HRID64482

反应详情

EQUATION

反应方程式

HRID 64482 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of 250 mg of 8-(cyclohexylmethoxy)-2-methyl-N-[(3S)-piperidin-3-yl]imidazo[1,2-a]pyridine-3-carboxamide dihydrochloride in 10 ml of methanol were added 157 μl of triethylamine, 300 mg of Molecular Sieves 3A, 323 μl of acetic acid, 1.53 ml of [(1-ethoxy cyclopropyl)oxy](trimethyl)silane, and 146 mg of sodium cyanoborohydride under ice-cooling, followed by stirring for 6 hours under heating to reflux. The insoluble material was removed by filtration and the filtrate was concentrated under reduced pressure. To the obtained residue were added saturated aqueous sodium bicarbonate and chloroform to carry out a layer separation operation. The organic layer was dried over anhydrous sodium sulfate, the solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography. To a mixture of the obtained purified product, ethyl acetate, and methanol was added a 4 M hydrogen chloride/ethyl acetate solution under ice-cooling, and the solvent was evaporated under reduced pressure. To the obtained residue was added ethyl acetate and hexane, followed by stirring. The resulting solid was collected by filtration and dried to obtain 136 mg of 8-(cyclohexylmethoxy)-N-[(3S)-1-cyclopropylpiperidin-3-yl]-2-methylimidazo[1,2-a]pyridine-3-carboxamide dihydrochloride.

WORKUP

后处理

  1. temperaturecooling
  2. temperatureunder heating to reflux
  3. customThe insoluble material was removed by filtration
  4. concentrationthe filtrate was concentrated under reduced pressure
  5. additionTo the obtained residue were added saturated aqueous sodium bicarbonate and chloroform
  6. customa layer separation operation
  7. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  8. customthe solvent was evaporated under reduced pressure
  9. customthe obtained residue was purified by silica gel column chromatography
  10. additionTo a mixture of the obtained
  11. custompurified product, ethyl acetate, and methanol
  12. additionwas added a 4 M hydrogen chloride/ethyl acetate solution under ice-
  13. temperaturecooling
  14. customthe solvent was evaporated under reduced pressure
  15. additionTo the obtained residue was added ethyl acetate and hexane
  16. stirringby stirring
  17. filtrationThe resulting solid was collected by filtration
  18. customdried