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HRID258615

反应详情

EQUATION

反应方程式

HRID 258615 的结构方程式

REACTANTS

反应物

3
结构：CCCCCC(CCCCl)OC(C)=O
HCID13104716

未命名化合物

结构：CCCCC(C)(C)C(CCCN(CCCCCCC(=O)OCC)S(C)(=O)=O)OC(C)=O
HCID20327680

未命名化合物

结构：CCCCC(C)(C)C(CCCCl)OC(C)=O
HCID20386107

未命名化合物

PRODUCTS

生成物

1
结构：CCCCC[C@@H](O)C#CCN(CCCCCCC(=O)O)S(C)(=O)=O
HCID22798404

未命名化合物

PROCEDURE

实验过程

The synthesis of this compound is carried out as described in Example 1 except that, in Step A, the 1-chloro-4-acetoxynonane is replaced by an equimolar amount of 1-chloro-4-acetoxy-5,5-dimethylnonane (Example G). The product of Step A is thus ethyl 7-[N-(4-acetoxy-5,5-dimethylnonyl)methanesulfonamido]heptanoate. The subsequent step yields 7-[N-(4-hydroxy-5,5-dimethylnonyl)methanesulfonamido]heptanoic acid (B).

WORKUP

后处理

  1. customThe synthesis of this compound