Reacción #2464343

ord-389ee7bdaf6846aba5e3bea6e918aee5

Ecuación de reacción

O=C(O)CCOCCc1ccc2sccc2c1
3-[2-(1-benzothiophen-5-yl)ethoxy]propionic acid
O=S(Cl)Cl
thionyl chloride
OC1CN(CCCOCCc2ccc3sccc3c2)C1
3-hydroxyazetidine
OC1CN(CCCOCCc2ccc3sccc3c2)C1
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol
[Na+].[OH-]
sodium hydroxide
O=C(CCOCCc1ccc2sccc2c1)N1CC(O)C1
3-[2-(1-benzothiophen-5-yl)ethoxy]-1-(3-hydroxy-1-azetidinyl)-1-propanone
Rendimiento 117.8%

Condiciones de reacción

Temperatura
15°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.STIRRINGstirred at room temperature for 1 hour
  3. 3
    Otrothe organic layer was separated
  4. 4
    LavadoThe organic layer was washed with diluted hydrochloric acid
  5. 5
    Secadoa saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONdistilled under reduced pressure
  7. 7
    Otroto remove the solvent
  8. 8
    OtroThe residue was purified by a column chromatography (eluent; chloroform:acetone=3:1 to 1:1)
  9. 9
    Otrocrystallized from diisopropyl ether

Procedimiento

In 12.5 mL of toluene was suspended 5.00 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]propionic acid, and 0.1 mL of N,N-dimethylformamide was added thereto, after which 1.68 mL of thionyl chloride was added dropwise thereto at 15° C. and the resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was added dropwise to a solution of 4.44 g of 3-hydroxyazetidine 1/2 tartrate and 3.76 g of sodium hydroxide in 25 mL of water at 10° C., and stirred at room temperature for 1 hour. Ethyl acetate was added to the reaction mixture and the organic layer was separated. The organic layer was washed with diluted hydrochloric acid 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:acetone=3:1 to 1:1) and crystallized from diisopropyl ether to obtain 5.48 g of 3-[2-(1-benzothiophen-5-yl)ethoxy]-1-(3-hydroxy-1-azetidinyl)-1-propanone as colorless crystals.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07468443B2uspto-grants-2008_12