Реакция #1958050

ord-f7df5b9b129b43b3b7b30f16aba072ea

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe resulting solution was concentrated to dryness
  2. 2
    Другоеthe title compound precipitated as powder
  3. 3
    Другоеwas isolated by filtration

Методика

The title compound was prepared from 8-methyl-3-(4-methylphenyl)-8-azabicyclo[3.2.1]octan-3-ol (3.4 g, 14.7 mmol), glacial acetic acid (11 mL) and concentrated hydrochloric acid (11 mL). The free base of the title compound was dissolved in diethyl ether and added fumaric acid (1.3 g, 11.2 mmol) in methanol. The resulting solution was concentrated to dryness, the residue was trituated in diethyl ether, the title compound precipitated as powder and was isolated by filtration. Yield 2.46 g (51%) m.p. 156.8-157.4° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06100275uspto-grants-2000_08