Reaktion #1938464

ord-10b308f7e25c4ee7b87c81629f48adc5

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe compound is prepared in analogy to example 33.0
  2. 2
    SonstigeAfter the usual work-up and purification 201 mg (58.9%) of the title compound
  3. 3
    Sonstigeare obtained

Vorschrift

The compound is prepared in analogy to example 33.0. 216 mg (0.756 mmol) 2-Piperidine-4-ylquinoxaline are reacted with 200 mg (0.63 mmol) 4-[6-(4-fluorophenyl)-imidazo[1,2-a]pyrimidin-7-yl]-benzaldehyde. After the usual work-up and purification 201 mg (58.9%) of the title compound are obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08957064B2uspto-grants-2015_02