Reacción #2464348

ord-e430ef1aee064c7fbbe2880c3b9c0a0e

Ecuación de reacción

CCOC(C)=O
ethyl acetate
OC1CN(CCCOCCc2ccc3sccc3c2)C1
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol
O.O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid monohydrate
CCOC(C)=O
ethyl acetate
O=C(O)CC(O)(CC(=O)O)C(=O)O.OC1CN(CCCOCCc2ccc3sccc3c2)C1
1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol citrate
Rendimiento 89.8%

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONby adding
  2. 2
    workup.DISSOLUTIONdissolution
  3. 3
    TemperaturaThe reaction mixture was heated at 40° C.
  4. 4
    workup.STIRRINGthe resulting mixture was stirred at 40° C. for 10 minutes
  5. 5
    OtroThe crystals precipitated
  6. 6
    Filtraciónwere collected by filtration

Procedimiento

In 14.4 mL of ethanol was dissolved 10.0 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol, followed by adding thereto 7.21 g of citric acid monohydrate, and the resulting mixture was heated at 50° C. to effect dissolution. To the resulting solution were added 35 mL of ethyl acetate and 5.6 mL of ethanol at 50° C., and stirred at 25° C. The reaction mixture was heated at 40° C., after which ethyl acetate (45 mL) was added dropwise thereto and the resulting mixture was stirred at 40° C. for 10 minutes and then at 10 to 20° C. for 1 hour. The crystals precipitated were collected by filtration to obtain 14.9 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-azetidinol citrate as colorless crystals.

Fuente

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