期刊
MOLECULAR DIVERSITY
卷 24, 期 1, 页码 241-252出版社
SPRINGER
DOI: 10.1007/s11030-019-09945-4
关键词
1-Aminoalkyl-2-naphthol; Multicomponent reaction (MCRs); Green synthesis; No column chromatography; Solvent-free conditions
类别
资金
- Kerman University of Medical Sciences [21252]
- Jiroft University of Medical Sciences Faculty Research Committee
An efficient, clean and one-pot multicomponent synthesis of divers kind of new functionalized aminoalkyl naphthol and amidoalkyl naphthol derivatives via tandem condensation reaction of 2-naphthol, aromatic aldehydes and 5-methyl-1,3,4-thiadiazol-2-amine/5-aryl-1,3,4-thiadiazol-2-amines urea/acetamide under solvent-free conditions is reported. Following this protocol, it was possible to synthesize novel 1-(((5-methyl-1,3,4-thiadiazol-2-yl)amino)(aryl)methyl)naphthalen-2-ol, 1-(aryl((5-aryl-1,3,4-thiadiazol-2-yl)amino)methyl)naphthalen-2-ol and amidoalkyl naphthol derivatives. This protocol includes some salient features, such as the use of triethylammonium hydrogen sulfate ([Et3NH][HSO4]) ionic liquid as a green, clean and reusable catalyst, no column chromatographic separation, high atom economy, good yields, low cost and finally no need for a complex procedure. [GRAPHICS] .
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