HRID58323

反应详情

EQUATION

反应方程式

HRID 58323 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

590 mg of (S,E)-methyl 7-(1-(2-tert-butoxy-2-oxoethyl)-2-oxo-1,2-dihydropyridin-3-yl-amino)-6-(tert-butoxycarbonylamino)-7-oxohept-2-enoate (ZED1209, 1.20 mmol) are dissolved in 10 mL of dichloromethane and to this solution 10 mL of trifluoroacetic acid is added. It is stirred at RT for 1 h. The solvent is removed in vacuo and the residue is dried under high vacuum. The obtained oil is further reacted without purification. The oil is taken up in 15 mL of DMF and treated with 173 μL of DIPEA. By successive addition of DIPEA the pH value is adjusted to ca. 7. To this solution, 285 mg of Boc-OSu (1.1 eq) are added and stirred at RT overnight. The solvent is removed in vacuo and the residue is purified by preparative HPLC (30% ACN in water, 8 mL/min, gradient 1% pro min).

WORKUP

后处理

  1. additionis added
  2. customThe solvent is removed in vacuo
  3. customthe residue is dried under high vacuum
  4. customThe obtained oil is further reacted without purification
  5. stirringstirred at RT overnight
  6. customThe solvent is removed in vacuo
  7. customthe residue is purified by preparative HPLC (30% ACN in water, 8 mL/min, gradient 1% pro min)