HRID1804280

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID73949

2-Oxazolidinone

C3H5NO2

结构：Cc1cnc(N2CCN(C(=O)c3ccc(Cl)cc3N3CCOC3=O)CC2)c(C)c1

HCID54755234

未命名化合物

PRODUCTS

生成物

结构：Cc1cnc(N2CCN(C(=O)c3ccc(N4CCOC4=O)cc3N3CCOC3=O)CC2)c(C)c1

HCID58484732

未命名化合物

收率 17.3%

PROCEDURE

实验过程

By reaction and treatment in the same manner as in Example 201 and using 3-{5-chloro-2-[4-(3,5-dimethylpyridin-2-yl)piperazine-1-carbonyl]phenyl}oxazolidin-2-one (207 mg) described in Preparation Example 120 and oxazolidin-2-one (43.5 mg), the title compound (40.1 mg) was obtained.

WORKUP

后处理

customBy reaction and treatment in the same manner as in Example 201