Reaktion #1443

ord-58cd2e04d7a34df7b31f8a8ce82f18d5

Reaktionsgleichung

Cc1ccc(-c2ccccc2C(=O)Nc2ccc(C(=O)N3CCc4nc(C)[nH]c4-c4ccccc43)cc2)cc1
2-(4-Methylphenyl)-4'-[(2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepin-6-yl)carbonyl]benzanilide
CCOC(C)=O.Cl
hydrochloric acid ethyl acetate
Cc1ccc(-c2ccccc2C(=O)Nc2ccc(C(=O)N3CCc4nc(C)[nH]c4-c4ccccc43)cc2)cc1.Cl
2-(4-methylphenyl)-4'-[(2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepin-6-yl)carbonyl]benzanilide hydrochloride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled on an ice bath
  2. 2
    Filtrationthe thus precipitated crystals were collected by filtration
  3. 3
    Waschenwashed with a small volume of ethyl alcohol

Vorschrift

2-(4-Methylphenyl)-4'-[(2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepin-6-yl)carbonyl]benzanilide was dissolved in 10 ml of ethyl alcohol, the resulting solution was mixed with 0.37 ml of 4N hydrochloric acid-ethyl acetate and cooled on an ice bath and then the thus precipitated crystals were collected by filtration and washed with a small volume of ethyl alcohol to obtain 500 mg of 2-(4-methylphenyl)-4'-[(2-methyl-1,4,5,6-tetrahydroimidazo[4,5-d][1]benzazepin-6-yl)carbonyl]benzanilide hydrochloride (Example 19(2)).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723606uspto-grants-1998_03