تفاعل #2015405
ord-8e2c796f13a841b1bfcb61041646e3ab
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةTo a cooled
- 2أخرىThe mixture was evaporated to dryness and saturated NaHCO3 solution (5 mL), diethyl ether and heptane
- 3workup.ADDITIONwere added
- 4workup.STIRRINGThe mixture was stirred at room temperature for 1 h
- 5ترشيحthe precipitate was collected by filtration
- 6أخرىfurther 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.