Reaktion #2857

ord-91ec8de0a1e542cc9e6a284639bbfc6c

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe solution is concentrated
  2. 2
    workup.DISSOLUTIONThe residue is dissolved in CH2 Cl2
  3. 3
    WaschenThe resulting solution is washed with water and saturated NaCl
  4. 4
    TrocknenThe organic layer is dried over MgSO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe crude product is purified by column chromatography
  8. 8
    Wascheneluting with a gradient of 40% CH2Cl2 /hexanes to 60% CH2Cl2 /hexanes

Vorschrift

5H-Thieno[3,2-c]pyridin-4-one (1.0 g, 6.62 mmol) is dissolved in 30 mL of phosphorous oxy chloride. The solution is heated to 100° C. After 4 h, the solution is concentrated. The residue is dissolved in CH2 Cl2. The resulting solution is washed with water and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with a gradient of 40% CH2Cl2 /hexanes to 60% CH2Cl2 /hexanes. The title compound (1.0 g, 5.8 mmol) is obtained as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731315uspto-grants-1998_03