Diversity Synthesis of N-Substituted 2-Amino-1,6-naphthyridine Derivatives under Microwave Irradiation

被引:28
作者
Han, Zheng-Guo [1 ]
Miao, Chun-Bao [2 ]
Shi, Feng [1 ]
Ma, Ning [1 ]
Zhang, Ge [1 ]
Tu, Shu-Jiang [1 ]
机构
[1] Xuzhou Normal Univ, Sch Chem & Chem Engn, Xuzhou 221116, Jiangsu, Peoples R China
[2] Jiangsu Polytech Univ, Sch Chem & Chem Engn, Changzhou 213164, Jiangsu, Peoples R China
来源
JOURNAL OF COMBINATORIAL CHEMISTRY | 2010年 / 12卷 / 01期
基金
美国国家科学基金会;
关键词
TRANSFORMATIONS; EFFICIENT; CHEMISTRY;
D O I
10.1021/cc900030e
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A sequential three-component reaction of 3,5-diarylidenepiperidin-4-one, malononitrile, and amine (such as aromatic amine, cyclopropanamine, and NH4OAc) in acetic acid under microwave irradiation has been developed. In this one-pot reaction, a series of new N-substituted 2-amino-1,6-naphthyridine derivatives were synthesized with excellent yields. This method has the advantages of operational simplicity and increased safety for small-scale fast synthesis of N-aryl 2-amino-1,6-naphthyridines for biomedical screening.
引用
收藏
页码:16 / 19
页数:4
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