A. N. Ayyash, H. A. K. Al-Hadithe, N. A. H. Al-Mohammadi
{"title":"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","authors":"A. N. Ayyash, H. A. K. Al-Hadithe, N. A. H. Al-Mohammadi","doi":"10.1134/S1070428024070157","DOIUrl":null,"url":null,"abstract":"<p>– In a simple and efficient convenient method, a series of new fused heterocycles of [1,3]thiazolo[4,5-<i>d</i>]pyrimidines, <b>4a–4c</b> were synthesized with good yields. As starting materials, thiosemicarbazide was condensed with 4-<i>N</i>,<i>N</i>-dimethylbenzaldehyde to afford thiosemicarbazone <b>1</b> which further cyclized with mercaptoacetic acid to produce 4-thiazolidinone <b>2</b>. Furthermore, chalcones <b>3a–3c</b> was prepared through fusion of 4-thiazolidinones with various aldehydes. Finally, the entitled compounds <b>4a–4c</b> 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.</p>","PeriodicalId":766,"journal":{"name":"Russian Journal of Organic Chemistry","volume":null,"pages":null},"PeriodicalIF":0.8000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Design and Synthesis of New Fused-Heterocycles of [1,3]Thiazolo[4,5-d]pyrimidines via Michael Addition Reaction\",\"authors\":\"A. N. Ayyash, H. A. K. Al-Hadithe, N. A. H. Al-Mohammadi\",\"doi\":\"10.1134/S1070428024070157\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>– In a simple and efficient convenient method, a series of new fused heterocycles of [1,3]thiazolo[4,5-<i>d</i>]pyrimidines, <b>4a–4c</b> were synthesized with good yields. As starting materials, thiosemicarbazide was condensed with 4-<i>N</i>,<i>N</i>-dimethylbenzaldehyde to afford thiosemicarbazone <b>1</b> which further cyclized with mercaptoacetic acid to produce 4-thiazolidinone <b>2</b>. Furthermore, chalcones <b>3a–3c</b> was prepared through fusion of 4-thiazolidinones with various aldehydes. Finally, the entitled compounds <b>4a–4c</b> 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.</p>\",\"PeriodicalId\":766,\"journal\":{\"name\":\"Russian Journal of Organic Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2024-10-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1070428024070157\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1070428024070157","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
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.
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.