HRID1991552

反应详情

EQUATION

反应方程式

HRID 1991552 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 benzyl 4-{[(2R,3S)-3-(acetylamino)-4-(3,5-difluorophenyl)-2-hydroxybutyl]amino}-6-neopentyl-3,4-dihydroquinoline-1(2H)-carboxylate (0.242 g) in EtOH (30 mL) was added 1N HCl (1.0 mL) and 10% palladium on carbon (0.030 g). The mixture was degassed with N2 for five minutes. The mixture was placed on a hydrogenation apparatus under 47 psi of H2 and was shaken for 4.5 hours. The palladium was filtered off using Celite and the solvent was concentrated under reduced pressure. The residue was then partitioned between water and ethyl acetate and the organic layers were washed with aqueous sodium bicarbonate, dried with magnesium sulfate, filtered, and concentrated. A silica gel column using 4% MeOH in dichloromethane with 0.25% NH4OH as the solvent solution gave 0.095 g of the title compound. MS (ESI+) for C26H35F2N3O2 m/z 460.27 (M+H)+.

WORKUP

后处理

  1. customThe mixture was degassed with N2 for five minutes
  2. filtrationThe palladium was filtered off
  3. concentrationthe solvent was concentrated under reduced pressure
  4. customThe residue was then partitioned between water and ethyl acetate
  5. washthe organic layers were washed with aqueous sodium bicarbonate
  6. dry with materialdried with magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated