Recyclable Heterogeneous Copper(II)-Catalyzed Oxidative Cyclization of 2-Pyridine Ketone Hydrazones Towards [1,2,3]Triazolo[1,5-a]pyridines

被引:8
|
作者
Jiang, Gan [1 ]
Lin, Yang [1 ]
Cai, Mingzhong [2 ]
Zhao, Hong [1 ]
机构
[1] Guangdong Pharmaceut Univ, Guangdong Cosmet Engn & Technol Res Ctr, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China
来源
SYNTHESIS-STUTTGART | 2019年 / 51卷 / 23期
基金
中国国家自然科学基金;
关键词
copper catalysis; 1; 2; 3]triazolo[1; 5; a ]pyridines; oxidative cyclization; heterogeneous catalysis; N-N coupling; N BOND-FORMATION; SP(3) C-H; CATALYZED DENITROGENATIVE TRANSANNULATION; CROSS-COUPLING REACTIONS; ONE-POT SYNTHESIS; EFFICIENT SYNTHESIS; COORDINATION-COMPOUNDS; MAGNETIC-PROPERTIES; CRYSTAL-STRUCTURE; MOLECULAR-OXYGEN;
D O I
10.1055/s-0037-1610726
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The heterogeneous copper(II)-catalyzed oxidative cyclization of 2-pyridine ketone hydrazones was achieved in ethyl acetate at room temperature in the presence of an MCM-41-anchored bidentate 2-aminoethylamino copper(II) catalyst [MCM-41-2N-Cu(OAc) (2) ], in the presence of air as the oxidant, yielding a wide variety of [1,2,3]triazolo[1,5- a ]pyridines in mostly good to high yields. The present method was also applied to the direct one-pot synthesis of [1,2,3]triazolo[1,5- a ]pyridines from 2-acylpyridine derivatives and hydrazine monohydrate. Importantly, this supported copper(II) catalyst could be conveniently obtained via a simple procedure from easily available and inexpensive reagents, recovered by filtration of the reaction mixture, and reused at least seven times without a significant loss of catalytic activity.
引用
收藏
页码:4487 / 4497
页数:11
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