Reacción #2192102

ord-708f03ab94ee494fbde9369227d65195

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónAfter concentration
  2. 2
    Otroa rotary evaporator and oil pump vacuum at 40° C.
  3. 3
    Otrothe residue is purified by preparative HPLC
  4. 4
    OtroThe product is obtained as an oil

Procedimiento

170 mg of 1-(4-fluorophenyl)-3-[3-(4-fluorophenyl)-3-hydroxypropyl]-4-[4-(5-iodopentyloxy)phenyl]azetidin-2-one are dissolved in 5 ml of absolute dimethylformamide. 220 mg of 6-methylaminohexane-1,2,3,4,5-pentaol are then added, and the reaction solution is stirred at 50° C. for 2 h. After concentration using a rotary evaporator and oil pump vacuum at 40° C., the residue is purified by preparative HPLC. The product is obtained as an oil. C36H46F2N2O8 (672) MS (ESI): M+

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07576200B2uspto-grants-2009_08