반응 #1589730

ord-62d0add5149f4c43b15c2ec1d9af7abc

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooling
  2. 2
    기타After completion of the reaction
  3. 3
    기타the solvent was evaporated
  4. 4
    기타the residue was precipitated with acetonitrile (10 ml)
  5. 5
    기타purified by silica gel column chromatography (chloroform/ethyl acetate=10:1)

실험 절차

Methyl 4-amino-2-methoxybenzoate (79 mg, 0.44 mmol) was dissolved in chloroform (1 ml), and HOBt (7 mg, 0.05 mmol) and 3,4,5-tris(octadecyloxy)cyclohexylcarboxylic acid (201 mg, 0.22 mmol) were added. EDC.HCl (45 mg, 0.23 mmol) was added under ice-cooling, and the mixture was stirred at room temperature overnight. After completion of the reaction, the solvent was evaporated, and the residue was precipitated with acetonitrile (10 ml), and then purified by silica gel column chromatography (chloroform/ethyl acetate=10:1) to give N-(3-methoxy-4-methoxycarbonylphenyl) 3,4,5-tris(octadecyloxy)cyclohexylcarboxamide (70 mg, 0.06 mmol, yield 27%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09206230B2uspto-grants-2015_12