Реакция #54722

ord-3fb33d54a1214c609a58ae0ecba1218f

Уравнение реакции

Nc1cc(N2CC=CCC2)nc(N)[n+]1[O-]
2,4-diamino-6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxide
ClCCl
methylene chloride
CCCCCCCCOC(=O)Cl
chloroformic acid octyl ester
CCCCCCCCOC(=O)Nc1cc(N2CC=CCC2)nc(NC(=O)OCCCCCCCC)[n+]1[O-]
dioctyl 6-[3,6-dihydro-1(2H)-pyridyl]-2,4-pyrimidine-dicarbamate-3-oxide

Растворители

Условия реакции

Температура
5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture is cooled for 30 minutes
  2. 2
    workup.STIRRINGstirred at room temperature for 1 hour
  3. 3
    ЭкстракцияThe mixture is extracted with methylene chloride
  4. 4
    Промывкаwashed with water
  5. 5
    Сушкаdried over magnesium sulfate
  6. 6
    Другоеevaporated under reduced pressure
  7. 7
    ДругоеThe residue is recrystallized from methylene chloride/ethanol, there

Методика

10 G. of 2,4-diamino-6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxide are suspended in 150 ml. of methylene chloride and 20 ml. of triethylamine. The suspension is cooled to 5° C. and 28 g. of chloroformic acid octyl ester are added dropwise while stirring. The mixture is cooled for 30 minutes and then stirred at room temperature for 1 hour. The mixture is extracted with methylene chloride, washed with water, dried over magnesium sulfate and evaporated under reduced pressure. The residue is recrystallized from methylene chloride/ethanol, there being obtained dioctyl 6-[3,6-dihydro-1(2H)-pyridyl]-2,4-pyrimidine-dicarbamate-3-oxide, having a melting point of 64° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04150132uspto-grants-1979_04