{"title":"二氧化硅-醋酸铵(SiO2-NH4OAc)催化表面合成二氢吡唑[4′,3′:5,6]吡喃[2,3-d]嘧啶-5,7-二酮","authors":"Fatemeh Rigi, H. Shaterian","doi":"10.2478/achi-2018-0004","DOIUrl":null,"url":null,"abstract":"Abstract Silica ammonium acetate (SiO2-NH4OAc) was applied as an inexpensive, practical and heterogeneous catalyst for the preparation of new and known dihydropyrazolo[4',3':5,6]pyrano[2,3-d]pyrimidine-5,7-diones via one-pot four-component reaction of hydrazine hydrate, ethyl acetoacetate aldehydes and barbituric acid/dimethyl barbituric acid under solvent-free conditions. Silica supported ammonium acetate (SiO2-NH4OAc) was prepared according to easy procedure under ambient condition. After completion of the reaction, the catalyst was separated by filtration and reused. So, recycling system, simple work-up, using non-toxic materials, excellent yields and short reaction times makes our research green and convenient for preparation of these classes of organic compounds.","PeriodicalId":6958,"journal":{"name":"Acta Chemica Iasi","volume":"1 1","pages":"45 - 58"},"PeriodicalIF":0.4000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Silica Ammonium Acetate(SiO2-NH4OAc) Catalyzed Facial Synthesis of Dihydropyrazolo[4',3':5,6]Pyrano[2,3-d]Pyrimidine-5,7-Diones\",\"authors\":\"Fatemeh Rigi, H. Shaterian\",\"doi\":\"10.2478/achi-2018-0004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract Silica ammonium acetate (SiO2-NH4OAc) was applied as an inexpensive, practical and heterogeneous catalyst for the preparation of new and known dihydropyrazolo[4',3':5,6]pyrano[2,3-d]pyrimidine-5,7-diones via one-pot four-component reaction of hydrazine hydrate, ethyl acetoacetate aldehydes and barbituric acid/dimethyl barbituric acid under solvent-free conditions. Silica supported ammonium acetate (SiO2-NH4OAc) was prepared according to easy procedure under ambient condition. After completion of the reaction, the catalyst was separated by filtration and reused. So, recycling system, simple work-up, using non-toxic materials, excellent yields and short reaction times makes our research green and convenient for preparation of these classes of organic compounds.\",\"PeriodicalId\":6958,\"journal\":{\"name\":\"Acta Chemica Iasi\",\"volume\":\"1 1\",\"pages\":\"45 - 58\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2018-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Chemica Iasi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2478/achi-2018-0004\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Chemica Iasi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2478/achi-2018-0004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Silica Ammonium Acetate(SiO2-NH4OAc) Catalyzed Facial Synthesis of Dihydropyrazolo[4',3':5,6]Pyrano[2,3-d]Pyrimidine-5,7-Diones
Abstract Silica ammonium acetate (SiO2-NH4OAc) was applied as an inexpensive, practical and heterogeneous catalyst for the preparation of new and known dihydropyrazolo[4',3':5,6]pyrano[2,3-d]pyrimidine-5,7-diones via one-pot four-component reaction of hydrazine hydrate, ethyl acetoacetate aldehydes and barbituric acid/dimethyl barbituric acid under solvent-free conditions. Silica supported ammonium acetate (SiO2-NH4OAc) was prepared according to easy procedure under ambient condition. After completion of the reaction, the catalyst was separated by filtration and reused. So, recycling system, simple work-up, using non-toxic materials, excellent yields and short reaction times makes our research green and convenient for preparation of these classes of organic compounds.