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HRID1804218

反应详情

EQUATION

反应方程式

HRID 1804218 的结构方程式

REACTANTS

反应物

2
结构：O=C1N[C@H](COC(=O)c2ccccc2)CO1
HCID16213752

未命名化合物

结构：Cc1cnc(N2CCN(C(=O)c3ccc(Br)cc3S(C)(=O)=O)CC2)c(C)c1
HCID58484505

未命名化合物

PRODUCTS

生成物

1
结构：Cc1cnc(N2CCN(C(=O)c3ccc(N4C(=O)OC[C@H]4CO)cc3S(C)(=O)=O)CC2)c(C)c1
HCID67380839

未命名化合物

收率 57.9%

PROCEDURE

实验过程

By reaction and treatment in the same manner as in Example 19 and using (4-bromo-2-methanesulfonylphenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone (1.6 g) described in Preparation Example 61 and benzoic acid (R)-2-oxooxazolidin-4-ylmethyl ester (903 mg), the title compound (1 g) was obtained.

WORKUP

后处理

  1. customBy reaction and treatment in the same manner as in Example 19