Reaktion #51177

Reaktionsgleichung

methyl (3-formylphenyl)-5-oxopyrrolidine-3-carboxylate

2-aminopyridine

AcOH

→

methyl 5-oxo-1-{3-((2-pyridylamino)methyl)phenyl}pyrrolidine-3-carboxylate

Lösungsmittel

trimethylorthoformate

Reaktionsbedingungen

Aufarbeitung

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

Vorschrift

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.

Quelle