Reacción #75790

ord-2a7deb7aaaf94e27b282bb94ce521411

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe reaction mixture was filtered
  2. 2
    Otroto remove the catalyst
  3. 3
    ConcentraciónThe filtrate was concentrated under vacuum
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in dichloromethane
  5. 5
    LavadoThe dichloromethane solution was washed twice with 10% sodium hydroxide and with brine
  6. 6
    Otrodried
  7. 7
    Concentraciónconcentrated under vacuum
  8. 8
    Otroto provide crude product
  9. 9
    OtroThis material was purified by chromatography
  10. 10
    Lavadoeluting with 10% methanol in dichloromethane
  11. 11
    OtroThe resulting oil was triturated with acetonitrile

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699878B2uspto-grants-2004_03