HRID1773098

反应详情

EQUATION

反应方程式

HRID 1773098 的结构方程式

PROCEDURE

实验过程

To 127 mg (0.5 mmol) of (2S)-3-amino-2-{[(tert-butoxy)carbonyl]amino}propanoic acid methylester hydrochloride, 87 mg (0.5 mmol) of 3-aminobenzenesulfonic acid and 97 mg (0.6 mmol) of N,N-carbonyl diimidazole, 1 ml of methylene chloride and 1 ml of tetrahydrofuran were added and stirred at room temperature overnight. After distilling the solvent away, purification was carried out using purification step A to obtain a crude purified substance of the title compound in protected form. To the obtained crude purified substance, 1 ml of methylene chloride and 1 ml of trifluoroacetic acid were added and stirred at room temperature for 5 hours. After distilling the solvent away, purification was carried out by purification step A to obtain the title compound.

WORKUP

后处理

  1. distillationAfter distilling the solvent away
  2. custompurification
  3. custompurification step A
  4. customto obtain a crude
  5. custompurified substance of the title compound in protected form
  6. customTo the obtained crude
  7. custompurified substance, 1 ml of methylene chloride and 1 ml of trifluoroacetic acid
  8. additionwere added
  9. stirringstirred at room temperature for 5 hours
  10. distillationAfter distilling the solvent away
  11. custompurification
  12. customwas carried out by purification step A