Nickel-Catalyzed Tandem Knoevenagel Condensation and Intramolecular Direct Arylation: Synthesis of Pyrazolo[5,1-a]-isoquinoline Derivatives

被引:18
|
作者
Dhiman, Shiv [1 ]
Nandwana, Nitesh Kumar [1 ]
Saini, Hitesh Kumar [1 ]
Kumar, Dalip [1 ]
Rangan, Krishnan [2 ]
Robertson, Katherine N. [3 ]
Jha, Mukund [4 ]
Kumar, Anil [1 ]
机构
[1] BITS Pilani, Dept Chem, Pilani Campus, Pilani 333031, Rajasthan, India
[2] BITS Pilani, Dept Chem, Hyderabad Campus, Secunderabad 500078, Telangana, India
[3] St Marys Univ, Dept Chem, Halifax, NS B3H 3C3, Canada
[4] Nipissing Univ, Dept Biol & Chem, North Bay, ON P1B 8L7, Canada
关键词
Nickel; tandem reaction; Knoevenagel condensation; C-H functionalization; direct arylation; pyrazolo[5,1-a]isoquinoline; CROSS-COUPLING REACTIONS; C-H ACTIVATION; 3-COMPONENT REACTION; ALKYNE; CONCISE; SULFONOHYDRAZIDE; CYCLOADDITION; HETEROCYCLES; FACILE; ROUTE;
D O I
10.1002/adsc.201701519
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A simple and efficient method for the synthesis of pyrazolo[5,1-a] isoquinoline derivatives has been developed using the nickel-catalyzed reaction of 1-aryl-2-(1H-pyrazol-1-yl) ethan-1-ones and 2-bromo aldehydes. The overall transformation involves tandem Knoevenagel condensation and intramolecular direct arylation via activation of the C5-H bond of the pyrazole ring. A series of 27 drug-like aroyl-substituted pyrazolo[5,1-a] isoquinolines has been synthesized in moderate to good yields.
引用
收藏
页码:1973 / 1983
页数:11
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