HRID910966

反应详情

EQUATION

反应方程式

HRID 910966 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

A 3 dram vial was charged with 3-(2-(4-methylthiazol-2-ylamino)pyridin-4-yloxy)benzoic acid (0.1 g, 0.3055 mmol), triethylamine (0.2129 mL, 1.527 mmol) and THF (2 mL), and the reaction mixture was cooled to 0° C. Ethyl carbonochloridate (0.03359 mL, 0.3513 mmol) was added and the reaction mixture was stirred at 0° C. for 30 minutes. 1-Ethylpiperazine (0.1164 mL, 0.9164 mmol) was added and the reaction mixture was warmed to room temperature and stirred for 1 hour, and then 2N NaOH was added. The reaction mixture was extracted with ethyl acetate, dried over magnesium sulfate, filtered and concentrated. The residue was purified using prepacked silica gel column with 5% methanol in DCM as eluent to afford the desired product (0.085 g, 56.05% yield) as off white solid. Mass spectrum (esi) m/z=424 (100) (M+H-2HCl).

WORKUP

后处理

  1. temperaturethe reaction mixture was warmed to room temperature
  2. stirringstirred for 1 hour
  3. extractionThe reaction mixture was extracted with ethyl acetate
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was purified