合成目标产物 Phensuximide 主要起始原料 N-Methylmaleimide And Phenylboronic Acid
398130-26-2 = 86-34-0 反应条件:1.1 Reagents: Acetic Acid,Zinc Solvents: Acetic Acid 标题:Synthesis Of Methylthiomaleimides For The Preparation Of Pyridazines And Related Compounds 作者:Tominaga,Yoshinori; Et Al 参考文献:Journal Of Heterocyclic Chemistry 日期:2002 卷标:39(3) 页码:571-591]
398130-26-2 = 86-34-0 反应条件:1.1 Reagents: Zinc Solvents: Acetic Acid 标题:Synthesis Of 3-Methylthio-4-Aryl-3-Pyrroline-2,5-Diones And 3-Arylpyrrolidine-2,5-Diones By Reaction Of Nitroketene Dithioacetal With Arylacetonitriles 作者:Shigemitsu,Yasuhiro; Et Al 参考文献:Heterocycles 日期:2001 卷标:55(12) 页码:2257-2260]
635-51-8 = 86-34-0 [标题:Reaction Conditions 标题:Anticonvulsants. I. N-R-α-R1-α-Phenylsuccinimides 作者:Miller,C. A.; Et Al 参考文献:Journal Of The American Chemical Society 日期:1951 卷标:73 页码:4895-8]
930-88-1 + 98-80-6 = 86-34-0 反应条件:1.1 Catalysts: 4,4′-Bipyridine,Palladium Diacetate Solvents: Acetic Acid,Tetrahydrofuran,Water; 24 H,80 °C1.2 Reagents: Sodium Bicarbonate Solvents: Water; Neutralized 标题:A Unified Strategy For The Synthesis Of Difluoromethyl- And Vinylfluoride-Containing Scaffolds 作者:Duchemin,Nicolas; Et Al 参考文献:Organic Letters 日期:2019 卷标:21(20) 页码:8205-8210]
930-88-1 + 65-85-0 = 86-34-0 反应条件:1.1 Catalysts: [(1,2,3,4,5,6-η)-1-Methyl-4-(1-Methylethyl)Benzene](2,4,6-Trimethylbenzoato-Ko)(... Solvents: 1,2-Dichloroethane; 24 H,110 °C 标题:Mild Decarboxylative C-H Alkylation: Computational Insights For Solvent-Robust Ruthenium(Ii) Domino Manifold 作者:Kumar,N. Y. Phani; Et Al 参考文献:Chemistry - A European Journal 日期:2017 卷标:23(69) 页码:17449-17453]
22903-00-0 = 86-34-0 反应条件:1.1 Reagents: Potassium Carbonate Solvents: Acetone2.1 Reagents: Zinc Solvents: Acetic Acid 标题:Synthesis Of 3-Methylthio-4-Aryl-3-Pyrroline-2,5-Diones And 3-Arylpyrrolidine-2,5-Diones By Reaction Of Nitroketene Dithioacetal With Arylacetonitriles 作者:Shigemitsu,Yasuhiro; Et Al 参考文献:Heterocycles 日期:2001 卷标:55(12) 页码:2257-2260]
= 86-34-0 反应条件:1.1 Reagents: Sodium Nitrite,Tetrafluoroboric Acid Solvents: Water; 20 Min,0 °C; 3 H,0 °C2.1 Reagents: Sodium Acetate Catalysts: Titanium Chloride (Ticl3) Solvents: Acetone; 0 °C2.2 1 H,0 °C; 0 °C -> 25 °C; 6 H,25 °C 标题:Selective And Tunable Synthesis Of 3-Arylsuccinimides And 3-Arylmaleimides From Arenediazonium Tetrafluoroborates And Maleimides 作者:Yang,Zhen-Hua; Et Al 参考文献:Rsc Advances 日期:2016 卷标:6(28) 页码:23438-23447]
49601-28-7 = 86-34-0 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Methanol,Water2.1 Reagents: Potassium Carbonate Solvents: Acetone3.1 Reagents: Zinc Solvents: Acetic Acid 标题:Synthesis Of 3-Methylthio-4-Aryl-3-Pyrroline-2,5-Diones And 3-Arylpyrrolidine-2,5-Diones By Reaction Of Nitroketene Dithioacetal With Arylacetonitriles 作者:Shigemitsu,Yasuhiro; Et Al 参考文献:Heterocycles 日期:2001 卷标:55(12) 页码:2257-2260]
