HRID2288498

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID14798

Sodium Hydroxide

HNaO

结构：CCOC(=O)CCN(c1ccccc1)S(=O)(=O)c1ccc2c(c1)nc(CNc1ccc(C(=N)N)cc1)n2C.Cl

HCID18412309

未命名化合物

PRODUCTS

生成物

结构：Cn1c(CNc2ccc(C(=N)N)cc2)nc2cc(S(=O)(=O)N(CCC(=O)O)c3ccccc3)ccc21

HCID18412456

未命名化合物

收率 24%

PROCEDURE

实验过程

Prepared analogously to Example 26 from 1-methyl-2-[N-(4-amidinophenyl)-aminomethyl]-benzimidazol-5-yl-sulphonic acid-N-phenyl-N-(2-ethoxycarbonylethyl)-amide-hydrochloride and sodium hydroxide solution. Yield: 24% of theory, Rf value: 0.55 (Reverse-Phase RP-18 silica gel; methanol/5% saline solution=3:2) C25H26N6O4S (506.6) ##EQU112##