HRID1677016

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID81138

Methanamine, N-methoxy-, hydrochloride

C2H8ClNO

HCID6364545

未命名化合物

结构：CCOC(=O)c1c(S(=O)(=O)Cl)c2cc(Cl)ccc2n1S(=O)(=O)c1ccccc1

HCID22401482

未命名化合物

结构：CCOC(=O)c1c(S(=O)(=O)Cl)c2cc(I)ccc2n1S(=O)(=O)c1ccccc1

HCID86601816

未命名化合物

PRODUCTS

生成物

结构：CON(C)S(=O)(=O)c1c(C(N)=O)[nH]c2ccc(I)cc12

HCID11742225

未命名化合物

PROCEDURE

实验过程

Following the procedures described in Steps D and E of Example 1, replacing in Step D ethyl 5-chloro-3-(chlorosulfonyl)-1-(phenylsulfonyl)-1H-indole-2-carboxylate with ethyl 5-iodo-3-(chlorosulfonyl)-1-(phenylsulfonyl)-1H-indole-2-carboxylate, and methylamine hydrochloride with N-methoxy-N-methylamine hydrochloride, the title compound was obtained. Proton NMR for the product was consistent with the titled compound. ESI+ MS: 410.11 [M+H]+.