HRID397757

反应详情

EQUATION

反应方程式

HRID 397757 的结构方程式

PROCEDURE

实验过程

A suspension of Nα-isobutyl-Nα-(4-methylbenzenesulfonyl)-L-lysine hydrochloride (600 mg) in THF (20 mL) was treated with a 1N NaOH (1.5 mL) to pH 10. A solution of commercially available Nα-(4-methylbenzenesulfonyl)-L-phenylalanine acid chloride (250 mg) in dry THF 20 mL) was added to the suspension and stirred for 2 h. Afterwards, water (2 mL) was added resulting in a clear solution. The reaction mixture was stirred for 12 h. Then, EtOAc (30 mL) was added and the organic phase was washed with 1N HCl. The organic phase was removed. Evaporation of the solvent gave a crude product which was triturated with ether to yield 750 mg (76%) of the title compound.

WORKUP

后处理

  1. customresulting in a clear solution
  2. stirringThe reaction mixture was stirred for 12 h
  3. washthe organic phase was washed with 1N HCl
  4. customThe organic phase was removed
  5. customEvaporation of the solvent
  6. customgave a crude product which
  7. customwas triturated with ether