Reacción #75790
ord-2a7deb7aaaf94e27b282bb94ce521411
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1FiltraciónThe reaction mixture was filtered
- 2Otroto remove the catalyst
- 3ConcentraciónThe filtrate was concentrated under vacuum
- 4workup.DISSOLUTIONThe residue was dissolved in dichloromethane
- 5LavadoThe dichloromethane solution was washed twice with 10% sodium hydroxide and with brine
- 6Otrodried
- 7Concentraciónconcentrated under vacuum
- 8Otroto provide crude product
- 9OtroThis material was purified by chromatography
- 10Lavadoeluting with 10% methanol in dichloromethane
- 11OtroThe 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.