Reaktion #86507

ord-9fe9c0f779b44f3eb27919e12ed66e9c

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted twice with 1 N HCl
  2. 2
    Extraktionextracted with methylene chloride
  3. 3
    WaschenThe combined organic layers were washed with brine
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    Einengenconcentrated under reduced pressure

Vorschrift

To a stirred solution of 2-(1-azidopropyl)-3-iodo-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (3.10 g, 8.40 mmol) in tetrahydrofuran (20 mL) and water (6.06 mL) was added a 1.0 M solution of trimethylphosphine in tetrahydrofuran (0.1 mmol) at room temperature and stirred for 1 hour. To the mixture was added EtOAc and the mixture was extracted twice with 1 N HCl. The combined extracts were neutralized with solid sodium bicarbonate and extracted with methylene chloride. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was used directly in next step (2.58 g, 89.5%). LCMS calculated for C12H15IN3O (M+H)+: m/z=344.0. Found: 344.2.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434746B2uspto-grants-2016_09