Reacción #684947

ord-63e429487d474d50b8f9c5f09af3289a

Ecuación de reacción

CCCCc1ccc(CCl)cc1
4-n-butylbenzylchloride
CN(C)C=O
dimethylformamide
[H-].[Na+]
sodium hydride
CN(C)C=O
dimethylformamide
N#CC1c2ccccc2C=CN1C(=O)c1ccccc1
1-cyano-2-benzoyl-1,2-dihydroisoquinoline
CCCCc1ccc(Cc2nccc3ccccc23)cc1
aforementioned compound
Rendimiento 17.2%
CCCCc1ccc(Cc2nccc3ccccc23)cc1
1-(4-butylbenzyl)isoquinoline
Rendimiento 17.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthis was concentrated
  2. 2
    workup.ADDITIONtoluene and water were added to this residue
  3. 3
    LavadoThe toluene layer was washed with water
  4. 4
    Secadodried over potassium carbonate
  5. 5
    Concentraciónconcentrated
  6. 6
    workup.ADDITIONTo an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added
  7. 7
    Temperaturathis was refluxed for 2 hours
  8. 8
    ConcentraciónAfter concentration, toluene and water
  9. 9
    workup.ADDITIONwere added
  10. 10
    LavadoThe toluene layer was washed with water
  11. 11
    Secadodried over calcium carbonate
  12. 12
    Concentraciónconcentrated
  13. 13
    OtroThe residue was purified by silica gel column chromatography

Procedimiento

To a dimethylformamide (1.8 ml) solution of 60% sodium hydride (16 mg, 0.40 mmol), a dimethylformamide (3.6 ml) solution of 1-cyano-2-benzoyl-1,2-dihydroisoquinoline (100 mg, 0.38 mmol) synthesized according to the literature of Org. Synth., VI, 115 (1988), and 4-n-butylbenzylchloride (70 mg, 0.38 mmol) was added dropwise under nitrogen atmosphere at −16° C., and was further stirred at room temperature for 30 minutes. Water was added, this was concentrated, and toluene and water were added to this residue. The toluene layer was washed with water, dried over potassium carbonate, and concentrated. To an ethanol (1.6 ml) solution of the residue, 50% aqueous sodium hydroxide solution (0.63 ml) was added, and this was refluxed for 2 hours. After concentration, toluene and water were added. The toluene layer was washed with water, then dried over calcium carbonate, and then concentrated. The residue was purified by silica gel column chromatography to give 18 mg of the aforementioned compound of the formula (Ia).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07897387B2uspto-grants-2011_03