Reaktion #1938449

ord-4a552c98376c42ea86bd641b2c3fd202

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGBecause after one hour stirring at room temperature the reaction
  2. 2
    workup.STIRRINGafter stirring at room temperature for 70 hours
  3. 3
    SonstigeAfter purification 28 mg of the desired material
  4. 4
    Sonstigehas been obtained

Vorschrift

252 mg (1.06 mmol) 2-piperidine-4-yl-3H-imidazo[4,5-c]pyridine and 250 mg (0.84 mmol) 4-(6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde were reacted as described in example 12.0. Additional NaBH(OAc)3 has been added after one, three and five hours (two equivalents each) and the reaction mixture has been stirred overnight at room temperature. Since the reaction has not been complete, 20 mL THF and 10 mL acetic acid were added. Another two equivalents of NaBH(OAc)3 were added. Because after one hour stirring at room temperature the reaction has not changed additional 126 mg 2-piperidine-4-yl-3H-imidazo[4,5-c]pyridine and another two equivalents of NaBH(OAc)3 were added. The reaction has been worked up after stirring at room temperature for 70 hours. After purification 28 mg of the desired material has been obtained.

Quelle

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