HRID1614654

反应详情

EQUATION

反应方程式

HRID 1614654 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 4-[[(3,4-difluorophenyl)amino](4-fluorophenyl)methyl]piperidine (5.41 g, 0.0169 mol), 1-(2-bromoethoxy)naphthalene (4.23 g, 0.0169 mol) and sodium bicarbonate (5.53 g, 0.059 mol) in 350 mL of 1-butanol containing sodium iodide (0.2 g) was heated 20 h at reflux. The reaction was concentrated to dryness and partitioned between chloroform and water. The chloroform layer was washed with 5% sodium hydroxide and dried (Na2SO4). Chloroform was removed to give a brown oil. The oil was dissolved in methylene chloride and placed on a silica gel column for flash chromatography. Elution was accomplished using 1% methanol-methylene chloride and 2% methanol-methylene chloride. Fractions of similar purity were combined and solvents removed to give a fluffy grey material. This material was converted to the HCl salt and the salt was recrystallized from methanol-diethyl ether to give a whitish-grey solid. The material was dried 16 h in vacuo at 80° C. This process provided 5.06 g (53.1%) of greyish material, mp 212°-215° C. (dec).

WORKUP

后处理

  1. temperaturewas heated 20 h
  2. temperatureat reflux
  3. concentrationThe reaction was concentrated to dryness
  4. custompartitioned between chloroform and water
  5. washThe chloroform layer was washed with 5% sodium hydroxide
  6. dry with materialdried (Na2SO4)
  7. customChloroform was removed
  8. customto give a brown oil
  9. washElution
  10. customsolvents removed
  11. customto give a fluffy grey material
  12. customthe salt was recrystallized from methanol-diethyl ether
  13. customto give a whitish-grey solid
  14. customThe material was dried 16 h in vacuo at 80° C