تفاعل #2015426

ord-ebfa819229d945a2b940ef7132fffa9e

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe catalyst was removed by filtration
  2. 2
    أخرىthe obtained solution evaporated
  3. 3
    أخرىThe crude product was further purified by crystallization from diethyl ether/hexane

الإجراء التجريبي

To a stirred suspension of 2-(3′-nitro-biphenyl-3-yl)-4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyrimidine (1.6 g, 3.27 mmol) in MeOH (40 mL) was added at room temperature Pd—C (10%, 0.16 g) and THF (40 mL). The mixture was stirred at room temperature under H2 atmosphere for 2 h, the catalyst was removed by filtration and the obtained solution evaporated. The crude product was further purified by crystallization from diethyl ether/hexane to yield the title compound as an off-white solid (1.28 g, 85%). MS (ISP) 460.2 [(M+H)+]; mp 156.5° C.

المصدر

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