{"title":"蛋壳粉介导的铜催化剂:基于生物废料的喹唑啉-4(3H)-酮和丙炔胺合成催化方法","authors":"Nilakshi Dutta , Kaberi Hazarika , Roktopol Hazarika , Bulan B. Boruah , Surajit Konwer , Bipul Sarma , Diganta Sarma","doi":"10.1016/j.tgchem.2024.100055","DOIUrl":null,"url":null,"abstract":"<div><p>A novel and efficient approach for a tandem oxidative synthesis of quinazolin-4(<em>3H</em>)-one from 2-aminobenzonitrile and benzyl alcohol has been unveiled via Cu<sub>2</sub>(CO<sub>3</sub>)(OH)<sub>2</sub>. Herein CuSO<sub>4.</sub>5H<sub>2</sub>O accompanied by egg shell powder is used for the easy preparation of Cu<sub>2</sub>(CO<sub>3</sub>)(OH)<sub>2</sub>. The reported method portrays a wide range of substrate scope with good to excellent yield and the given reaction proceed at room temperature within 12 h. Single crystal of one of the synthesized quinazolin-4(<em>3H</em>)-ones was analysed through single crystal X-ray diffraction (SC-XRD). Some of the compounds reported here are also known to possess various pharmaceutical activities. Eventually the newly prepared catalyst was applied for propargylamine synthesis via a multi component reaction. Perceiving all the advantages, present protocol is conceivably considered as clean, cost-effective and sustainable over reported procedures used for synthesis of quinazolin-4(<em>3H</em>)-ones and propargyl amines.</p></div>","PeriodicalId":101215,"journal":{"name":"Tetrahedron Green Chem","volume":"4 ","pages":"Article 100055"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2773223124000207/pdfft?md5=c9c788110c513235d50753ee01d75177&pid=1-s2.0-S2773223124000207-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Egg shell powder mediated Cu catalyst: A biowaste based catalytic approach for the synthesis of quinazolin-4(3H)-ones and propargyl amines\",\"authors\":\"Nilakshi Dutta , Kaberi Hazarika , Roktopol Hazarika , Bulan B. Boruah , Surajit Konwer , Bipul Sarma , Diganta Sarma\",\"doi\":\"10.1016/j.tgchem.2024.100055\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A novel and efficient approach for a tandem oxidative synthesis of quinazolin-4(<em>3H</em>)-one from 2-aminobenzonitrile and benzyl alcohol has been unveiled via Cu<sub>2</sub>(CO<sub>3</sub>)(OH)<sub>2</sub>. Herein CuSO<sub>4.</sub>5H<sub>2</sub>O accompanied by egg shell powder is used for the easy preparation of Cu<sub>2</sub>(CO<sub>3</sub>)(OH)<sub>2</sub>. The reported method portrays a wide range of substrate scope with good to excellent yield and the given reaction proceed at room temperature within 12 h. Single crystal of one of the synthesized quinazolin-4(<em>3H</em>)-ones was analysed through single crystal X-ray diffraction (SC-XRD). Some of the compounds reported here are also known to possess various pharmaceutical activities. Eventually the newly prepared catalyst was applied for propargylamine synthesis via a multi component reaction. Perceiving all the advantages, present protocol is conceivably considered as clean, cost-effective and sustainable over reported procedures used for synthesis of quinazolin-4(<em>3H</em>)-ones and propargyl amines.</p></div>\",\"PeriodicalId\":101215,\"journal\":{\"name\":\"Tetrahedron Green Chem\",\"volume\":\"4 \",\"pages\":\"Article 100055\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2773223124000207/pdfft?md5=c9c788110c513235d50753ee01d75177&pid=1-s2.0-S2773223124000207-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron Green Chem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2773223124000207\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron Green Chem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773223124000207","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
通过 Cu2(CO3)(OH)2,一种以 2-氨基苯甲腈和苯甲醇为原料串联氧化合成喹唑啉-4(3H)-酮的新型高效方法已经问世。在这里,CuSO4.5H2O 和蛋壳粉一起被用于轻松制备 Cu2(CO3)(OH)2。通过单晶 X 射线衍射 (SC-XRD) 分析了合成的一种喹唑啉-4(3H)-酮的单晶。报告中的一些化合物还具有多种药物活性。最终,新制备的催化剂被用于通过多组分反应合成丙炔胺。考虑到所有这些优点,可以认为本方案比已报道的用于合成喹唑啉-4(3H)-酮和丙炔胺的程序更加清洁、经济和可持续。
Egg shell powder mediated Cu catalyst: A biowaste based catalytic approach for the synthesis of quinazolin-4(3H)-ones and propargyl amines
A novel and efficient approach for a tandem oxidative synthesis of quinazolin-4(3H)-one from 2-aminobenzonitrile and benzyl alcohol has been unveiled via Cu2(CO3)(OH)2. Herein CuSO4.5H2O accompanied by egg shell powder is used for the easy preparation of Cu2(CO3)(OH)2. The reported method portrays a wide range of substrate scope with good to excellent yield and the given reaction proceed at room temperature within 12 h. Single crystal of one of the synthesized quinazolin-4(3H)-ones was analysed through single crystal X-ray diffraction (SC-XRD). Some of the compounds reported here are also known to possess various pharmaceutical activities. Eventually the newly prepared catalyst was applied for propargylamine synthesis via a multi component reaction. Perceiving all the advantages, present protocol is conceivably considered as clean, cost-effective and sustainable over reported procedures used for synthesis of quinazolin-4(3H)-ones and propargyl amines.