HRID1359360

反应详情

EQUATION

反应方程式

HRID 1359360 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 3.0 g of 2-benzyl-3-iodo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine, 1.07 g of (3R)-3-ethynyl-3-quinuclidinol, 82 mg of tetrakis(triphenylphosphine)palladium (0), 68 mg of cuprous iodide, 2.0 ml of triethylamine and 7 ml of methanol was stirred at room temperature overnight in a nitrogen atmosphere. The reaction solution was partitioned between aqueous dilute ammonia-ethyl acetate, washed with washed with water, dried over anhydrous magnesium sulfate and then concentrated. 10 ml of tetrahydrofuran was added to the residue to dissolve under heating, and to the mixture was added 15 ml of ethyl acetate. The mixture was filtered through 10 g of NH-silica gel, washed with ethyl acetate, and concentrated. The residue was crystallized from ethyl acetate, to give 2.79 g of the target compound.

WORKUP

后处理

  1. customThe reaction solution was partitioned between aqueous dilute ammonia-ethyl acetate
  2. washwashed
  3. washwith washed with water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated
  6. addition10 ml of tetrahydrofuran was added to the residue
  7. dissolutionto dissolve
  8. temperatureunder heating
  9. additionto the mixture was added 15 ml of ethyl acetate
  10. filtrationThe mixture was filtered through 10 g of NH-silica gel
  11. washwashed with ethyl acetate
  12. concentrationconcentrated
  13. customThe residue was crystallized from ethyl acetate