Реакция #68073

ord-61fa375f994c46e0b7fe62df0eb7eb6b

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    Температураrefluxed
  3. 3
    Температураwith heating for 5 hours
  4. 4
    Другоеthe solvent was removed under reduced pressure, water
  5. 5
    workup.ADDITIONwas added
  6. 6
    ДругоеThe solvent was removed under reduced pressure
  7. 7
    Другоеthe residue thus obtained
  8. 8
    Другоеwas purified by reversed-phase silica gel column chromatography [eluent; acetonitrile:water=3:7]

Методика

To 0.8 mL of an ethanol solution containing 80 mg of ethyl 4-(3-(7-methoxy-2-oxoquinolin-1(2H)-yl)propyl)-1-(3-phenylpropyl)piperidine-4-carboxylate, 0.2 mL of 20% aqueous sodium hydroxide solution was added and refluxed with heating for 5 hours. After the reaction mixture was cooled to the room temperature, the solvent was removed under reduced pressure, water was added, and adjusted to pH 6.8 with 6.0 mol/L hydrochloric acid. The solvent was removed under reduced pressure, and the residue thus obtained was purified by reversed-phase silica gel column chromatography [eluent; acetonitrile:water=3:7] to give 23 mg of 4-(3-(7-methoxy-2-oxoquinolin-1(2H)-yl)propyl)-1-(3-phenylpropyl)piperidine-4-carboxylic acid as a white solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524738B2uspto-grants-2013_09