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7-氨基-4,6-二硝基苯并氧化呋咱的合成反应研究
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作者 张玮 张坤玲 +2 位作者 李瑞珍 吕连营 王建龙 《石家庄职业技术学院学报》 2012年第4期9-12,共4页
分析和讨论了以3-氯苯胺为原料,经酰化、硝化、叠氮化热解脱氮及水解合成7-氨基-4,6-二硝基苯并氧化呋咱反应的机理及反应条件.此反应收率高,条件温和.
关键词 7-氨基-4 6-二硝基苯并氧化呋咱 酰化 硝化 叠氮化 反应
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Synthesis and Crystal Structure of Ethyl 2-(6-(1,3-Dioxo-4,5,6,7-tetrahydro-1H-isoindol-2(3H)-yl)-7-fluoro-3-oxo-2H-benzo[b][1,4]oxazin-4(3H)-yl) Butanoate
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作者 吴道新 罗斐贤 +4 位作者 莫洪波 王晓光 任叶果 SIMPSON Jim 黄明智 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2009年第5期585-589,共5页
The title compound ethyl 2-(6-(1,3-dioxo-4,5,6,7-tetrahydro-lH-isoindol-2(3H)- yl)-7-fluoro-3-oxo-2H-benzo[b][1,4]oxazin-4(3H)-yl) butanoate 3 was synthesized by the reaction of ethyl 2-(6-amino-7-fluoro-3-ox... The title compound ethyl 2-(6-(1,3-dioxo-4,5,6,7-tetrahydro-lH-isoindol-2(3H)- yl)-7-fluoro-3-oxo-2H-benzo[b][1,4]oxazin-4(3H)-yl) butanoate 3 was synthesized by the reaction of ethyl 2-(6-amino-7-fluoro-3-oxo-2H-benzo[b][1,4]oxazin-4(3H)-yl) butanoate with 4,5,6,7- tetraydrophthalic anhydride, and its structure was determined by X-ray single-crystal diffraction. The crystal belongs to the monoclinic system, space group P2 1/n with a = 9.3469(2), b = 16.7715(5), c = 13.7153(4) A, β= 104.9680(10)°, μ = 0.107 mm^-1, Mr = 430.42, V= 2077.08(10) ,A3, Z= 4, Dc = 1.376 g/cm3, F(000) = 904, T= 296(2) K, R = 0.0508 and wR = 0.1478. 展开更多
关键词 synthesis crystal structure ethyl 2-(6-amino-7-fluoro-3-oxo-2H-benzo[b][1 4]oxazin-4(3H)-yl) butanoate herbicidal protox inhibitors
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A Facile Synthesis of 9,10-Dimethoxybenzo[6,7]- ox-epino[3,4-<i>b</i>]quinolin-13(6<i>H</i>)-one and Its Derivatives
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作者 Dingqiao Yang Xiuli Liang +1 位作者 Xiongjun Zuo Yuhua Long 《International Journal of Organic Chemistry》 2013年第2期119-124,共6页
A concise and efficient method for the synthesis of novel 9,10-imethoxybenzo[6,7]oxepino[3,4-b]quinolin13(6H)-one and its derivatives 7a-p has been developed via the intramolecular Friedel-Crafts acylation reactions o... A concise and efficient method for the synthesis of novel 9,10-imethoxybenzo[6,7]oxepino[3,4-b]quinolin13(6H)-one and its derivatives 7a-p has been developed via the intramolecular Friedel-Crafts acylation reactions of 6,7-dimethoxy-2-(phenoxymethyl)quinoline-3-carboxylic acids 6a-p with polyphosphoric acid (PPA) as catalyst and solvent under mild conditions. The key intermediates 6a-p were prepared through the in situ formation of ethyl 6,7-dimethoxy-2-(phenoxymethyl)quinoline-3-carboxylates 5a-p followed by hydrolysis with aqueous ethanolic sodium hydroxide solution. The novel synthetic method has the advantages of good yields, easy work-up, and environmentally friendly character, which may provide a novel highly efficient process for making quinoline and related azaheterocycle libraries. 展开更多
关键词 The Intramolecular Friedel-Crafts acylation Reaction: 9 10-Dimethoxybenzo [6 7]oxepino[3 4-b]quinolin-13(6H)-one and Its DERIVATIVES 6 7-Dimethoxy-2-(phenoxymethyl)quinoline-3-carboxylic Acid: Ethyl 7-dimethoxy-2-(phenoxymethyl)quinoline-3-carboxylate: PPA
