반응 #75788

ord-9677707f760c4049af1e01e6d1aea547

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도heated on a steam bath for 30 minutes
  2. 2
    온도to cool
  3. 3
    기타The resulting precipitate was isolated by filtration
  4. 4
    기타dried
  5. 5
    기타to provide 0.15 g of N1-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-2-amino -4-methylpentamide as a white solid, m.p.60-65° C

실험 절차

1,1-Dimethylethyl N-[1-({[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]amino}carbonyl)-3-methylbutyl]carbamate (0.35 g, 0.7 mmol) was combined with 1 N hydrochloric acid (40 mL) and heated on a steam bath for 30 minutes. The reaction mixture was allowed to cool and then it was made basic with 10% sodium hydroxide. The resulting precipitate was isolated by filtration and dried to provide 0.15 g of N1-[2-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethyl]-2-amino -4-methylpentamide as a white solid, m.p.60-65° C. Analysis: Calculated for C21H31N7O: %C, 63.27; %H, 7.86; %N, 24.66. Found: %C, 62.27; %H, 7.67; %N, 24.77. HRMS (EI) calcd for C21H31N7O (M+) 397.2590 found 397.2582.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06699878B2uspto-grants-2004_03