Synthesis of Phenanthridines through Palladium-Catalyzed Cascade Reaction of 2-Halo-N-Ms-arylamines with Benzyl Halides/Sulfonates

被引:22
|
作者
Yang, Si-Yi [1 ]
Han, Wen-Yong [1 ]
Zhang, Ding-Lei [1 ]
Zhou, Xiao-Jian [1 ]
Bai, Mei [1 ]
Cui, Bao-Dong [1 ]
Wan, Nan-Wei [1 ]
Yuan, Wei-Cheng [2 ]
Chen, Yong-Zheng [1 ]
机构
[1] Zunyi Med Univ, Gener Drug Res Ctr Guizhou Prov, Sch Pharm, Zunyi 563000, Peoples R China
[2] Chinese Acad Sci, Chengdu Inst Organ Chem, Natl Engn Res Ctr Chiral Drugs, Chengdu 610041, Peoples R China
关键词
Cascade reactions; Nitrogen heterocycles; Nucleophilic substitution; C-H activation; Palladium; BENZIMIDAZOLE-FUSED PHENANTHRIDINES; ONE-POT SYNTHESIS; BIPHENYL ISOCYANIDES; POLYCYCLIC COMPOUNDS; COUPLING REACTIONS; EFFICIENT METHOD; DERIVATIVES; HECK; CYCLIZATION; ARYLATION;
D O I
10.1002/ejoc.201601608
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient palladium-catalyzed nucleophilic substitution/C-H activation/aromatization cascade reaction between readily available 2-halo-N-Ms-arylamines (Ms = methanesulfonyl) and benzyl halides/sulfonates has been described. A wide variety of phenanthridines were synthesized in a one-pot fashion in moderate to high yields (37-86 %). Notably, this method provides a straightforward, facile approach for the synthesis of phenanthridines. The practicality was further substantiated by successfully carrying out a gram-scale preparation.
引用
收藏
页码:996 / 1003
页数:8
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