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An efficient regioselective sonochemical synthesis of novel 4-aryl-3-methyl-4,5-dihydro-1H-pyrazolo[3,4-b]pyridin-6(7H)-ones 被引量:1
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作者 Abbas Azimi Roshan Manouchehr Mamaghani +1 位作者 Nosrat Ollah Mahmoodi Farhad Shirini 《Chinese Chemical Letters》 SCIE CAS CSCD 2012年第4期399-402,共4页
An efficient ultrasound-assisted preparation of a series of novel 4-aryl-3-methyl-4,5-dihydro-l//-pyrazolo[34-b]pyridin-6(7H)ones via the reaction of 5-amino-3-methyl-1H-pyrazole,Meldrum's acid and various arylalde... An efficient ultrasound-assisted preparation of a series of novel 4-aryl-3-methyl-4,5-dihydro-l//-pyrazolo[34-b]pyridin-6(7H)ones via the reaction of 5-amino-3-methyl-1H-pyrazole,Meldrum's acid and various arylaldehydes using one-pot three-component approach is described.This rapid method produced the products in short reaction times(3-4 min) and excellent yields(87-95%). 展开更多
关键词 Pyrazolo[3 4-b]pyridin-67H)-one Meldrum's acid 5-amino-3-methylpyrazole One-pot Ultrasonic irradiation Three-component REGIOSELECTIVE
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Improved microwave-assisted catalyst-free synthesis of9-aryl-5,9-dihydropyrimido[4,5-d][1,2,4]triazolo[1,5-a]pyrimidine-6,8(4H,7H)-dione derivatives
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作者 Mahnaz Farahi Bahador Karami Zohreh Banaki 《Chinese Chemical Letters》 SCIE CAS CSCD 2015年第9期1065-1067,共3页
Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8(4H,7H)-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-... Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8(4H,7H)-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-1,2,4-triazoles,aromatic aldehydes and barbituric acids under solvent- and catalyst-free conditions.This operationally simple procedure is less laborious and provides a better scope than previously reported procedures. 展开更多
关键词 9-Aryl-5 9-dihydropyrimido[4 5-d] [ 1 2 4]triazolo[1 5-a]pyrimidine- 6 8(4H 7H)-diones Barbituric acids 3-amino- 1 H- 1 2 4-triazoles Aryl aldehydes Microwave-assisted synthesis
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新型含氟酰胺化羟甲香豆素衍生物的合成及生物活性 被引量:8
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作者 乔丽丽 魏艳 郝双红 《有机化学》 SCIE CAS CSCD 北大核心 2018年第2期509-518,共10页
以羟甲香豆素为先导,利用活性亚结构拼接原理,通过引入三氟甲基及酰胺基,设计、合成了系列新型含氟酰胺化羟甲香豆素衍生物,其结构用~1H NMR、^(13)C NMR、HRMS表征,N-正丁酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f1)及N-对... 以羟甲香豆素为先导,利用活性亚结构拼接原理,通过引入三氟甲基及酰胺基,设计、合成了系列新型含氟酰胺化羟甲香豆素衍生物,其结构用~1H NMR、^(13)C NMR、HRMS表征,N-正丁酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f1)及N-对甲苯甲酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f9)的结构经X射线单晶衍射进一步确证.除草活性初筛表明,化合物f1、N-苯乙酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f13)、N-甲基丙烯酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f5)、N-环丙甲酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f7)及N-(6-氯烟酰基)-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f20)对马唐幼茎的生长具有强烈抑制作用,f9、f7及N-(萘-2-甲酰基)-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f17)对灰藜幼茎生长具有良好抑制作用,其抑制率高于对照药剂乙草胺.作物安全评价结果表明,化合物f1、f9及f13对双子叶作物白菜及油菜比较安全,对单子叶作物小麦及高粱比较敏感.抑菌活性评价表明,N-间溴苯甲酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆(f12)、f7及f9对番茄灰霉病菌具有较好抑制作用,N-氢化肉桂酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素(f14)对苹果腐烂病菌具有较好抑制作用. 展开更多
关键词 N-酰基-N-间氟苄基-6-氨基-7-甲氧基-4-三氟甲基香豆素衍生物 合成 除草活性 抑菌活性
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