Réaction #5136

ord-f1b3d2d807af4226b0d71e242805c55b

Équation de réaction

COC(=O)c1ccc2c(c1)C(NC(=O)CCl)c1ccccc1CO2
methyl 11-chloroacetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
c1c[nH]cn1
imidazole
COC(=O)c1ccc2c(c1)C(NC(=O)Cn1ccnc1)c1ccccc1CO2
product
COC(=O)c1ccc2c(c1)C(NC(=O)Cn1ccnc1)c1ccccc1CO2
Methyl 11-(1-imidazolyl)acetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureto cool
  2. 2
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  3. 3
    ExtractionThe obtained residue was extracted with 300 ml of methylene chloride
  4. 4
    LavageThe extract was washed successively with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution
  5. 5
    SéchageAfter drying over anhydrous sodium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  7. 7
    LavageThe resulting residue was subjected to silica gel column chromatography (eluting solvent; chlororform:methanol=10:1)

Mode opératoire

Crude methyl 11-chloroacetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate, 3.0 g, was heated to reflux for 4 hours in 100 ml of toluene together with 0.9 g of imidazole. After allowing to cool, the solvent was distilled off under reduced pressure. The obtained residue was extracted with 300 ml of methylene chloride. The extract was washed successively with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluting solvent; chlororform:methanol=10:1) to give 1.6 g of the product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05242931uspto-grants-1993_09