0.29 g, 54%). MS (ISP) 536.2 [(M−H)−]; mp 205° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08183262B2uspto-grants-2012_05