HRID1023596

反应详情

EQUATION

反应方程式

HRID 1023596 反应方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

N1-(4-{[2-methyl-5-(methyloxy)phenyl]oxy}phenyl)-D-alaninamide (Intermediate 16, 118 mg) was dissolved in dry dichloromethane (18 mL). The reaction mixture was cooled down in an ice bath. Triethylamine 0.327 mL, 2.350 mmol) was added. Then a solution of triphosgene in dry dichloromethane (46.5 mg, 0.157 mmol) dissolved in 7 mL of dichloromethane was added. The reaction was stirred at 0° C. for 10 min under argon. A saturated aqueous solution of NaHCO3 was added (18 mL) and the aqueous layer was extracted with dichloromethane 4 times (4×15 mL). After drying over sodium sulphate, the solvents were removed under vacuum. The residue was purified by silica gel chromatography (Companion system, 12 g cartridge) eluting with a gradient cHex/EOAc from to 100/0 to 60/40 during 20 min and 60/40 during 30 min. This afforded the title compound (91 mg).

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled down in an ice bath
  2. additionwas added
  3. extractionthe aqueous layer was extracted with dichloromethane 4 times (4×15 mL)
  4. dry with materialAfter drying over sodium sulphate
  5. customthe solvents were removed under vacuum
  6. customThe residue was purified by silica gel chromatography (Companion system, 12 g cartridge)
  7. washeluting with a gradient cHex/EOAc from to 100/0 to 60/40 during 20 min
  8. wait60/40 during 30 min