HRID1177884

反应详情

EQUATION

反应方程式

HRID 1177884 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

DIPEA (77 mg, 0.1 mL, 0.59 mmol) was added to a stirred solution of 4-pyrimidin-2-yl-benzoic acid (40 mg, 0.19 mmol) in DMF (2 mL). HOBT (32 mg, 0.23 mmol) and EDCI (46 mg, 0.23 mmol) were then added at room temperature. After 2 minutes 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone hydrochloride salt (84 mg, 0.23 mmol) was added and the resulting mixture was stirred at room temperature overnight. Cold water was then added and then extrated with ethyl acetate. The organic layer was washed with brine and dried over Na2SO4 and concentrated under reduced pressure to afford 30 mg (30.9%) of N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-4-pyrimidin-2-yl-benzamide. LCMS Purity: 97.15%. 1H NMR (DMSO-d6): δ 9-8.9 (d, 2H), 8.8-8.7 (m, 1H), 8.5 (d, 2H), 8.1-8.0 (d, 2H), 7.9-7.5 (m, 5H), 4.3-4.1 (m, 2H), 3.8-3.5 (m, 4H), 3.5-3.4 (m, 2H), 3.2-3.0 (m, 2H).

WORKUP

后处理

  1. washThe organic layer was washed with brine
  2. dry with materialdried over Na2SO4
  3. concentrationconcentrated under reduced pressure