Реакция #45740

ord-2a61c6f12b354501a8bb69fbf7daa579

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe solvent was evaporated away under reduced pressure
  2. 2
    workup.ADDITIONDiethyl ether was added to the residue
  3. 3
    Концентрированиеthis was concentrated under reduced pressure

Методика

The above-obtained 2-cyclopropyl-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-6-formyl-5-methyl-1,3-benzoxazole-4-carbonitrile (50 mg, 0.15 mmol) was dissolved in ethanol (0.5 ml) and diethyl ether (1 ml), then at room temperature, 1 mol hydrochloric acid/ethanol solution (162 μl, 0.16 mmol) was added. After stirring under nitrogen atmosphere at the same temperature for 3 hours, the solvent was evaporated away under reduced pressure. Diethyl ether was added to the residue, and this was concentrated under reduced pressure. This operation was repeated further twice.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07737166B2uspto-grants-2010_06