Mahmoud Arafat, Ehab Khalifa, F. El‐Taweel, S. Ayyad, K. Mohamed
{"title":"一些新的双(吡唑-5-醇)、吡啶酮和含N-(4-氯苯基)-2-(4-甲酰苯氧基)乙酰胺的苯并[f]-硫代铬-2-碳腈衍生物的合成","authors":"Mahmoud Arafat, Ehab Khalifa, F. El‐Taweel, S. Ayyad, K. Mohamed","doi":"10.21608/sjdfs.2022.269870","DOIUrl":null,"url":null,"abstract":"Novel 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1 H -pyrazol-5-ol) derivative 2 was synthesized via interaction of N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ) with diverse available reagent (two mole from 3-methyl-1H-pyrazol-5(4 H )-one). Moreover, One-pot pseudo three-component reaction of hydrazine hydrate, ethyl acetoacetate and aldehydes in ethanole using pipridine at 70°C afforded the corresponding aminopyrazole derivative 3 . on the other hand, cyanoacetamide scaffolds 4a,b was reacted with aromatic aldehyde particularly N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ), to afford arylidenes 5a,b that undergoes cyclization by heating in ethanol containing drops of piperidine as catalyst, and malononitrile afforded the corresponding pyridinone derivatives 6a,b . All freshly synthesized scaffolds were elucidated by considering the data of both elemental and spectral analyses.","PeriodicalId":21655,"journal":{"name":"Scientific Journal for Damietta Faculty of Science","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of some new bis(pyrazol-5-ols), pyridones and benzo-[f]-thiochromene-2-carbonitrile derivatives bearing N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide moiety\",\"authors\":\"Mahmoud Arafat, Ehab Khalifa, F. El‐Taweel, S. Ayyad, K. Mohamed\",\"doi\":\"10.21608/sjdfs.2022.269870\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Novel 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1 H -pyrazol-5-ol) derivative 2 was synthesized via interaction of N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ) with diverse available reagent (two mole from 3-methyl-1H-pyrazol-5(4 H )-one). Moreover, One-pot pseudo three-component reaction of hydrazine hydrate, ethyl acetoacetate and aldehydes in ethanole using pipridine at 70°C afforded the corresponding aminopyrazole derivative 3 . on the other hand, cyanoacetamide scaffolds 4a,b was reacted with aromatic aldehyde particularly N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ), to afford arylidenes 5a,b that undergoes cyclization by heating in ethanol containing drops of piperidine as catalyst, and malononitrile afforded the corresponding pyridinone derivatives 6a,b . All freshly synthesized scaffolds were elucidated by considering the data of both elemental and spectral analyses.\",\"PeriodicalId\":21655,\"journal\":{\"name\":\"Scientific Journal for Damietta Faculty of Science\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Scientific Journal for Damietta Faculty of Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/sjdfs.2022.269870\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scientific Journal for Damietta Faculty of Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/sjdfs.2022.269870","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of some new bis(pyrazol-5-ols), pyridones and benzo-[f]-thiochromene-2-carbonitrile derivatives bearing N-(4-chlorophenyl)-2-(4-formylphenoxy)acetamide moiety
Novel 4,4′-(arylmethylene)-bis(3-methyl-1-phenyl-1 H -pyrazol-5-ol) derivative 2 was synthesized via interaction of N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ) with diverse available reagent (two mole from 3-methyl-1H-pyrazol-5(4 H )-one). Moreover, One-pot pseudo three-component reaction of hydrazine hydrate, ethyl acetoacetate and aldehydes in ethanole using pipridine at 70°C afforded the corresponding aminopyrazole derivative 3 . on the other hand, cyanoacetamide scaffolds 4a,b was reacted with aromatic aldehyde particularly N -(4-chlorophenyl)-2-(4-formylphenoxy)acetamide ( 1 ), to afford arylidenes 5a,b that undergoes cyclization by heating in ethanol containing drops of piperidine as catalyst, and malononitrile afforded the corresponding pyridinone derivatives 6a,b . All freshly synthesized scaffolds were elucidated by considering the data of both elemental and spectral analyses.