HRID1409864

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID219302

Oxane-4-carboxylic acid

C6H10O3

结构：Cl.Cl.N[C@H]1CC[C@H](CCN2CCCCC2c2coc3cccc-3c2)CC1

HCID178478713

未命名化合物

2 次

PRODUCTS

生成物

结构：O=C(N[C@H]1CC[C@H](CCN2CCCCC2c2coc3cccc-3c2)CC1)C1CCOCC1

HCID178523658

未命名化合物

PROCEDURE

实验过程

The title compound, white solid (66 mg, 60%), MS (ISP) m/z=439.4 [(M+H)+], mp 175° C., was prepared in accordance with the general method of example 1 from trans-4-[2-(4-benzofuran-3-yl-piperidin-1-yl)-ethyl]-cyclohexylamine dihydrochloride (intermediate A) (100 mg, 0.25 mmol) and tetrahydro-pyran-4-carboxylic acid.