HRID494761

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID31268

Pyrrolidine

C4H9N

结构：CS(=O)(=O)OCCc1cc2cc(-c3ccc(C#N)cc3)ccc2o1

HCID11393678

2-[5-(4-cyanophenyl)-1-benzofuran-2-yl]ethyl Methanesulfonate

C18H15NO4S

PRODUCTS

生成物

结构：N#Cc1ccc(-c2ccc3oc(CCN4CCCC4)cc3c2)cc1

HCID10087134

4-[2-(2-pyrrolidin-1-ylethyl)-1-benzofuran-5-yl]benzonitrile

C21H20N2O

PROCEDURE

实验过程

The product from Example 1C and pyrrolidine were processed as described in Example 1D to provide the titled compound. 1H NMR (300 MHz, CD3OD) δ 7.7 (m, 5H), 7.50 (d, J=8.7 Hz, 1H), 7.42 (dd, J=8.7, 1.5 Hz, 1H), 6.51 (s, 1H), 3.1 (m 2H), 2.95 (m, 2H), 2.65 (m, 4H), 1.9 (m, 4H); MS (DCI) m/z 317 (M+H)+;