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HRID1804155

反应详情

EQUATION

反应方程式

HRID 1804155 的结构方程式

REACTANTS

反应物

2
结构：CC(C)(C)[C@@H]1COC(=O)N1
HCID2734860

(4R)-4-tert-Butyl-1,3-oxazolidin-2-one

C7H13NO2

结构：Cc1ccc(N2CCN(C(=O)c3ccc(Br)cc3S(C)(=O)=O)CC2)c(C)c1
HCID58484856

未命名化合物

PRODUCTS

生成物

1
结构：Cc1ccc(N2CCN(C(=O)c3ccc(N4C(=O)OCC4C(C)(C)C)cc3S(C)(=O)=O)CC2)c(C)c1
HCID67381400

未命名化合物

收率 0.9%

PROCEDURE

实验过程

By reaction and treatment in the same manner as in Example 1 and using (4-bromo-2-methanesulfonylphenyl)[4-(2,4-dimethylphenyl)piperazin-1-yl]methanone (903 mg) described in Preparation Example 9 and (R)-4-tert-butyloxazolidin-2-one (286 mg), the title compound (9 mg) was obtained.

WORKUP

后处理

  1. customBy reaction and treatment in the same manner as in Example 1