Реакция #4401

ord-ff349a1b204b4c2aab891a575c293bf5

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe mixture was heated at 85°-100° C. for 1.5 hours
  2. 2
    ТемператураAfter being cooled
  3. 3
    Фильтрацияthe resulting precipitate was collected by filtration
  4. 4
    workup.DISSOLUTIONdissolved in methylene chloride
  5. 5
    workup.ADDITIONThe solution was treated successively with silica gel (4.5 g) and activated charcoal
  6. 6
    Другоеevaporated in vacuo
  7. 7
    ДругоеThe crystalline residue was recrystallized from a mixture of ethyl acetate and petroleum ether

Методика

To a solution of sodium hydride (63.6% in mineral oil dispersion, 0.285 g) in 2-propynyl alcohol (12 ml) was added 8-(2-methylbenzyloxy)-3-trimethylammoniomethyl-2-methylimidazo[1,2-a]pyridine iodide (3 g) and the mixture was heated at 85°-100° C. for 1.5 hours. After being cooled, the mixture was poured into ice-water and the resulting precipitate was collected by filtration and dissolved in methylene chloride. The solution was treated successively with silica gel (4.5 g) and activated charcoal and evaporated in vacuo. The crystalline residue was recrystallized from a mixture of ethyl acetate and petroleum ether to give 8-(2-methylbenzyloxy)-3-(2-propynyloxymethyl)-2-methylimidazo[1,2-a]pyridine (1.18 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725601uspto-grants-1988_02