Reaktion #532169

ord-3952a3c47a4d442bba89141f86fddeb0

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was almost dry
  2. 2
    workup.ADDITIONEtOAc was added
  3. 3
    Sonstigethe precipitate was removed by filtration
  4. 4
    ExtraktionThe filtrate was extracted with 0.1 N HCl (2×), brine (1×)
  5. 5
    Trocknendried (Na2SO4)
  6. 6
    Einengenconcentrated

Vorschrift

5-(15-tert-Butoxycarbonyl-pentadecanoylamino)-isophthalic acid mono-tert-butyl ester (140 mg, 0.25 mmol) was dissolved in dry THF (3.5 ml). TSTU (95 mg, 0.30 mmol) and DIPEA (70 ul, 0.30 mmol) were added. The mixture was stirred at RT under nitrogen over the week-end. The reaction mixture was almost dry. EtOAc was added and the precipitate was removed by filtration. The filtrate was extracted with 0.1 N HCl (2×), brine (1×), dried (Na2SO4) and concentrated to give the title compound as a syrup containing a trace of an impurity in a quantitative yield (0.165 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08476228B2uspto-grants-2013_07