Reaktion #7888

ord-51f0adc9d41543e1b9f0d008ab664d0d

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevacuated
  2. 2
    workup.ADDITIONToluene (600 μL) was added
  3. 3
    Sonstigethe mixture was degassed with a stream of argon for 5 min
  4. 4
    SonstigeThe tube was sealed
  5. 5
    Sonstigepurified by automated flash chromatography

Vorschrift

2-[4-(5-chloropyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazole (100 mg, 0.30 mmol), benzophenone imine (60 μL, 0.36 mmol), Pd2(dba)3 (15 mg, 0.015 mmol), 1,1′-biphenyl-2-yl(dicyclohexyl)phosphine (10 mg, 0.015 mmol), NaOtBu (40 mg, 0.42 mmol) were combined in a sealable tube evacuated and backfilled with argon. Toluene (600 μL) was added and the mixture was degassed with a stream of argon for 5 min. The tube was sealed and the mixture was heated to 80° C. for 24 h. Crude mixture was adsorbed onto silica gel and purified by automated flash chromatography using an EtOAc/hexanes gradient to afford 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N-(diphenylmethylene)pyridin-3-amine as a yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087601B2uspto-grants-2006_08