13623-94-4 = 86-34-0 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Dimethyl Sulfoxide1.2 Reagents: Methanol Solvents: Methanol2.1 Reagents: Hydrochloric Acid Solvents: Methanol,Water3.1 Reagents: Potassium Carbonate Solvents: Acetone4.1 Reagents: Zinc Solvents: Acetic Acid 标题:Synthesis Of 3-Methylthio-4-Aryl-3-Pyrroline-2,5-Diones And 3-Arylpyrrolidine-2,5-Diones By Reaction Of Nitroketene Dithioacetal With Arylacetonitriles 作者:Shigemitsu,Yasuhiro; Et Al 参考文献:Heterocycles 日期:2001 卷标:55(12) 页码:2257-2260]
3464-18-4 = 86-34-0 反应条件:1.1 Reagents: Potassium Carbonate Solvents: Acetone; Overnight,Reflux 标题:Light-Induced Divergent Cyanation Of Alkynes Enabled By Phosphorus Radicals 作者:Zhang,Yanyan; Et Al 参考文献:Angewandte Chemie 日期:2022 卷标:61(50)]
635-51-8 = 86-34-0 反应条件:1.1 Catalysts: Niobium Oxide (Nb2O3) Solvents: Hexane,Water; Rt -> Reflux; 30 H,Reflux 标题:Versatile And Sustainable Synthesis Of Cyclic Imides From Dicarboxylic Acids And Amines By Nb2O5 As A Base-Tolerant Heterogeneous Lewis Acid Catalyst 作者:Ali,Ayub Md.; Et Al 参考文献:Chemistry - A European Journal 日期:2014 卷标:20(44) 页码:14256-14260]
930-88-1 + 98-80-6 = 86-34-0 反应条件:1.1 Catalysts: 4,4′-Bipyridine,Palladium Diacetate Solvents: Acetic Acid,Tetrahydrofuran,Water; 24 H,80 °C1.2 Reagents: Sodium Bicarbonate Solvents: Water; Neutralized 标题:Sequential C-Selective Difluoromethylation/pd-Catalyzed Decarboxylative Protonation: An Efficient Access To Tertiary Difluoromethylated Scaffolds 作者:Duchemin,Nicolas; Et Al 参考文献:Chemrxiv 日期:2019 卷标:1 页码:1-8]
930-88-1 + 14874-70-5 + 2684-02-8 = 86-34-0 反应条件:1.1 Reagents: Sodium Acetate Catalysts: Titanium Chloride (Ticl3) Solvents: Acetone; 0 °C1.2 1 H,0 °C; 0 °C -> 25 °C; 6 H,25 °C 标题:Selective And Tunable Synthesis Of 3-Arylsuccinimides And 3-Arylmaleimides From Arenediazonium Tetrafluoroborates And Maleimides 作者:Yang,Zhen-Hua; Et Al 参考文献:Rsc Advances 日期:2016 卷标:6(28) 页码:23438-23447]
930-88-1 + 853955-69-8 = 86-34-0 反应条件:1.1 Catalysts: Bis[(1,2,5,6-η)-1,5-Cyclooctadiene]Di-μ-Hydroxydirhodium Solvents: Tetrahydrofuran; 4 H,35 °C 标题:Organo[2-(Hydroxymethyl)Phenyl]Dimethylsilanes As Mild And Reproducible Agents For Rhodium-Catalyzed 1,4-Addition Reactions 作者:Nakao,Yoshiaki; Et Al 参考文献:Journal Of The American Chemical Society 日期:2007 卷标:129(29) 页码:9137-9143]
6837-05-4 = 86-34-0 反应条件:1.1 Reagents: Sodium Hydride Catalysts: Acetonitrile,(Oc-6-22)-Dihydrotetrakis(Triphenylphosphine)Ruthenium,1H-Imidazolium,1,3-Bis(1-Methylethyl)-,Bromide (1:1) Solvents: Toluene; 20 Min,Reflux1.2 24 H,Reflux 标题:Synthesis Of Cyclic Imides From Simple Diols 作者:Zhang,Jian; Et Al 参考文献:Angewandte Chemie 日期:2010 卷标:49(36) 页码:6391-6395]
1131-15-3 = 86-34-0 反应条件:1.1 Solvents: 1,2-Dichloroethane,Water; 23 °C; 4 H,80 °C; 80 °C -> 23 °C1.2 Reagents: Acetyl Chloride; Rt; 1 H,80 °C; 80 °C -> 23 °C 标题:Aminoketyl Radicals In Organic Synthesis: Stereoselective Cyclization Of Five- And Six-Membered Cyclic Imides To 2-Azabicycles Using Smi2-H2O 作者:Shi,Shicheng; Et Al 参考文献:Organic Letters 日期:2015 卷标:17(20) 页码:5144-5147]
