Реакция #70513

ord-97ec8250b6ce4c9e9eb79df6beba4bf8

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwas heated
  2. 2
    Температураat reflux for 4.5 hours
  3. 3
    ДругоеThe layers were separated
  4. 4
    Экстракцияthe aqueous layer extracted with dichloromethane (2×100 ml)
  5. 5
    ПромывкаThe combined organic layers were washed with 5% aqueous citric acid (w/v, 100 ml) and brine (100 ml)
  6. 6
    Сушкаthen dried over magnesium sulphate
  7. 7
    ДругоеSolvent was removed in vacuo

Методика

A mixture of 6-bromo-4-nitro-1H-indazole (10.0 g, 0.041 mol), 3,4-dihydropyran (8.52 ml, 0.09 mol) and pyridinium para-toluene sulfonate (125 mg, 0.50 mol) in dichloromethane (150 ml) was heated at reflux for 4.5 hours. The reaction was allowed to cool to room temperature and was poured onto saturated aqueous sodium bicarbonate (200 ml). The layers were separated and the aqueous layer extracted with dichloromethane (2×100 ml). The combined organic layers were washed with 5% aqueous citric acid (w/v, 100 ml) and brine (100 ml) then dried over magnesium sulphate. Solvent was removed in vacuo to give the title compound which was used in subsequent reactions without further purification (12.89 g).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08536169B2uspto-grants-2013_09