Reaktion #75790
ord-2a7deb7aaaf94e27b282bb94ce521411
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1FiltrationThe reaction mixture was filtered
- 2Sonstigeto remove the catalyst
- 3EinengenThe filtrate was concentrated under vacuum
- 4workup.DISSOLUTIONThe residue was dissolved in dichloromethane
- 5WaschenThe dichloromethane solution was washed twice with 10% sodium hydroxide and with brine
- 6Sonstigedried
- 7Einengenconcentrated under vacuum
- 8Sonstigeto provide crude product
- 9SonstigeThis material was purified by chromatography
- 10Wascheneluting with 10% methanol in dichloromethane
- 11SonstigeThe 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.