HRID2390273

反应详情

EQUATION

反应方程式

HRID 2390273 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A mixture of (1-bromo-naphthalen-2-yloxy)-acetic acid tert-butyl ester (Intermediate 217; 500 mg; 1.48 mmol), 1-ethynyl-3-(propane-1-sulfonyl)-benzene (618 mg; 2.97 mmol) and PPh3 (39 mg; 0.15 mmol) in water (4.40 ml) and Acetone (5.6 ml) was treated with palladium(II) chloride (13 mg; 0.07 mmol) and piperidine (295 μl; 2.97 mmol) and heated at 60° C. for 2 days. The reaction mixture was extracted with EtOAc, the organic phase was dried over MgSO4 and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography (silica), eluting with cyclohexane containing increasing amounts of EtOAc to give the title compound as a yellow sticky solid.

WORKUP

后处理

  1. extractionThe reaction mixture was extracted with EtOAc
  2. dry with materialthe organic phase was dried over MgSO4
  3. concentrationconcentrated under reduced pressure
  4. customThe resulting residue was purified by flash column chromatography (silica)
  5. washeluting with cyclohexane containing
  6. temperatureincreasing amounts of EtOAc