Reaktion #7534

ord-5c37f61942b04b9e986f75c9bbc72dab

Reaktionsgleichung

Cl
hydrochloric acid
ClCCCOCCc1ccc2ccsc2c1
6-[2-(3-chloropropoxy)ethyl]-1-benzothiophene
Cl.OC1CNC1
3-azetidinol hydrochloride
O=C([O-])[O-].[K+].[K+]
potassium carbonate
OC1CN(CCCOCCc2ccc3ccsc3c2)C1
1-{3-[2-(1-benzothiophen-6-yl)ethoxy]propyl}-3-azetidinol
Ausbeute 24.5%

Reaktionsbedingungen

Temperatur
75°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwere added to the solution
  2. 2
    workup.WAITat 95° C. for 1.5 hours
  3. 3
    TemperaturAfter the reaction mixture was cooled
  4. 4
    Sonstigethe aqueous layer was separated
  5. 5
    workup.ADDITIONEthyl acetate was added to the aqueous layer
  6. 6
    Sonstigeafter which the organic layer was separated
  7. 7
    WaschenThe organic layer was washed with water
  8. 8
    Trocknena saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  9. 9
    workup.DISTILLATIONdistilled under reduced pressure
  10. 10
    Sonstigeto remove the solvent
  11. 11
    SonstigeThe residue was purified by a column chromatography (eluent; chloroform:methanol=30:1 to 5:1)

Vorschrift

In 5 mL of dimethyl sulfoxide was dissolved 1.00 g of 6-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 0.86 g of 3-azetidinol hydrochloride and 1.63 g of potassium carbonate were added to the solution. The resulting mixture was stirred at 75° C. for 2.5 hours and then at 95° C. for 1.5 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the pH was adjusted to 1 with 6 mol/L hydrochloric acid, and the aqueous layer was separated. Ethyl acetate was added to the aqueous layer and the. pH was adjusted to 10 with a 2 mol/L aqueous sodium hydroxide solution, after which the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=30:1 to 5:1) to obtain 0.28 g of 1-{3-[2-(1-benzothiophen-6-yl)ethoxy]propyl}-3-azetidinol as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087594B2uspto-grants-2006_08