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HRID331470

反应详情

EQUATION

反应方程式

HRID 331470 的结构方程式

REACTANTS

反应物

2
结构：CS(=O)(=O)c1ccc(C(=O)O)s1
HCID2740497

5-(METHYLSULFONYL)THIOPHENE-2-CARBOXYLIC ACID

C6H6O4S2

结构：Cl.Cl.N[C@H]1CC[C@H](CCN2CCC(c3cccc4c3CCO4)CC2)CC1
HCID178478710

未命名化合物

2 次

PRODUCTS

生成物

1
结构：CS(=O)(=O)c1ccc(C(=O)N[C@H]2CC[C@H](CCN3CCC(c4cccc5c4CCO5)CC3)CC2)s1
HCID178504772

未命名化合物

PROCEDURE

实验过程

The title compound, light yellow solid (107 mg, 83%), MS (ISP) m/z=517.2 [(M+H)+], mp 255° C., was prepared in accordance with the general method of example 1 from trans-4-{2-[4-(2,3-dihydro-benzofuran-4-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine dihydrochloride (intermediate B) (100 mg, 0.25 mmol) and 5-methanesulfonyl-thiophene-2-carboxylic acid.