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HRID1591815

反应详情

EQUATION

反应方程式

HRID 1591815 的结构方程式

REACTANTS

反应物

2
结构：O=S(=O)(Cl)c1ccccc1
HCID7369

Benzenesulfonyl chloride

C6H5ClO2S

结构：Cn1c(C#N)ccc1-c1ccc(N)cc1
HCID16050430

5-(4-Aminophenyl)-1-methyl-1H-pyrrole-2-carbonitrile

C12H11N3

PRODUCTS

生成物

1
结构：Cn1c(C#N)ccc1-c1ccc(NS(=O)(=O)c2ccccc2)cc1
HCID16050906

N-[4-(5-Cyano-1-methyl-1H-pyrrol-2-yl)phenyl]benzenesulfonamide

C18H15N3O2S

PROCEDURE

实验过程

The title compound was prepared according to general procedure for sulfonylation of 5-(4-aminophenyl)-1-methyl-1H-pyrrole-2-carbonitrile using benzenesulfonyl chloride (70 μL, 0.55 mmol) to provide N-[4-(5-cyano-1-methyl-1H-pyrrol-2-yl)phenyl]benzene sulfonamide (0.046 g).

WORKUP

后处理

  1. customThe title compound was prepared