HRID546587
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
This compound may be prepared as obtained in stage c) of Example 9, but starting with 100 mg of 3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dione obtained in stage b) of Example 9, 2 mL of dimethyl sulphoxide and 60 mg of cyclopentanamine. After chromatography on a column of silica, eluting with a mixture of diethyl ether/ethyl acetate (gradient from 100/0 to 0/100 by volume), 33 mg of 1-(4-{[3-(4-tert-butylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl]methyl}pyridin-2-yl)-3-cyclopentylurea are obtained in the form of a white powder, the characteristics of which are as follows:
WORKUP
后处理
- customThis compound may be prepared
- customas obtained in stage c) of Example 9
- washAfter chromatography on a column of silica, eluting with a mixture of diethyl ether/ethyl acetate (gradient from 100/0 to 0/100 by volume), 33 mg of 1-(4-{[3-(4-tert-butylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl]methyl}pyridin-2-yl)-3-cyclopentylurea
- customare obtained in the form of a white powder