Реакция #1135793

ord-1acb623c566f4e2c97459275d7b8c2a3

Уравнение реакции

CI
methyl iodide
Cc1c(F)cccc1-n1nn[nH]c1=O
1-(2-methyl-3-fluorophenyl)-1,4-dihydrotetrazole-5-one
CN(C)C=O
N,N-dimethylformamide
[H-].[Na+]
sodium hydride
Cc1c(F)cccc1-n1nnn(C)c1=O
1-(2-methyl-3-fluorophenyl)-4-methyl-1,4-dihydrotetrazole-5-one

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураcooling
  2. 2
    ДругоеTo the reaction mixtures
  3. 3
    Температураcooling
  4. 4
    ТемператураThe mixtures were raised to room temperature
  5. 5
    workup.STIRRINGwere stirred for fourteen hours
  6. 6
    ДругоеTo the reaction mixtures
  7. 7
    Экстракцияthe mixtures were extracted with ethyl acetate
  8. 8
    ПромывкаThe organic layers were washed with 10% hydrochloric acid, water and saturated saline
  9. 9
    Сушкаwere dried over anhydrous magnesium sulfate
  10. 10
    Концентрированиеwere then concentrated under reduced pressure

Методика

To a mixture of the above-mentioned 1-(2-methyl-3-fluorophenyl)-1,4-dihydrotetrazole-5-one 10.00 g and N,N-dimethylformamide 100 mL was added 55% sodium hydride 2.47 g under ice-cooling. The mixtures were raised to room temperature and were stirred for one hour. To the reaction mixtures was added methyl iodide 3.5 mL under ice-cooling. The mixtures were raised to room temperature and were stirred for fourteen hours. To the reaction mixtures was added water and the mixtures were extracted with ethyl acetate. The organic layers were washed with 10% hydrochloric acid, water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure. The resulting residues were subjected to a silica gel column chromatography to give 1-(2-methyl-3-fluorophenyl)-4-methyl-1,4-dihydrotetrazole-5-one 2.19 g.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09380782B2uspto-grants-2016_07