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HRID2212516

反应详情

EQUATION

反应方程式

HRID 2212516 的结构方程式

REACTANTS

反应物

2
结构：O=S(=O)(Cl)c1ccc(Cl)cc1
HCID7398

Benzenesulfonyl chloride, 4-chloro-

C6H4Cl2O2S

结构：C=CCN(C)CCCCCCOc1ccc2c(c1)CCCN2
HCID21966553

Allyl-methyl-[6-(1,2,3,4-tetrahydro-quinolin-6-yloxy)-hexyl]-amine

C19H30N2O

PRODUCTS

生成物

1
结构：C=CCN(C)CCCCCOc1ccc2c(c1)CCCN2S(=O)(=O)c1ccc(Cl)cc1
HCID21966574

未命名化合物

收率 70%

PROCEDURE

实验过程

In analogy to example 3.6, Allyl-methyl-[6-(1,2,3,4-tetrahydro-quinolin-6-yloxy)-hexyl]-amine and 4-chlorobenzene sulfonylchloride were converted to yield Allyl-{5-[1-(4-chloro-benzenesulfonyl)-1,2,3,4-tetrahydro-quinolin-6-yloxy]-pentyl}-methyl-amine (70%) as light yellow oil, MS: 462 (M, 1Cl).