Reaktion #75790

ord-2a7deb7aaaf94e27b282bb94ce521411

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction mixture was filtered
  2. 2
    Sonstigeto remove the catalyst
  3. 3
    EinengenThe filtrate was concentrated under vacuum
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in dichloromethane
  5. 5
    WaschenThe dichloromethane solution was washed twice with 10% sodium hydroxide and with brine
  6. 6
    Sonstigedried
  7. 7
    Einengenconcentrated under vacuum
  8. 8
    Sonstigeto provide crude product
  9. 9
    SonstigeThis material was purified by chromatography
  10. 10
    Wascheneluting with 10% methanol in dichloromethane
  11. 11
    SonstigeThe resulting oil was triturated with acetonitrile

Vorschrift

A solution of N1-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-di-(1,1-dimethylethyl)-4-hydroxybenzamide (0.1 g, 0.19 mmol) in trifluoroacetic acid (15 mL) and platinum oxide (0.1 g) were combined and hydrogenated overnight on a Parr apparatus. The reaction mixture was filtered to remove the catalyst. The filtrate was concentrated under vacuum. The residue was dissolved in dichloromethane. The dichloromethane solution was washed twice with 10% sodium hydroxide and with brine, dried and then concentrated under vacuum to provide crude product. This material was purified by chromatography eluting with 10% methanol in dichloromethane. The resulting oil was triturated with acetonitrile to provide 0.05 g of N1-[2-(4-amino-2-butyl-6,7,8,9-tetrahydro-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-3,5-di-(1,1-dimethylethyl)-4-hydroxybenzamide as a white powder, m.p. 208-210° C. Analysis: Calculated for C30H44N6O2+0.1 CF3CO2H: %C, 68.17; %H, 8.35; %N, 15.79; Found: %C, 68.48; %H, 8.29; %N, 16.08.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06699878B2uspto-grants-2004_03