HRID1595119

反应详情

EQUATION

反应方程式

HRID 1595119 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

15.33 g (38 mmol) of N3-(2,6-dioxomorpholinoethyl)-N6-(ethoxy-carbonylmethyl)-3,6-diazaoctanedioic acid (Example 13a of EP 0331 616) is suspended in dimethylformamide (DMF) and mixed in an ice bath with 21.07 ml (152 mmol) of triethylamine and 7.65 g (38 mmol) of 11-aminoundecanoic acid. The temperature is allowed to increase to room temperature and the reaction solution is stirred overnight. After completion of the reaction, the possibly still slightly cloudy solution is filtered and the filtrate is concentrated by evaporation in a vacuum. The residue is absorptively precipitated with ether and then recrystallized from water (17.8 g). The ethyl ester is dissolved in 2 N NaOH and is adjusted to pH 7 after 3 hours by adding Amberlite® IR 120 (H+). The ion exchange material is suctioned off, the filtrate is freeze-dried (20.1 g) and then added to H2O/methanol (2:1) on 100 ml of Amberlite® IR 120 (H+) and the acid eluate is concentrated by evaporation and recrystallized from water.

WORKUP

后处理

  1. customAfter completion of the reaction
  2. filtrationthe possibly still slightly cloudy solution is filtered
  3. concentrationthe filtrate is concentrated by evaporation in a vacuum
  4. customThe residue is absorptively precipitated with ether
  5. customrecrystallized from water (17.8 g)
  6. dissolutionThe ethyl ester is dissolved in 2 N NaOH
  7. waitis adjusted to pH 7 after 3 hours
  8. additionby adding Amberlite® IR 120 (H+)
  9. customthe filtrate is freeze-dried (20.1 g)
  10. additionadded to H2O/methanol (2:1) on 100 ml of Amberlite® IR 120 (H+)
  11. concentrationthe acid eluate is concentrated by evaporation
  12. customrecrystallized from water