通过迈克尔加成反应设计和合成新的[1,3]噻唑并[4,5-d]嘧啶融合杂环

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
A. N. Ayyash, H. A. K. Al-Hadithe, N. A. H. Al-Mohammadi
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引用次数: 0

摘要

- 通过一种简单、高效、方便的方法,合成了一系列新的融合杂环 [1,3]噻唑并[4,5-d]嘧啶,4a-4c,产量良好。作为起始材料,硫代氨基脲与 4-N,N-二甲基苯甲醛缩合生成硫代氨基脲 1,再与巯基乙酸环化生成 4-噻唑烷酮 2。此外,通过 4-噻唑烷酮与各种醛的融合,制备出了查耳酮 3a-3c。最后,通过 4-噻唑烷酮与硫脲的迈克尔加成反应,制备出了有名称的化合物 4a-4c。所有新化合物的化学结构都是通过元素分析和光谱分析推导出来的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design and Synthesis of New Fused-Heterocycles of [1,3]Thiazolo[4,5-d]pyrimidines via Michael Addition Reaction

Design and Synthesis of New Fused-Heterocycles of [1,3]Thiazolo[4,5-d]pyrimidines via Michael Addition Reaction

– In a simple and efficient convenient method, a series of new fused heterocycles of [1,3]thiazolo[4,5-d]­pyrimidines, 4a–4c were synthesized with good yields. As starting materials, thiosemicarbazide was condensed with 4-N,N-dimethylbenzaldehyde to afford thiosemicarbazone 1 which further cyclized with mercaptoacetic acid to produce 4-thiazolidinone 2. Furthermore, chalcones 3a–3c was prepared through fusion of 4-thiazolidinones with various aldehydes. Finally, the entitled compounds 4a–4c has been obtained via Michael addition reaction of 4-thiazolidinones with thiourea. The chemical structures for all new compounds were deduced from their elemental and spectral analysis.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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