Reaktion #1014085

ord-d9f6d49a180b47b1b362ef229b6c33e1

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reselling reaction mixture
  2. 2
    WaschenThe organic layer was washed with saturated aqueous NaHCO3, brine
  3. 3
    Trocknendried (Na2SO4)
  4. 4
    Einengenconcentrated under reduced pressure
  5. 5
    SonstigePurification by chromatography (95% CH2Cl2, 5% MeOH)

Vorschrift

The HCl salt of (E)-methyl 4-(2-aminoethylamino)-4-oxobut-2-enoate (8.1 mmol) was takes up in 40 mL of CH3CN along with (4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenoic acid (DHA, 2.60 g, 8.1 mmol), HATU (3.4 g, 12.1 mmol) and DIEA (4.2 mL). The reselling reaction mixture was stirred at room temperature for 2 h and diluted with EtOAc. The organic layer was washed with saturated aqueous NaHCO3, brine, dried (Na2SO4) and concentrated under reduced pressure. Purification by chromatography (95% CH2Cl2, 5% MeOH) afforded 1.4 g of (E)-methyl 4-(2-(4Z,7Z,10Z,13Z,16Z,19Z)-docosa-4,7,10,13,16,19-hexaenamidoethylamino)-4-oxobut-2-enoate. MS (EI) calcd for C29H42N2O4: 482.31; found 483 (M+1).

Quelle

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