تفاعل #44130

ord-cf90e6509db44c63a078279acad2d9c7

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux under nitrogen for 3 hours
  2. 2
    أخرىquenched
  3. 3
    استخلاصextracted with ethyl acetate (3×20 mL)
  4. 4
    تجفيفdried over sodium sulfate
  5. 5
    تركيزconcentrated under reduced pressure
  6. 6
    أخرىThe crude was purified by flash chromatography on silica gel
  7. 7
    غسيلeluting with dichloromethane-methanol (95:5)

الإجراء التجريبي

(2R)-2-Methylpiperazine (0.550 g; 2 eq), caesium carbonate (1.78 g; 2 eq), palladium acetate (0.123 g; 0.2 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.513 g; 0.3 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) (0.8 g; 1 eq) in toluene (30 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 3 hours. The reaction cooled to room temperature, quenched using saturated aqueous ammonium chloride solution (15 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel, eluting with dichloromethane-methanol (95:5) affording the title compound in 58% yield (0.383 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07732600B2uspto-grants-2010_06