HRID1047763

反应详情

EQUATION

反应方程式

HRID 1047763 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of 2-(2-iodo-3-methyl-benzoylamino)-indan-2-carboxylic acid ethyl ester (693 mg, 1.54 mmol) in anhydrous DMF (5 mL) and DIPA (diisopropylamine, 10 mL) is added Pd(PPh3)4 (89 mg, 7.7% mmol), CuI (29 mg, 0.154 mmol) and pent-1-yne (1.5 mL, 15.4 mmol). The resulting solution is covered in argon and run in a microwave reaction: 110° C., 35 minutes. After the removal of DMF and DIPA in vacuo, the residue is dissolved in EtOAc (100 mL) and washed with water (1×10 mL) and brine (2×10 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (120 g silica gel, gradient elution: 0%-40% EtOAc in heptane) to give a pure product (122) as a pale yellow solid (144 mg, 24%).

WORKUP

后处理

  1. customrun in a microwave reaction
  2. custom110° C., 35 minutes
  3. customAfter the removal of DMF and DIPA in vacuo
  4. dissolutionthe residue is dissolved in EtOAc (100 mL)
  5. washwashed with water (1×10 mL) and brine (2×10 mL)
  6. dry with materialThe organic layer is dried over anhydrous Na2SO4
  7. concentrationconcentrated in vacuo
  8. customThe residue is purified by flash column chromatography (120 g silica gel, gradient elution: 0%-40% EtOAc in heptane)