HRID1591454
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
PROCEDURE
实验过程
Prepared from the intermediate obtained in Step A and 2-phenethyl bromide by the procedure described in Example 3, Step A. 1H NMR (200 MHz, CDCl3): 1.37 (s,6H), 1.68 (m,2H), 2.50 (m,4H), 2.7-3.0 (m,2H), 3.70 (m,1H), 4.48 (m,2H), 5.05 (s,2H), 5.66 (s,1H), 6.99 (m,1H), 7.0-7.4 (m,14H). FAB-MS: calculated for C31H35N3O4 513; found 514 (M+H,100%).