反応 #2812

ord-d743b6dc42e449f9a5c576408807e9c4

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他partition between ethyl acetate (25 mL) and brine (15 mL)
  2. 2
    洗浄Wash the organic layer with brine (15 mL)
  3. 3
    乾燥dry (Na2SO4)
  4. 4
    その他purify by silica gel chromatography (1:1 hexane/ethyl acetate followed by 1:1:0.01 hexane/ethyl acetate/acetic acid)

実験手順

Dissolve 2-[4-(2-benzoylsulfanyl-3-phenyl-propionyl-amino)-3-oxo-1,3,4,5-tetrahydro-benzo[c]azepin-2-yl]-4-methyl-valeric acid, tert-butyl ester (141 mg, 0.229 mmol) in methylene chloride (5 mL) and treat with anisole (0.12 mL, 1.15 mmol) then with trifluoroacetic acid (1.5M). Stir at room temperature for 15 hours, partition between ethyl acetate (25 mL) and brine (15 mL). Wash the organic layer with brine (15 mL), dry (Na2SO4) and purify by silica gel chromatography (1:1 hexane/ethyl acetate followed by 1:1:0.01 hexane/ethyl acetate/acetic acid) to give the title compound as a white solid (157 mg).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05731306uspto-grants-1998_03