Реакция #61817

ord-166f3619cbcf47aaa0bfe35595d71ac8

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGstirred
  2. 2
    workup.WAITover night
  3. 3
    Экстракцияthe mixture was extracted with ethyl acetate tree times
  4. 4
    СушкаThe combined organic phases were dried (sodium sulphate)
  5. 5
    Другоеevaporated

Методика

A solution of 97 mg (0.42 mmol) 3-methyl-4-(4-[1,2,3]triazol-1-yl-butyl)phenol in 4.0 ml N,N-dimethylformamide was treated at 0° C. with 17 mg (0.42 mmol) of 60% sodium hydride and stirred at 0° C. for 30 min. Then 100 mg (0.42 mmol) 2-Chloromethyl-6-(3-chloro-phenyl)-pyridine were added and stirred continued at r. t. over night. After addition of 8 ml water, the mixture was extracted with ethyl acetate tree times. The combined organic phases were dried (sodium sulphate) and evaporated. Chromatography on silica (eluent: ethyl acetate/n-heptane 2:1) gave 0.151 g (83%) the title compound as white powder.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07429605B2uspto-grants-2008_09