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HRID2374564

反应详情

EQUATION

反应方程式

HRID 2374564 的结构方程式

REACTANTS

反应物

2
结构：CS(=O)(=O)Cl
HCID31297

Methanesulfonyl chloride

CH3ClO2S

结构：CCN1C(=O)C(C)(C)c2cc3[nH]c(-c4n[nH]cc4N)nc3cc21
HCID178462936

未命名化合物

PRODUCTS

生成物

1
结构：CCN1C(=O)C(C)(C)c2cc3nc(-c4n[nH]cc4NS(C)(=O)=O)[nH]c3cc21
HCID178462876

未命名化合物

PROCEDURE

实验过程

N-[3-(5-Ethyl-7,7-dimethyl-6-oxo-3,5,6,7-tetrahydro-imidazo[4,5-f]indol-2-yl)-1H-pyrazol-4-yl]-methanesulfonamide was prepared using 2-(4-Amino-1H-pyrazol-3-yl)-5-ethyl-7,7-dimethyl-5,7-dihydro-1H-imidazo[4,5-f]indol-6-one (100 mg, 0.32 mmol) and Methansulfonylchloride (30 μl, 0.39 mmol). The title compound was obtained as off-white powder (30 mg, 24%).

WORKUP

后处理

  1. customN-[3-(5-Ethyl-7,7-dimethyl-6-oxo-3,5,6,7-tetrahydro-imidazo[4,5-f]indol-2-yl)-1H-pyrazol-4-yl]-methanesulfonamide was prepared