HRID2357585

反应详情

EQUATION

反应方程式

HRID 2357585 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A mixture of 3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide (0.11 g, 0.327 mmol), 2-chlorophenylboronic acid (51 mg, 329 μmol), 5 mL DME/EtOH (4:1), 0.5 mL 2M K2CO3 and tetrakis(triphenylphosphine)palladium (20mg) was stirred at 90° C. for 1 h. The reaction mixture was cooled to RT. The crude product was purified via flash chromatography (silica gel) with 2% 2 M ammonia in MeOH/DCM to 6% 2 M ammonia in MeOH/DCM to give the crude compound (120 mg) as a yellow solid. The compound was further purified by HPLC by dissolving the crude product in methanol (˜20 mg/mL) and injecting at a rate of about 0.500 mL per injection onto the Gilson preparatory HPLC. Pure product fractions were collected, combined, basefied with sodium bicarbonate (saturated, aqueous), extracted with CH2Cl2, separated, dried over sodium sulfate, and concentrated via rotary evaporation to give pure title compound (28.8 mg) as a white solid.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled to RT
  2. customThe crude product was purified via flash chromatography (silica gel) with 2% 2 M ammonia in MeOH/DCM to 6% 2 M ammonia in MeOH/DCM
  3. customto give the crude compound (120 mg) as a yellow solid
  4. customThe compound was further purified by HPLC
  5. dissolutionby dissolving the crude product in methanol (˜20 mg/mL)
  6. customPure product fractions were collected
  7. extractionextracted with CH2Cl2
  8. customseparated
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated via rotary evaporation