HRID913597
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
Synthesized as described in Example 4 from 4-chloro-2-propyl-1H-indole-5-carbonitrile and 3-bromo-5-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]pyridine: 1H NMR (400 MHz, DMSO-d6) δ 9.03 (d, J=1.3 Hz, 1 H), 8.94 (d, J=2.0 Hz, 1 H), 8.46 (s, 1 H), 7.97 (s, 1 H), 7.81 (d, J=8.5 Hz, 1 H), 7.61 (d, J=8.5 Hz, 1 H), 5.96 (s, 2 H), 2.95-2.87 (m, 2 H), 1.75-1.48 (m, 2 H), 0.93 (t, J=7.3 Hz, 3 H); MS (ES) m/z 457 (M+1).
WORKUP
后处理
- customSynthesized