HRID17872

反应详情

EQUATION

反应方程式

HRID 17872 的结构方程式

PROCEDURE

实验过程

To trifluoroacetic acid (1 mL) at room temperature was added benzyl-4-(3-hydroxy-6-methoxy-2-methyl-1-oxo-4-phenyl-1,2,3,4-tetra-hydroisoquinolin-3-yl)piperidine-1-carboxylate (215 mg, 0.443 mmol) with stirring. After 10 min. the reaction mixture was made basic with 2N sodium hydroxide, extracted with methylene chloride (3×) and dried with anhydrous sodium sulfate. Filtration followed by evaporation of solvent in vacuo gave a solid which was triturated with hexane-ethyl acetate to afford benzyl-4-(6-methoxy-2-methyl-1-oxo-4-phenyl-1,2-dihydroisoquinolin-3-yl)piperidine-1-carboxylate as a solid (141 mg, 0.292 mmol, 66%). MS [M+H]+ 483.2

WORKUP

后处理

  1. extractionextracted with methylene chloride (3×)
  2. dry with materialdried with anhydrous sodium sulfate
  3. filtrationFiltration
  4. customfollowed by evaporation of solvent in vacuo
  5. customgave a solid which
  6. customwas triturated with hexane-ethyl acetate