Reacción #479595

ord-b7574dc8e00f479ba6c5c2eadaa604d4

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otropurifying via preparative HPLC
  2. 2
    Lavadoeluting with 90:10 to 80:20 DCM/ethyl acetate

Procedimiento

Using the procedure of Example 342 using N-(3-bromophenyl)pyridin-3-ylmethylamine and 2-phenylphenol (Aldrich) and purifying via preparative HPLC eluting with 90:10 to 80:20 DCM/ethyl acetate gave N-(3-(2-phenylphenoxy)phenyl)pyrid-3-ylmethylamine. Anal Calcd for C24H20N2O.0.2H2O: C, 80.96; H, 5.78; N, 7.87. Found: C, 81.07; H, 5.73; N, 7.63. MS found 353.1 [M+H]+

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06800651B2uspto-grants-2004_10