HRID1064655

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) δ7.7 (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)+;