Réaction #684950

ord-a3f2ef2235d34a34a297f4e40f54e2a9

Équation de réaction

CCCCc1ccc(C(=O)c2nccc3ccccc23)cc1
compound
CCCCc1ccc(C(=O)c2nccc3ccccc23)cc1
(4-Butylphenyl)(1-isoquinolyl)ketone
NN.O
hydrazine monohydrate
[K+].[OH-]
potassium hydroxide
CCCCc1ccc(Cc2nccc3ccccc23)cc1
title compound
Rendement 55.3%
CCCCc1ccc(Cc2nccc3ccccc23)cc1
1-(4-Butylbenzyl)Isoquinoline
Rendement 55.3%

Conditions de réaction

Température
160°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.WAITat 200° C. for 1 hour
  2. 2
    TempératureThe mixture was cooled to room temperature
  3. 3
    Extractionthis was extracted with ethyl acetate
  4. 4
    LavageThe extract was washed with water
  5. 5
    Séchagedried over anhydrous magnesium sulfate
  6. 6
    Concentrationconcentrated under reduced pressure
  7. 7
    AutreThe residue was purified by silica gel column chromatography

Mode opératoire

The compound of Example B3 (1.7 g, 6.0 mmol), hydrazine monohydrate (836 mg, 17 mmol), and potassium hydroxide (769 mg, 14 mmol) were added to diethylene glycol (8.5 ml), and this mixture was stirred at 80° C. for 1 hour, at 160° C. for 3.5 hours, then at 200° C. for 1 hour. The mixture was cooled to room temperature, ice water was added, and this was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (914 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07897387B2uspto-grants-2011_03