专利号:WO-9410327-A1 优先权日:1992-10-28 标 题 :Enzymatic synthesis of polyaniline 发明人:ZEMEL HAYA; QUINN JOHN F 权利人:ALLIED SIGNAL INC 摘要:This invention relates to a process for the enzymatic synthesis of electrically conductive substituted and unsubstituted polyanilines. Aniline monomer(s), an oxidizing agent, which comprises an enzyme and an electron acceptor, and an acidifying agent are reacted together to form polyanilines.
专利号:US-5243032-A 优先权日:1989-06-22 标题:Preparation of azo pigments with low pcb content by coupling in the presence of olefins 发明人:RIEPER WOLFGANG 权利人:HOECHST AG 摘要:The production which is customary in practice of monoazo compounds based on dichloro- and trichloroanilines or disazo compounds of the chlorinated biphenyl series by conventional coupling methods meets with difficulties in that the resulting pigments are contaminated by traces of polychlorinated biphenyls. n According to the invention, it has now been found that by addition of water-soluble olefins of the type ##STR1## (R =H, alk or Oalk; X =--COOR 1 , --CONHR 2 or --NR 3 COR 4 ) n in the azo coupling, the side reactions which form PCBs can be decidedly suppressed during synthesis of the pigments.
专利号:US-2005080260-A1 优先权日:2003-04-22 标 题 :Preparation of prodrugs for selective drug delivery 发明人:MILLS RANDELL L; WU GUO-ZHANG 摘要:Synthesis of a chemical compound having the formula A-B-C that may serve for applications such as drug delivery where A is a chemiluminescent, moiety, B is a photochromic moiety, and C is a biologically active moiety where A-B-C may serve as a prodrug. Novel synthetic methods of the present invention to form the prodrug comprised the steps of (1) forming a benzophenone, (2) forming a diaryl ethylene, (3) attaching a phthalimide moiety to at least one of the aryl groups of the ethylene to form a phthalimide-ethylene conjugate, (4) condensing two ethylene-phthalimide conjugates to form a phthalimide-pentadiene conjugate, (5) converting the phthalimide to the phthalhydrazide by reaction with hydrazine to form a carrier compound according to the present invention, and (6) reacting the carrier compound with an nucleophilic moiety of the drug to form the corresponding prodrug. Alternatively the carrier can be prepared by using the halo-substituted diaryl ethylene to make the corresponding cationic leuco dye-like compound with known methods. The cationic compound then is protected by reacting with a nucleophile and coupled with the aminophathalimide by palladium-catalyzed amination to form the protected phthalimide-pentadiene conjugate. The latter is refluxed with hydrazine to convert its phthalimide to the phthalhydrazide and acidified to give the carrier. An additional aspect of the present invention relates to the use of these compounds as antiviral agents for the treatment of viral infections such as HIV and as anticancer agents for the treatment of cancers such as bowel, lung, and breast cancer.
专利号:US-4897484-A 优先权日:1986-12-19 标题 :Process for the preparation of substituted pyridines 发明人:WEIS CLAUS D; SUTTER PETER 权利人:CIBA GEIGY CORP 摘要:A process is described for the preparation of compounds of the formula (1) in which R and X are as defined in claim 1. The compounds of the formula (1) are valuable intermediates in the synthesis of triarylmethane dyes and triarylmethanelactones.
专利号:US-10557210-B2 优先权日:2014-02-24 标题 :Direct electrochemical synthesis of doped conductive polymers on metal alloys 发明人:KINLEN PATRICK JOHN; LAWLESS LAWRENCE MICHAEL 权利人:BOEING CO 摘要:This disclosure relates generally to the discovery of improved methods of reducing corrosion on metals and metal alloys without using hexavalent chromium reagents. More particularly, the disclosure relates to preparing corrosion resistant metals using doped conducting polymers such as polyaniline (PANI) on metal alloys such as aluminum alloys.
专利号:WO-2024155469-A1 优先权日:2023-01-19 标 题:One step reaction for the catalytic synthesis of cyclic urea derivatives 发明人:ZHOU HUI 权利人:HUNTSMAN PETROCHEMICAL LLC 摘要:A process for preparing a cyclic urea derivative by reacting an alkylene carbonate and a primary amine in the presence of a metal oxide catalyst to form the cyclic urea derivative.
参考标题:Synthesis, Docking, And Cytotoxic Activities Of Novel 2-Aryl-4-(Arylamino)Quinazolines 作者:Nasrin Rahmannejadi,Soghra Khabnadideh,Issa Yavari |发布日期:2018.11 摘要:Abstracta Synthesis Of Functionalized 2-Aryl-4-(Arylamino)Quinazolines From 4-Chloro-2-Arylquinazolines (Derived From 2-Arylquinazolin-4(3H)-One) And 5-Chloroaniline Derivatives In Dmf Is Described. The Interaction Of 2-Aryl-4-(Arylamino)Quinazolines With Their Biological Target, Human Epithelial Growth Factor Receptor (Egfr), Was Investigated By Molecular Docking. Docking Results Indicated Lower Binding