Reaktion #60565

ord-edf55ea1959844a7beb69242da746a76

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenAfter concentration
  2. 2
    Sonstigeby evaporation in a vacuum
  3. 3
    Extraktionextracted with 40 ml of methylene chloride
  4. 4
    WaschenThe methylene chloride phase is washed with water
  5. 5
    Sonstigedried
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated by evaporation
  8. 8
    Sonstigepurified on silica gel

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07427390B2uspto-grants-2008_09