Реакция #48275

ord-42fb344170e94a92985abc60d64e31f2

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияAfter completion of the reduction the reaction mixture is filtered through hyflo
  2. 2
    workup.ADDITIONthe filtrate diluted with water
  3. 3
    Экстракцияthe water/methanol mixture then extracted with ethyl acetate
  4. 4
    ПромывкаThe combined ethyl acetate extracts are washed with saturated aqueous sodium chloride solution
  5. 5
    Сушкаdried over magnesium sulphate
  6. 6
    Концентрированиеconcentrated in vacuo

Методика

A solution of 194 g of 6-(Chloro-difluoro-methyl)-2-(3-methoxy-propyl)-nicotinic acid methyl ester (prepared according to WO 04/078729) in methanol (ca. 2 liter) and triethylamine (100 ml) is hydrogenated at 1 Atm hydrogen pressure in the presence of 2 g of 5% palladium supported on carbon. After completion of the reduction the reaction mixture is filtered through hyflo, and the filtrate diluted with water and the water/methanol mixture then extracted with ethyl acetate. The combined ethyl acetate extracts are washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate and then concentrated in vacuo to give 194.2 g 6-Difluoromethyl-2-(3-methoxy-propyl)-nicotinic acid methyl ester as a pale coloured oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745495B2uspto-grants-2010_06