Reaktion #1014096

ord-6dfc1d3029a84287b08b420f140d494c

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe resulting reaction mixture
  2. 2
    WaschenThe organic layer was washed with brine
  3. 3
    Trocknendried (Na2SO4)
  4. 4
    Einengenconcentrated under reduced pressure
  5. 5
    SonstigePurification by silica gel cinematography (95% CH2Cl2, 5% MeOH)

Vorschrift

The HCl salt of (E)-methyl 4-(2-aminoethylamino)-4-oxobut-2-enoate (0.515 mmol) was taken up in 10 mL of CH3CN along with R-lipoic acid (TCI, 106 mg, 0.515 mmol), HATU (215 mg, 0.567 mmol) and DIEA (270 μl, 1.55 mmol). The resulting reaction mixture was stirred at room temperature for 18 h and diluted with EtOAc. The organic layer was washed with brine, dried (Na2SO4) and concentrated under reduced pressure. Purification by silica gel cinematography (95% CH2Cl2, 5% MeOH) afforded 120 mg of (R,E)-methyl 4-(2-(5-(1,2-dithiolan-3-yl)pentanamido)ethylamino)-4-oxobut-2-enoate. MS (EI) calcd for C15H24N2O4S: 360.12; found 361 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09289503B2uspto-grants-2016_03