HRID471753

反应详情

EQUATION

反应方程式

HRID 471753 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a stirred solution of trimethyl(prop-2-ynyl)silane (1.12 g, 10 mmol), 2-amino-6-bromobenzonitrile (Klaubert, D. H.; Sellstedt, J. H.; Guinosso, C. J.; Capetola, R. J.; Bell, S. C. J. Med. Chem. 1981, 24, 742) (1.0 g, 5 mmol), CuI (0.01 equiv.) in triethylamine (50 mL) was added Pd(PPh3)4 (0.1 equiv.) at room temperature under nitrogen. The reaction mixture was then refluxed under nitrogen overnight. The solvent was evaporated, and the residue was titrated with EtOAc/water. The organic layer was separated, were washed with brine, and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel eluting with 15% EtOAc in hexanes to give the title compound (1.43 g, 63%) as a as a liquid. MS 229 (MH+).

WORKUP

后处理

  1. temperatureThe reaction mixture was then refluxed under nitrogen overnight
  2. customThe solvent was evaporated
  3. customThe organic layer was separated
  4. washwere washed with brine
  5. dry with materialdried over Na2SO4
  6. customAfter evaporation of the solvent
  7. customthe residue was purified by chromatography on silica gel eluting with 15% EtOAc in hexanes