Réaction #1994260

ord-a96a6ae6207e48c5a850b724648051a9

Équation de réaction

c1ccc(-c2ccc(N3c4ccccc4Cc4cc(-c5ccccc5)ccc43)cc2)cc1
10-(biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine
O=C1CC(Br)C(=O)N1
bromosuccinimide
Brc1ccc2c(c1)Cc1cc(-c3ccccc3)ccc1N2c1ccc(-c2ccccc2)cc1
10-(biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine
Rendement 70.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagethe resultant solution was washed with distilled water
  2. 2
    ExtractionThen, an organic layer was extracted
  3. 3
    Séchagedried with sodium sulfate so as
  4. 4
    Autreto remove the solvent
  5. 5
    AutreThe residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/10))

Mode opératoire

10-(biphenyl-4-yl)-2-phenyl-9,10-dihydroacridine (7.8 g, 19.0 mmol) was added with chloroform (300 ml), and with bromosuccinimide (3.7 g, 21.0 mmol). The resultant solution was stirred at room temperature for 2 hours. After the reaction was completed, the resultant solution was washed with distilled water. Then, an organic layer was extracted and dried with sodium sulfate so as to remove the solvent. The residue was purified by silica gel column chromatography (methylene chloride/n-hexane (1/10)) to obtain 10-(biphenyl-4-yl)-2-bromo-7-phenyl-9,10-dihydroacridine compound (pale yellow solid, 6.5 g, yield 70%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08597802B2uspto-grants-2013_12