Réaction #486948

ord-98847f26054a4698b46b52d5555dfa9f

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreat 45° C
  2. 2
    Extractionthe reaction mixture was extracted with chloroform (10×5 mL)
  3. 3
    SéchageThe combined organic extracts were dried over anhydrous sodium sulfate
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated
  6. 6
    AutreThe residue obtained
  7. 7
    Autrewas chromatographed on a silica gel column
  8. 8
    workup.ADDITIONwith a chloroform: methanol mixture containing 1% triethylamine as eluent

Mode opératoire

An aqueous methylamine solution (5 mL, 40%, 58.7 mmole) was mixed with XII (200 mg, 0.08 mmole) and stirred for 3 hr. in a sealed tube at 45° C. After the reaction was complete, water (10 mL) was added to the cooled reaction mixture, and the reaction mixture was extracted with chloroform (10×5 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated. The residue obtained was chromatographed on a silica gel column using methanol:chloroform (1:9) and then with a chloroform: methanol mixture containing 1% triethylamine as eluent. About 70 mg of XIII was obtained as a slightly yellow syrup, which was distilled at 110°-112° C., 0.04 mm Hg. XIII was converted to its mono fumarate salt form, which exhibits a melting point of 103°-104° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05824692uspto-grants-1998_10