{"title":"N-(2-氨基苯甲酰基)苯并三唑介导的 3-酰基-2-烷基(芳基)-4-羟基喹啉和 3-酰氨基-4(3H)喹唑啉酮的合成。","authors":"İlbilge Merve Şenol, Sevtem Gökbulut Satioğlu, İlhami Çelik","doi":"10.55730/1300-0527.3642","DOIUrl":null,"url":null,"abstract":"<p><p>New methods have been developed for the synthesis of the substituted quinolines and quinazolinones derivatives by utilizing <i>N</i>-(2-aminobenzoyl)benzotriazoles under mild reaction conditions. 3-Acyl-2-alkyl(aryl)-4-hydroxyquinolines were obtained in modarete yields by the reaction of <i>N</i>-(2-aminobenzoyl)benzotriazoles and diketones in the presence of <i>tert</i>-BuOK. 3-Acylamino-4(3<i>H</i>) quinazolinones were obtained in good yields via <i>N</i>-(2-aminobenzoyl)benzotriazoles, orthoester and hyrazides in one-pot.</p>","PeriodicalId":23367,"journal":{"name":"Turkish Journal of Chemistry","volume":"48 1","pages":"97-107"},"PeriodicalIF":1.3000,"publicationDate":"2023-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10965190/pdf/","citationCount":"0","resultStr":"{\"title\":\"<i>N</i>-(2-Aminobenzoyl)benzotriazole Mediated Synthesis of 3-Acyl-2-alkyl(aryl)-4-hydroxyquinolines and 3-Acylamino-4(3<i>H</i>) quinazolinones.\",\"authors\":\"İlbilge Merve Şenol, Sevtem Gökbulut Satioğlu, İlhami Çelik\",\"doi\":\"10.55730/1300-0527.3642\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>New methods have been developed for the synthesis of the substituted quinolines and quinazolinones derivatives by utilizing <i>N</i>-(2-aminobenzoyl)benzotriazoles under mild reaction conditions. 3-Acyl-2-alkyl(aryl)-4-hydroxyquinolines were obtained in modarete yields by the reaction of <i>N</i>-(2-aminobenzoyl)benzotriazoles and diketones in the presence of <i>tert</i>-BuOK. 3-Acylamino-4(3<i>H</i>) quinazolinones were obtained in good yields via <i>N</i>-(2-aminobenzoyl)benzotriazoles, orthoester and hyrazides in one-pot.</p>\",\"PeriodicalId\":23367,\"journal\":{\"name\":\"Turkish Journal of Chemistry\",\"volume\":\"48 1\",\"pages\":\"97-107\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-10-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10965190/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Turkish Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.55730/1300-0527.3642\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.55730/1300-0527.3642","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
N-(2-Aminobenzoyl)benzotriazole Mediated Synthesis of 3-Acyl-2-alkyl(aryl)-4-hydroxyquinolines and 3-Acylamino-4(3H) quinazolinones.
New methods have been developed for the synthesis of the substituted quinolines and quinazolinones derivatives by utilizing N-(2-aminobenzoyl)benzotriazoles under mild reaction conditions. 3-Acyl-2-alkyl(aryl)-4-hydroxyquinolines were obtained in modarete yields by the reaction of N-(2-aminobenzoyl)benzotriazoles and diketones in the presence of tert-BuOK. 3-Acylamino-4(3H) quinazolinones were obtained in good yields via N-(2-aminobenzoyl)benzotriazoles, orthoester and hyrazides in one-pot.
期刊介绍:
The Turkish Journal of Chemistry is a bimonthly multidisciplinary journal published by the Scientific and Technological Research Council of Turkey (TÜBİTAK).
The journal is dedicated to dissemination of knowledge in all disciplines of chemistry (organic, inorganic, physical, polymeric, technical, theoretical and analytical chemistry) as well as research at the interface with other sciences especially in chemical engineering where molecular aspects are key to the findings.
The journal accepts English-language original manuscripts and contribution is open to researchers of all nationalities.
The journal publishes refereed original papers, reviews, letters to editor and issues devoted to special fields.
All manuscripts are peer-reviewed and electronic processing ensures accurate reproduction of text and data, plus publication times as short as possible.