HRID1775835

反应详情

EQUATION

反应方程式

HRID 1775835 的结构方程式

PROCEDURE

实验过程

To tert-butyl 4-(4-(heptyloxy)phenyl)-3-oxopiperazine-1-carboxylate (540 mg, 1.38 mmol) was added 4M HCl in dioxane (2.07 mL, 8.30 mmol). The reaction mixture was stirred at room temperature for 2 h. The precipitate was filtered, washed with hexane (5 mL) and dried. The crude product was purified by column chromatography (79/20/1 DCM/MeOH/NH4) to afford 325 mg (80%) of 1-(4-(heptyloxy)phenyl)piperazin-2-one as a colorless solid. LCMS-ESI (m/z) calculated for C17H26N2O2: 290.4. found 291.0 [M+H]+, tR=1.49 min. (Method 4).

WORKUP

后处理

  1. filtrationThe precipitate was filtered
  2. washwashed with hexane (5 mL)
  3. customdried
  4. customThe crude product was purified by column chromatography (79/20/1 DCM/MeOH/NH4)