J. Quiroga, J. Portilla, Silvia Cruz, R. Abonía, B. Insuasty, M. Nogueras, J. Cobo, M. Hursthouse
{"title":"5-氨基- 1h -吡唑与β -三酮反应无溶剂合成融合吡唑[1,5-a]嘧啶","authors":"J. Quiroga, J. Portilla, Silvia Cruz, R. Abonía, B. Insuasty, M. Nogueras, J. Cobo, M. Hursthouse","doi":"10.2174/1874095200801020092","DOIUrl":null,"url":null,"abstract":"The solvent-free reaction between 5-amino-1H-pyrazoles and -triketones (2-acetyldimedone and 2- acetylindandione) leads to the formation of new fused pyrazolo(1,5-a)pyrimidines in good yields. A possible mechanistic route is postulated on the basis of the isolation of the cyclization intermediate. The structures and regiospecificity of the reaction were determined on the basis of nmr measurements and X-ray diffraction.","PeriodicalId":23020,"journal":{"name":"The Open Organic Chemistry Journal","volume":"65 1","pages":"92-99"},"PeriodicalIF":0.0000,"publicationDate":"2008-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Solvent-Free Synthesis of Fused Pyrazolo[1,5-a]pyrimidines by Reaction of 5-Amino-1H-pyrazoles and β -Triketones\",\"authors\":\"J. Quiroga, J. Portilla, Silvia Cruz, R. Abonía, B. Insuasty, M. Nogueras, J. Cobo, M. Hursthouse\",\"doi\":\"10.2174/1874095200801020092\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The solvent-free reaction between 5-amino-1H-pyrazoles and -triketones (2-acetyldimedone and 2- acetylindandione) leads to the formation of new fused pyrazolo(1,5-a)pyrimidines in good yields. A possible mechanistic route is postulated on the basis of the isolation of the cyclization intermediate. The structures and regiospecificity of the reaction were determined on the basis of nmr measurements and X-ray diffraction.\",\"PeriodicalId\":23020,\"journal\":{\"name\":\"The Open Organic Chemistry Journal\",\"volume\":\"65 1\",\"pages\":\"92-99\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-11-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Open Organic Chemistry Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/1874095200801020092\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Open Organic Chemistry Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1874095200801020092","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Solvent-Free Synthesis of Fused Pyrazolo[1,5-a]pyrimidines by Reaction of 5-Amino-1H-pyrazoles and β -Triketones
The solvent-free reaction between 5-amino-1H-pyrazoles and -triketones (2-acetyldimedone and 2- acetylindandione) leads to the formation of new fused pyrazolo(1,5-a)pyrimidines in good yields. A possible mechanistic route is postulated on the basis of the isolation of the cyclization intermediate. The structures and regiospecificity of the reaction were determined on the basis of nmr measurements and X-ray diffraction.