Реакция #2816

ord-09f79ec740dc49de8727d8657531ecd2

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеat 45° C
  2. 2
    Экстракцияthe reaction mixture was extracted with chloroform (10×5 mL)
  3. 3
    СушкаThe combined organic extracts were dried over anhydrous sodium sulfate
  4. 4
    Фильтрацияfiltered
  5. 5
    Концентрированиеconcentrated
  6. 6
    ДругоеThe residue obtained
  7. 7
    Другоеwas chromatographed on a silica gel column
  8. 8
    workup.ADDITIONwith a chloroform: methanol mixture containing 1% triethylamine as eluent

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05731314uspto-grants-1998_03