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HRID1417858

反应详情

EQUATION

反应方程式

HRID 1417858 的结构方程式

REACTANTS

反应物

5
结构：NS(=O)(=O)c1ccc(N2CCNCC2)cc1
HCID901897

4-piperazin-1-ylbenzenesulfonamide

C10H15N3O2S

结构：C[C@@H]1CNC[C@H](C)N1
HCID6950261

rel-(2R,6S)-2,6-Dimethylpiperazine

C6H14N2

结构：OCCC1OCCc2ccccc21
HCID14141298

未命名化合物

结构：NS(=O)(=O)c1ccc(N2CCCNCC2)cc1
HCID17792895

未命名化合物

结构：CC1COC(CCCl)c2ccccc21
HCID23288938

未命名化合物

PRODUCTS

生成物

1
结构：NS(=O)(=O)c1ccc(N2CCCN(CC[C@@H]3OCCc4ccccc43)CC2)cc1
HCID53677310

未命名化合物

PROCEDURE

实验过程

Following the general procedure for EXAMPLE 48 and making non-critical variations (-)-2-(isochroman-1-yl)ethanol (LXXIX) and 4-(homopiperazin-1-yl)benzenesulfonamide (IV; prepared from 4-fluorobenzenesulfonamide (III) and homopiperazine (II, Aldrich) by the method of EXAMPLE 47 Step 1) give the title compound, MS (m/z) 415; [α]D -50° (c 0.9996, methylene chloride); IR (mineral oil) 1153, 1595, 1102, 1511 and 1316 cm-1.