HRID233212

反应详情

EQUATION

反应方程式

HRID 233212 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.5 g, 16 mmol), K2CO3 (2.2 g, 16 mmol), KI (200 mg), 4-(3-chloropropoxy)indole (3.0 g, 14 mmol) and CH3CN (100 ml) was stirred at reflux under N2 for 7 hours and then at ambient temperature for 68 hours. Reflux was resumed for an additional 6 hours whereupon a TLC revealed incomplete reaction. K2CO3 (0.5 g, 4 mmol) was added and the reaction was stirred at reflux for 17 hours. The cooled reaction was poured into H2O and the aqueous mixture was extracted with EtOAc. The organic extract was washed with H2O and saturated NaCl and after drying over MgSO4 the solvent was removed to afford 5.7 g of a beige solid. The product was purified by preparative HPLC (Water's Associates Prep LC/System 500 using 2 silica gel columns and 4% MeOH-CH2Cl2 as eluent) to yield 3.4 g (61%) of a beige solid. Two consecutive recrystallizations from EtOH provided 2.3 g (41%) of a white powder, m.p.=129°-131° C. ANALYSIS: Calculated for C23H24FN3O2 : 70.21%C 6.15%H 10.68%N Found: 69.90%C 6.15%H 10.65%N

WORKUP

后处理

  1. temperatureat reflux under N2 for 7 hours
  2. temperatureReflux
  3. waitwas resumed for an additional 6 hours whereupon a TLC
  4. customreaction
  5. stirringthe reaction was stirred
  6. temperatureat reflux for 17 hours
  7. customThe cooled reaction
  8. extractionthe aqueous mixture was extracted with EtOAc
  9. extractionThe organic extract
  10. washwas washed with H2O and saturated NaCl
  11. dry with materialafter drying over MgSO4 the solvent
  12. customwas removed