تفاعل #616569

ord-0a49b87eefda4021a22eb9616a1cb162

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe mixture was concentrated
  2. 2
    workup.ADDITIONthe residue was treated with saturated NaHCO3 solution
  3. 3
    استخلاصextracted with DCM (3×)
  4. 4
    تجفيفThe extract was dried (Na2SO4)
  5. 5
    تركيزconcentrated
  6. 6
    أخرىThe residue was dried under vacuum

الإجراء التجريبي

To a solution of (R)-tert-butyl 3-((2,2,2-trifluoro-N-((1R,2S)-2-phenylcyclopropyl)acetamido)methyl)pyrrolidine-1-carboxylate (1.28 g, 3.10 mmol) in dichloromethane (DCM) (12 mL) was added TFA (3 ml, 38.9 mmol), and the mixture was stirred at room temperature for 3 h. The mixture was concentrated and the residue was treated with saturated NaHCO3 solution and extracted with DCM (3×). The extract was dried (Na2SO4) and concentrated. The residue was dried under vacuum to give 950 mg of product as pale yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09346840B2uspto-grants-2016_05