Реакция #4435

ord-3616968c1a0f4c4397905a7c8fdd4da3

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with chloroform
  2. 2
    ПромывкаThe organic layer was washed with brine
  3. 3
    Сушкаdried over sodium sulfate
  4. 4
    Другоеevaporated
  5. 5
    ДругоеThe residue was chromatographed on silica gel eluting with chloroform

Методика

To a solution of 6-(3,4-dimethoxyphenyl)-3-methyl-1,2,3,4-tetrahydro-4-(2,4,6-trimethylphenylimino)pyrimidine (0.5 g) in pyridine (5 ml) was added acetic anhydride (1.0 ml), and the mixture was stirred at ambient temperature for 2.5 hours. The mixture was poured into water (150 ml) and extracted with chloroform. The organic layer was washed with brine, dried over sodium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with chloroform to give 1-acetyl-6-(3,4-dimethoxyphenyl)-3-methyl-1,2,3,4-tetrahydro-4-(2,4,6-trimethylphenylimino)pyrimidine (0.22 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725600uspto-grants-1988_02