HRID625272

反应详情

EQUATION

反应方程式

HRID 625272 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of 10.5 mg of methyl 1H-indole-4-carboxylate, 18.2 mg of 2-(2-(3-(chloromethyl)benzamido)-5-(piperidin-1-yl)phenyl)-N-(3-(trifluoromethyl)benzyl)-isonicotinamide 8.1a, and excess potassium carbonate in 300 μL of DMF was stirred for 24 h. The solvent was evaporated and the residue was purified by silica gel chromatography. The product was dissolved in 1 mL of 4:1 THF/water and treated with 10 mg of LiOH.H2O. After stirring 4 days at 70° C. the reaction mixture was acidified with 3.0 N hydrochloric acid and then extracted with ethyl acetate. The aqueous phase was washed with ethyl acetate, and the combined organic extracts washed with brine and dried (NaSO4). The residue was purified by reverse phase HPLC eluting with 0.1% TFA in a water/acetonitrile gradient to give 10.6 mg of product. MS (ES, m/z) 732.4 [M+H]+.

WORKUP

后处理

  1. customThe solvent was evaporated
  2. customthe residue was purified by silica gel chromatography
  3. dissolutionThe product was dissolved in 1 mL of 4:1 THF/water
  4. additiontreated with 10 mg of LiOH.H2O
  5. stirringAfter stirring 4 days at 70° C. the reaction mixture
  6. extractionextracted with ethyl acetate
  7. washThe aqueous phase was washed with ethyl acetate
  8. washthe combined organic extracts washed with brine
  9. dry with materialdried (NaSO4)
  10. customThe residue was purified by reverse phase HPLC
  11. washeluting with 0.1% TFA in a water/acetonitrile gradient