Реакция #60565

ord-edf55ea1959844a7beb69242da746a76

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAfter concentration
  2. 2
    Другоеby evaporation in a vacuum
  3. 3
    Экстракцияextracted with 40 ml of methylene chloride
  4. 4
    ПромывкаThe methylene chloride phase is washed with water
  5. 5
    Другоеdried
  6. 6
    Фильтрацияfiltered
  7. 7
    Концентрированиеconcentrated by evaporation
  8. 8
    Другоеpurified on silica gel

Методика

200 mg (0.75 mmol) of 4-amino-N-(2-diethylamino-ethyl)-2-methoxy-benzamide in 10 ml of chloroform is mixed with 5 ml of 3,4-methylenedioxybenzoic acid chloride (in chloroform) and this mixture is stirred for 3 hours at room temperature. After concentration by evaporation in a vacuum, the residue is taken up in 40 ml of dilute sodium bicarbonate solution and then extracted with 40 ml of methylene chloride. The methylene chloride phase is washed with water, dried, filtered and concentrated by evaporation. The crude product, 315 mg, is taken up in methylene chloride and purified on silica gel. As a mobile solvent, a mixture that consists of methylene chloride/methanol (97:3→90:10) is used. 210 mg (67% of theory) of benzo[1,3]dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbamoyl)-5-methoxy-phenyl]-amide (melting point 131.1° C.) is obtained.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07427390B2uspto-grants-2008_09