Synthesis of (E)- and (Z)-3(5)-(2-hydroxyphenyl)-4-styrylpyrazoles

被引:17
|
作者
Silva, Vera L. M. [1 ,2 ]
Silva, Artur M. S. [1 ,2 ]
Pinto, Diana C. G. A. [1 ,2 ]
Cavaleiro, Jose A. S. [1 ,2 ]
Elguero, Jose [3 ]
机构
[1] Univ Aveiro, Dept Chem, P-3800 Aveiro, Portugal
[2] Univ Aveiro, QOPNA, P-3800 Aveiro, Portugal
[3] CSIC, Inst Quim Med, E-28006 Madrid, Spain
来源
MONATSHEFTE FUR CHEMIE | 2009年 / 140卷 / 01期
关键词
3-Styrylchromones; 3(5)-(2-Hydroxyphenyl)-4-styrylpyrazoles; Nitrogen heterocycles; NMR spectroscopy; Reaction mechanism; BIOLOGICAL EVALUATION; ULTRAVIOLET STABILIZERS; MOLECULAR CHAPERONE; 4-THIO ANALOGS; INHIBITORS; AGENTS; HSP90; DERIVATIVES; HYDRAZINE; PYRAZOLES;
D O I
10.1007/s00706-008-0002-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient synthesis method for the preparation of a series of new (Z)- and (E)-3(5)-(2-hydroxyphenyl)4-styrylpyrazoles was developed. The reaction of (Z)- and (E)-3-styrylchromones with hydrazine hydrate afforded the corresponding (Z)- and (E)-3(5)-(2-hydroxyphenyl)4-styrylpyrazoles, except for nitro derivatives, where both (Z)- and (E)-4'-nitro-3-styrylchromones afforded (E)-3(5)-(2-hydroxyphenyl)-4-(4-nitrostyryl)pyrazoles. The reaction mechanism for these transformations is discussed and the stereochemistries of all products were established by NMR experiments.
引用
收藏
页码:87 / 95
页数:9
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