HRID2356656

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC1(C)NC(=O)N(c2ccc(C#N)c(C(F)(F)F)c2)C1=O

HCID11162285

4-(4,4-Dimethyl-2,5-dioxo-1-imidazolidinyl)-2-(trifluoromethyl)benzonitrile

C13H10F3N3O2

HCID57829308

未命名化合物

PRODUCTS

生成物

结构：CC1(C)C(=O)N(c2ccc(C#N)c(C(F)(F)F)c2)C(=O)N1Cc1cc(Cl)cc(Cl)c1Br

HCID86633595

未命名化合物

收率 55%

PROCEDURE

实验过程

Compound 38.2 was prepared as described for example 6.2, by reacting compound 1.1 with 2-bromo-3,5-dichlorobenzyl bromide. 4-[3-(2-Bromo-3,5-dichlorobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile was obtained in a yield of 55%. 1H NMR: 8.35, d, 1H, 8.25, s, 1H, 8.1, d, 1H, 7.7, s, 1H, 7.65, s, 1H; 4.65, s, 2H, 1.45, s, 6H.