Реакция #49810

ord-6d6ed009073d40378300b3f99b4e6525

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеsubsequently concentrated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in ethyl acetate
  3. 3
    Промывкаwashed three times with water
  4. 4
    Сушкаdried (sodium sulfate)
  5. 5
    Концентрированиеconcentrated

Методика

The compound of Example 2 (988 mg, 5.0 mmol) was dissolved in 30 ml of anhydrous pyridine. After addition of 0.6 ml (5.5 mmol) of isopropenyl chloroformate, the mixture was stirred at room temperature for 4 h and subsequently concentrated. The residue was dissolved in ethyl acetate and washed three times with water, dried (sodium sulfate) and concentrated. After chromatography on silica gel (ethyl acetate/heptane=1:2), the desired compound was isolated and crystallized from diethyl ether/pentane; yield 380 mg (27%) of melting point 86°-87° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05424311uspto-grants-1995_06