HRID1724704

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：N[C@H]1CC[C@@H](c2c[nH]c3ccc(F)cc23)C1

HCID68827169

未命名化合物

结构：CCOc1cccc2c1O[C@@H](COS(=O)(=O)c1ccc(C)cc1)CO2

HCID86593209

未命名化合物

PRODUCTS

生成物

结构：CCOc1cccc2c1O[C@@H](CN[C@H]1CC[C@@H](c3c[nH]c4ccc(F)cc34)C1)CO2

HCID68830010

未命名化合物

收率 64%

PROCEDURE

实验过程

This compound was prepared in the same manner as for Example 1, using [(2R)-8-ethoxy-2,3-dihydro-benzo[1,4]dioxin-2-yl]methyl 4-methylbenzenesulfonate (0.25 g, 0.68 mmol) and cis-3-(5-fluoro-1H-indol-3-yl)-cyclopentylamine (0.3 g, 1.38 mmol), to afford 0.16 g (64%) of the title compound as its hydrochloride salt: MS (ESI) m/z 411 [M+H]+.

WORKUP

后处理

customThis compound was prepared in the same manner as for Example 1