HRID1898441
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The title compound was prepared following the procedure described for Example-146 using N-(4-bromophenyl)-2-[(2,6-dichlorophenyl)amino]-7,7-dimethyl-7,8-dihydro-1H-furo[3,2-e]benzimidazole-5-carboxamide (Example-11, 0.100 g), THF and conc. HCl to afford 0.060 g of the desired product. 1HNMR (DMSO-d6): δ 1.56 (s, 6H), 2.20 (s, 2H), 7.51-7.57 (m, 3H), 7.64-7.74 (m, 5H), 9.81 (s, 1H), 12.0-13.0 (br, 3H).
WORKUP
后处理
- customThe title compound was prepared