Reaktion #46023

ord-ee3372dc62ea490098f84a18483b91e6

Reaktionsgleichung

CC(C)Cc1nc(-c2ccc(OCC(=O)N3CCN(c4ccncc4)CC3)cc2)cn1-c1ccc(Oc2ccc(Cl)cc2)cc1
product
CC(C)Cc1nc(-c2ccc(OCC(=O)N3CCN(c4ccncc4)CC3)cc2)cn1-c1ccc(Oc2ccc(Cl)cc2)cc1
2-(4-{1-[4-(4-Chloro-phenoxy)-phenyl]-2-isobutyl-1H-imidazol-4-yl}-phenoxy)-1-(4-pyridin-4-yl-piperazin-1-yl)-ethanone
B.C1CCOC1
BH3-THF
CC(C)Cc1nc(-c2ccc(OCCN3CCN(c4ccncc4)CC3)cc2)cn1-c1ccc(Oc2ccc(Cl)cc2)cc1
1-[2-(4-{1-[4-(4-Chloro-phenoxy)-phenyl]-2-isobutyl-1H-imidazol-4-yl}-phenoxy)-ethyl]-4-pyridin-4-yl-piperazine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction was heated
  2. 2
    Temperaturto reflux until the reaction
  3. 3
    SonstigeThe crude product was purified by silica gel chromatography
  4. 4
    Sonstigeto afford Example 527

Vorschrift

The product of Example 522 was taken in 4 ml of THF to which was added 5 eq. of BH3-THF solution and the reaction was heated to reflux until the reaction was complete. The crude product was purified by silica gel chromatography to afford Example 527.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737285B2uspto-grants-2010_06