تفاعل #50137

ord-add641abc96540deb9dda91baff95149

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISTILLATIONThe solvent is distilled off
  2. 2
    workup.ADDITIONto the resulting residue is added chloroform
  3. 3
    غسيلthe mixture is washed
  4. 4
    أخرىdried
  5. 5
    أخرىevaporated
  6. 6
    أخرىto remove the solvent
  7. 7
    أخرىThe residue is purified by silica gel column chromatography (solvent; chloroform/ethanol=10:1)

الإجراء التجريبي

To a mixture of the compound obtained in Example 12 (1.70 g) and pyridine (20 ml) is added acetic anhydride (5 ml), and the mixture is stirred overnight. The solvent is distilled off, and to the resulting residue is added chloroform, and the mixture is washed, dried, and evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent; chloroform/ethanol=10:1) to give methyl 2-n-butyl-5-acetyl-3-(2'-methoxycarbonylbiphenyl-4-yl)methyl-4,5,6,7-tetrahydroimidazo[4,5-c] pyridine-4-carboxylate (0.47 g) as an oil. NMR (CDCl3) δ: 0.88 (3H, t), 2.21 (3H, s), 3.46 (3H, s), 3.64 (3H, s), 5.33 (2H, ABq)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05424316uspto-grants-1995_06