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HRID258621

反应详情

EQUATION

反应方程式

HRID 258621 的结构方程式

REACTANTS

反应物

3
结构：CCOC(=O)CCCCCCN(CC#CC1(OC(C)=O)CCCCC1)S(C)(=O)=O
HCID20327718

未命名化合物

结构：CCCCC[C@H](C#CCBr)OC(C)=O
HCID22793816

未命名化合物

结构：CC(=O)OC1(C#CCBr)CCCCC1
HCID23339581

未命名化合物

PRODUCTS

生成物

1
结构：CS(=O)(=O)N(CCCCCCC(=O)O)CCCC1(O)CCCCC1
HCID20327665

未命名化合物

PROCEDURE

实验过程

The synthesis of this compound is carried out as described in Example 3 except that, in Step A, the 1-bromo- 4(R)-acetoxy-2-nonyne is replaced by an equimolar amount of 1-acetoxy-1-(3-bromo-1-propynyl)cyclohexane (Example U). The product of Step A is thus ethyl 7-{N-[3-(1-acetoxycyclohexyl)-2-propynyl]methanesulfonamido}heptanoate.

WORKUP

后处理

  1. customThe synthesis of this compound