반응 #1964624

ord-26725bbae2b44aba84b559bff6d73e75

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타obtained
  2. 2
    기타After treatment and purification as in stage 3 of Example 3, 40 mg of 2-cyclohexylamino-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]benzamide
  3. 3
    기타are thus obtained in the form of a white solid

실험 절차

The process is carried out as in stage 3 of Example 3, but using 100 mg of 2-fluoro-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-carbazol-9-yl]benzonitrile, obtained according to stage 2 of Example 3, 263 mg of potassium carbonate and 94 mg of cyclohexylamine in 0.8 ml of dimethyl sulphoxide. 0.4 ml of a 1M aqueous solution of sodium hydroxide, 0.4 ml of a 30% aqueous solution of hydrogen peroxide and 2 ml of ethanol are then added to the reaction medium. After treatment and purification as in stage 3 of Example 3, 40 mg of 2-cyclohexylamino-4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]benzamide are thus obtained in the form of a white solid, the characteristics of which are the following:

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08309721B2uspto-grants-2012_11