HRID1499894

反应详情

EQUATION

反应方程式

HRID 1499894 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

CONDITIONS

反应条件

温度
120 °C

PROCEDURE

实验过程

A mixture of 5-bromo-N,N-dimethylpyridine-2-carboxamide (23 g, 98 mmol), 4,4,5,5,4′,4′,5′,5′-octamethyl-[2,2′]bi[[1,3,2]dioxaborolanyl] (27 g, 110 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (Aldrich, Catalog No. 379670) (1:1) (4.8 g, 5.9 mmol), 1,1′-bis(diphenylphosphino)ferrocene (Aldrich, Catalog No. 177261) (3.3 g, 5.9 mmol), and potassium acetate (30 g, 300 mmol) in 1,4-dioxane (600 mL) was degassed with nitrogen and was heated at 120° C. for 16 hrs. The mixture was cooled to room temperature and diluted with ethyl acetate (600 mL) and water (600 mL). The aqueous layer was concentrated in vacuo to give a solid residue. The solids were taken up in acetonitrile and filtered to remove the residual insoluble salts. The acetonitrile was removed in vacuo to give {6-[(dimethylamino)carbonyl]pyridin-3-yl}boronic acid (12 g, 60%). LCMS calculated for C8H12BN2O3 (M+H)+: m/z=195.1; found: 195.1.

WORKUP

后处理

  1. customwas degassed with nitrogen
  2. temperatureThe mixture was cooled to room temperature
  3. additiondiluted with ethyl acetate (600 mL) and water (600 mL)
  4. concentrationThe aqueous layer was concentrated in vacuo
  5. customto give a solid residue
  6. filtrationfiltered
  7. customto remove the residual insoluble salts
  8. customThe acetonitrile was removed in vacuo