反応 #54313

ord-dbca350db4ff403ca0a0c18ad91427fb

反応条件

温度
25°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITThis solution is kept overnight at 25° C.
  2. 2
    洗浄washed with water
  3. 3
    その他dried
  4. 4
    その他evaporated to dryness
  5. 5
    workup.ADDITIONThe residue is treated with 5 ml of a 40% (w/w) solution of hydrogen bromide in dioxane at 25° C. for 30 minutes
  6. 6
    workup.ADDITIONEther (50 ml) is then added
  7. 7
    その他the precipitate collected
  8. 8
    workup.ADDITIONThis is then treated with 20 ml of a 1 N sodium hydroxide solution overnight at 25° C.
  9. 9
    洗浄Elution with 2 N ammonium hydroxide

実験手順

To 2-(benzyloxycarbonyl)amino-2-vinylglutaric acid (305 mg, 1 mM) in methylene chloride (15 ml) is added triethylamine (205 mg, 2 mM) followed by ethyl chloroformate (218 mg, 2 mM). The solution is stirred for one hour at 25° C., then alanine methyl ester (206 mg, 2 mM) in methylene chloride (5 ml) is added. This solution is kept overnight at 25° C., washed with water, dried and evaporated to dryness. The residue is treated with 5 ml of a 40% (w/w) solution of hydrogen bromide in dioxane at 25° C. for 30 minutes. Ether (50 ml) is then added and the precipitate collected. This is then treated with 20 ml of a 1 N sodium hydroxide solution overnight at 25° C., the pH adjusted to 6.5, and applied to an Amberlite 120 H+ resin. Elution with 2 N ammonium hydroxide afforded 5-amino-2,10-dimethyl-4,8-dioxo-5-vinyl-3,9-diazaundecanedioic acid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04147873uspto-grants-1979_04