HRID530327

反应详情

EQUATION

反应方程式

HRID 530327 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
85 °C

PROCEDURE

实验过程

In a 50 ml round-bottomed flask, (rac)-4-bromo-6,7-dihydro-5H-cyclopenta[c]pyridin-7-amine (intermediate A-3[C]) (107 mg, 500 μmol) and 1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one (intermediate A-1) (172 mg, 600 μmol) were dissolved in EtOH (9 mL) to give a brown solution. Na2CO3 (58.3 mg, 550 μmol), dissolved in water (1.5 mL) was added followed by tetrakis(triphenylphosphine)palladium (0) (17.3 mg, 15.0 mmol) after evacuation and replacing 5 times with Argon. The suspension was then heated at 85° C. overnight. A aq. 10% NaCl solution was added at RT, and the mixture was extracted with AcOEt (3×). The organic fractions were washed again with aq. 10% NaCl solution, dried over Na2SO4, filtered, evaporated and purified by flash chromatography (50 g SiO2, Telos-cartridge, CH2Cl2/MeOH (2%)) to afford the title compound (21 mg, 14%) as a dark green powder. MS: 294.2 (M+H+)

WORKUP

后处理

  1. customto give a brown solution
  2. additionwas added
  3. extractionthe mixture was extracted with AcOEt (3×)
  4. washThe organic fractions were washed again with aq. 10% NaCl solution
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customevaporated
  8. custompurified by flash chromatography (50 g SiO2, Telos-cartridge, CH2Cl2/MeOH (2%))