甲氧苯胺置于硫酸,硝酸,溶剂黄146体系中,化学反应生成4-甲氧基-2-硝基乙酰苯胺 参考文献:Diversified Synthesis Of Novel Quinoline And Dibenzo Thiazepine Derivatives Using Known Active Intermediates 标题:Diversified Synthesis Of Novel Quinoline And Dibenzo Thiazepine Derivatives Using Known Active Intermediates 摘要:新型药物的开发以控制常规药物治疗中抗药性感染是当今的需求.通过趋同合成法开发了少量与抗溃疡相关的衍生物.成功合成的衍生物包括二苯并噻嗪啶-吡啶(sln11-Sln15)和苯并咪唑-氢奎宁基衍生物(sln16-Sln20).在最终步骤中采用了微波,超声和常规技术进行耦合.有效的技术被识别为超声技术,主要体现在时间和产率上.报告的化合物通过元素分析和谱学研究(如1H,13C NMR和质谱)进行了结构表征. Doi:10.14233/ajchem.2013.14818
专利号:WO-2004092142-A1 优先权日:2003-04-17 标 题:An improved process for manufacture of substituted benzimidazoles 发明人:VYAS KETAN DHANSUKHAL; SINGH DHARMENDRA; NANDAVADEKAR SANJAY; BHISE SANJAY; JADHAV ATUL; DESAI HEMAL 权利人:IPCA LAB LTD; VYAS KETAN DHANSUKHAL; SINGH DHARMENDRA; NANDAVADEKAR SANJAY; BHISE SANJAY; JADHAV ATUL; DESAI HEMAL 摘要:The present invention relates to a process for the production of benzimidazole derivatives comprising providing an amino acetamido benzene derivative; and condensing and cyclising the aminoacetamido benzene derivative in the presence of a base and in the presence of a cyclising agent under conditions effective to form the benzimidazole derivative. The acetamido benzene derivative has the formula (I) wherein R is OMe or OCHF2. The resulting substituted benzimidazoles are key intermediates in the synthesis of H<+>/K<+>-ATPase irreversible inhibitors, most particularly Omeprazole.
专利号:RU-2030392-C1 优先权日:1991-04-01 标 题 :Method of synthesis of 3-nitro-4-aminoanisole
专利号:CN-113651713-B 优先权日:2021-08-19 标 题:Synthesis method of high-purity 2-nitro-4-acetylaminoanisole
参考标题:3-(Ethoxycarbonyl)-1-(5-Methyl-5-(Nitrosooxy)Hexyl)Pyridin-1-Ium Cation: A Green Alternative To Tert-Butyl Nitrite For Synthesis Of Nitro-Group-Containing Arenes And Drugs At Room Temperature 作者:Palani Natarajan,Renu Chaudhary,Neetu Rani,Sakshi,Paloth Venugopalan |发布日期:2020.2 摘要:Years In The Field Of Green Organic Synthesis. Herein, For The First Time, We Report That A New Task-Specific Nitrite-Based Ionic Liquid Such As 3-(Ethoxycarbonyl)-1-(5-Methyl-5-(Nitrosooxy)Hexyl)Pyridin-1-Ium Bis(Trifluoromethanesulfonyl)Imides (Ts-N-Il) Derived From Biodegradable Ethyl Nicotinate Indeed Acted As An Efficient And Eco-Friendly Reagent For The Synthesis Of Highly Valuable Nitroaromatic
合成参考文献
摘要:U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals., NX#00426 摘要:Schafer, E. W., Jr., and W. A. Bowles Jr. 1985. Acute oral toxicity and repellency of 933 chemicals to house and deer mice. Archives of Environmental Contamination and Toxicology 14:111-129. https://www.aphis.usda.gov/ws/nwrc/chem-effects-db/S_schafer851.pdf