Реакция #64129

ord-8ac1f04fc7bf4b3182f969b016355951

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ЭкстракцияIt is extracted with dichloromethane
  2. 2
    Сушкаthe organic phases are dried with sodium sulfate
  3. 3
    workup.DISTILLATIONthe solvent is distilled off
  4. 4
    ДругоеThe residue is chromatographed on silica gel with dichloromethane/methanol
  5. 5
    Другое406 mg (45% of theory) is isolated

Методика

838 mg of 3-(2-bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea (2 mmol) is dissolved in 100 ml of dichloromethane, 1.2 g of anhydrous aluminum chloride (9 mmol) and 1.8 ml of dichloromethyl methyl ether (20 mmol) are added and stirred for 15 minutes at room temperature. The reaction mixture is mixed with ice and, after 15 minutes, with a solution of 1.5 g of tartaric acid in 50 ml of water and made alkaline with 5 ml of conc. ammonia solution. It is extracted with dichloromethane, the organic phases are dried with sodium sulfate and the solvent is distilled off. The residue is chromatographed on silica gel with dichloromethane/methanol, 406 mg (45% of theory) is isolated.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05411966uspto-grants-1995_05