HRID651829

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(C)C[C@@H](C(=O)NN1C(=O)CN(CCN(C)C)C1=O)[C@H](CCCc1ccccc1)C(=O)NOCc1ccccc1

HCID86757338

未命名化合物

PRODUCTS

生成物

结构：CC(C)C[C@@H](C(=O)NN1C(=O)CN(CCN(C)C)C1=O)[C@H](CCCc1ccccc1)C(=O)NO

HCID86757337

未命名化合物

收率 93.6%

AUXILIARIES

试剂、催化剂与溶剂

催化剂HCID23938

Palladium

溶剂HCID887

Methanol

CH4O

PROCEDURE

实验过程

A solution of 0.061 g of 2(R)-[1(S)-(benzyloxycarbamoyl)-4-phenylbutyl]-N-[3-[2-(dimethylamino)ethyl]-2,5-dioxo-1-imidazolidinyl]-4-methylvaleramide in 10 ml of methanol was hydrogenated in the presence of 0.005 g of 10% palladium-on-carbon for 3 hours. The catalyst was removed by filtration and evaporation gave 0.048 g of 2(R)-[1(S)-(Hydroxycarbamoyl)-4-phenylbutyl]-N-[3-[2-(dimethylamino)ethyl]-2,5-dioxo-1-imidazolidinyl]-4-methylvaleramide in the form of a white solid.

WORKUP

后处理

customThe catalyst was removed by filtration and evaporation