Substituted Quinolinones,Part 11:Efficient Synthesis of Different 3-(4-Arylidene and Hetarylidene-5-oxopyrazolin-3-yl) quinolin-2-ones

Mohamed Abass; Elham S.Othman; Akram Hassan

首页> 外文期刊>Synthetic Communications >Substituted Quinolinones,Part 11:Efficient Synthesis of Different 3-(4-Arylidene and Hetarylidene-5-oxopyrazolin-3-yl) quinolin-2-ones

【24h】

Substituted Quinolinones,Part 11:Efficient Synthesis of Different 3-(4-Arylidene and Hetarylidene-5-oxopyrazolin-3-yl) quinolin-2-ones

机译：取代的喹啉酮，第11部分：不同的3-（4-亚芳基和亚芳基5-氧杂唑啉-3-基）喹啉-2-酮的高效合成

获取原文

获取原文并翻译 | 示例

获取外文期刊封面封底 >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Several 3-(4-arylidene and hetarylidene-5-oxopyrazolin-3-yl)quinolin-2-ones 6-26 were synthesized in an efficient methodology utiUzing both pyrazoUnylquinolinone 2 and its chromenylmethylene derivative 10.Compound 2 was derivatized by Knoeve-nagel condensation with different carbonyl compounds.NucleophiUc ring opening-ring closure (RORC) of the compound 10 furnished the desired 4-methylenepyarzolinone bearing novel five-,six-,and seven-membered heterocycles,in good yields.

机译：以高效的方法合成了几个3-（4-亚芳基和亚芳基-5-氧并吡唑啉-3-基）喹啉-2-酮6-26，同时使用了吡唑并基喹啉酮2及其苯并亚甲基衍生物10.化合物2由Knoeve-nagel衍生化合物10的核开环闭环（RORC）以良好的收率提供了所需的带有新的五，六和七元杂环的4-亚甲基吡唑啉酮。

著录项

来源
《Synthetic Communications》 |2007年第6期|共15页
作者
Mohamed Abass; Elham S.Othman; Akram Hassan;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类有机化学;
关键词
heterocyclic synthesis; Knoevenagel condensation; pyrazoUnone; quinoli-none; RORC;

机译：杂环合成;Knoevenagel缩合;吡唑酮;喹诺酮;RORC;

相似文献

外文文献
中文文献
专利

1. Substituted Quinolinones,Part 11:Efficient Synthesis of Different 3-(4-Arylidene and Hetarylidene-5-oxopyrazolin-3-yl) quinolin-2-ones [J] . Mohamed Abass, Elham S.Othman, Akram Hassan Synthetic Communications . 2007,第4a6期

机译：取代的喹啉酮，第11部分：不同的3-（4-亚芳基和亚芳基5-氧杂唑啉-3-基）喹啉-2-酮的高效合成
2. Convenient and Efficient Synthesis of 11-Amino-2,8-substituted-2,3,8,9-tetrahydrobenzo[4,5]thieno[2,3-b]quinolinone Derivatives [J] . Wang Zhong-Xia, Chen Li-Zhuang, Li Bei, Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry . 2015,第6期

机译：便捷合成11-氨基-2,8-取代的2,3,8,9-四氢苯并[4,5]噻吩并[2,3-b]喹啉酮衍生物
3. Synthesis and SAR of 3- and 4-substituted quinolin-2-ones: discovery of mixed 5-HT(1B)/5-HT(2A) receptor antagonists. [J] . McCort G, Hoornaert C, Aletru M, Bioorganic and medicinal chemistry . 2001,第8期

机译：3-和4-取代的喹啉-2-酮的合成和合成孔径雷达：混合的5-HT（1B）/ 5-HT（2A）受体拮抗剂的发现。
4. Methyl(11aS)-1,2,3,5,11,11a-Hexahydro-3,3-dimethyl-1-oxo-6H-imidazo-3',4':1,2pyridin3,4-b-indol-2-Substituted Acetates: Synthesis and Three-Dimensional Quantitative Structure-Activity Relationship Investigation as a Class of Novel Vasodilator [C] . Jiawang Liu, Ming Zhao, Guohui Cui, 第四届国际分子模拟与信息技术应用学术会议（The 4th International Conference of Molecular Simulations and Applied Informatics Technologies）论文集 . 2008

机译：甲基（11aS）-1,2,3,5,11,11a-六氢-3,3-二甲基-1-氧代-6H-咪唑-3'，4'：1,2吡啶3,4- b-吲哚-2-取代的乙酸酯：一类新型血管扩张剂的合成与三维定量构效关系研究
5. The development of sulfamates as latent directed metalation groups. Total synthesis of schumanniophytine. Divergent synthesis of substituted chromone 3- and 8-carboxamides [D] . Macklin, Todd Kristopher 2008

机译：氨基磺酸盐作为潜在的定向金属化基团的发展。舒曼甘草素的全合成。发散合成取代的色酮3-和8-羧酰胺
6. Efficient Solid-Phase Synthesis of 2-Substituted-3-Hydroxy-4(1H)-Quinolinone-7-Carboxamides with Two Diversity Positions [O] . Miroslav Soural, Viktor Krchňák -1

机译：具有两个多样性位置的2-取代的3-羟基-4（1H）-喹啉酮-7-羧酰胺的高效固相合成
7. Efficient and mild synthesis of substituted 2-amino-1,3,4-oxadiazoles mediated by (tosylimino)phenyl-λ3-iodane [O] . Girish Prabhu ., Chilakapathi Madhu ., Vommina V.S. 2014

机译：由（甲苯磺酰亚胺基）苯基-λ3-碘烷介导的取代的2-氨基-1,3,4-恶二唑的有效和温和合成
8. Synthesis, Characterization, and Structural Investigations of 1-amino-3-Substituted- 1,2,3-Triazolium Salts, and a New Route to 1-substituted-1,2,3- triazoles [R] . Kaplan, G. , Drake, G. , Tollison, K. , 2004

机译：1-氨基-3-取代-1,2,3-三唑盐的合成，表征和结构研究，以及1-取代-1,2,3-三唑的新途径

Substituted Quinolinones,Part 11:Efficient Synthesis of Different 3-(4-Arylidene and Hetarylidene-5-oxopyrazolin-3-yl) quinolin-2-ones

摘要

著录项

相似文献

相关主题

期刊订阅