تفاعل #51177

ord-e2bc81ed5ea54e5ab82e0fb636dba177

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزThe reaction mixture was concentrated in vacuo
  2. 2
    workup.DISSOLUTIONthe residue was re-dissolved in methanol
  3. 3
    workup.ADDITIONAcOH was added
  4. 4
    تركيزThe reaction solution was then concentrated in vacuo
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in EtOAc
  6. 6
    غسيلorganic solution was washed with saturated NaHCO3 twice
  7. 7
    تجفيفThe organic layer was dried over Na2SO4
  8. 8
    تركيزconcentrated in vacuo
  9. 9
    أخرىThe crude product was purified by silica gel chromatograph (10% meOH/EtOAc)
  10. 10
    أخرىto provide an orange oil

الإجراء التجريبي

A solution of methyl (3-formylphenyl)-5-oxopyrrolidine-3-carboxylate, 2-aminopyridine, and AcOH in trimethylorthoformate was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo and the residue was re-dissolved in methanol. The solution was then cooled to 0° C. AcOH was added followed by NaBH3CN solid in portions. The reaction was allowed to stirred at room temperature for 8 hours. The reaction solution was then concentrated in vacuo. The residue was dissolved in EtOAc and organic solution was washed with saturated NaHCO3 twice. The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude product was purified by silica gel chromatograph (10% meOH/EtOAc) to provide an orange oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849639B2uspto-grants-2005_02