13706-68-8 = 86-34-0 反应条件:1.1 Catalysts: Sulfuric Acid Solvents: Acetic Acid; 1 H,Reflux; Cooled1.2 Reagents: Sodium Bicarbonate Solvents: Water2.1 Reagents: Potassium Carbonate Solvents: Acetone; Overnight,Reflux 标题:Light-Induced Divergent Cyanation Of Alkynes Enabled By Phosphorus Radicals 作者:Zhang,Yanyan; Et Al 参考文献:Angewandte Chemie 日期:2022 卷标:61(50)]
22903-00-0 = 86-34-0 反应条件:1.1 Reagents: Potassium Carbonate Solvents: Acetone2.1 Reagents: Acetic Acid,Zinc Solvents: Acetic Acid 标题:Synthesis Of Methylthiomaleimides For The Preparation Of Pyridazines And Related Compounds 作者:Tominaga,Yoshinori; Et Al 参考文献:Journal Of Heterocyclic Chemistry 日期:2002 卷标:39(3) 页码:571-591]
49601-28-7 = 86-34-0 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Methanol2.1 Reagents: Potassium Carbonate Solvents: Acetone3.1 Reagents: Acetic Acid,Zinc Solvents: Acetic Acid 标题:Synthesis Of Methylthiomaleimides For The Preparation Of Pyridazines And Related Compounds 作者:Tominaga,Yoshinori; Et Al 参考文献:Journal Of Heterocyclic Chemistry 日期:2002 卷标:39(3) 页码:571-591]
📜1-Methyl-3-Methylsulfanyl-4-Phenylpyrrole-2,5-Dione置于溶剂黄146,锌体系中,化学反应 1.0H,以93%的收率获得产物苯琥胺 参考文献:Synthesis Of 3-Methylthio-4-Aryl-3-Pyrroline-2,5-Diones And 3-Arylpyrrolidine-2,5-Diones By Reaction Of Nitroketene Dithioacetal With Arylacetonitriles 标题:Synthesis Of 3-Methylthio-4-Aryl-3-Pyrroline-2,5-Diones And 3-Arylpyrrolidine-2,5-Diones By Reaction Of Nitroketene Dithioacetal With Arylacetonitriles 摘要:The Reaction Of Nitroketene Dithioacetal (1A),I.E.,2,2-Bis(Methylthio)-1-Nitroethylene,With Arylacetonitriles (2A-I) In The Presence Of The Base Like Sodium Hydroxide Gave 4-Nitrobut-2-Enenitriles (3A-I) Which Were Converted Into 5-Hydroxyimino-4-Methylthio-3-Phenyl-3-Pyrrolin-2-Ones (4A-I) Under Refluxing In Methanol. Title Compounds (5A-I) Were Readily Obtained By The Treatment Of 4A-I With Hydrochloric Acid And Were Finally Led To N-Methylated Products (6A-I) With Methyl Iodide. The Reduction Of Maleimides (4-6) With Zinc Dust In Acetic Acid Afforded The Corresponding 3-Arylpyrrolidine-2,5-Diones (7A-I) That Can Be Converted To Pharmacologycally Active Compounds Like Mesembrines. DOI:10.3987/com-01-9336
专利号:US-2008214827-A1 优先权日:2004-02-03 标 题:Synthesis of Cyanoimino-Benzoimidazoles 发明人:GOEHRING R RICHARD; WHITEHEAD JOHN; SHAO BIN 权利人:EURO CELTIQUE SA 摘要:Disclosed in certain embodiments is a process for synthesizing a compound of formula (V) and salts thereof.
专利号:WO-2012002913-A1 优先权日:2010-07-02 标 题:Process of forming a cyclic imide 发明人:HONG SOON HYEOK; ZHANG JIAN; MUTHAIAH SENTHILKUMAR; GHOSH SUBHASH CHANDRA 权利人:UNIV NANYANG TECH; HONG SOON HYEOK; ZHANG JIAN; MUTHAIAH SENTHILKUMAR; GHOSH SUBHASH CHANDRA 摘要:A process is provided for the synthesis of a cyclic imide. A primary amine and a diol compound are contacted in the presence of a Ruthenium (II) complex. The Ruthenium (II) catalyst includes at least one of an alicyclic ligand, an aromatic ligand, an arylalicyclic ligand, an arylaliphatic ligand and a phosphine ligand.
专利号:CA-2555219-A1 优先权日:2004-02-03 标 题 :Synthesis of cyanoimino-benzoimidazoles
专利号:US-8945508-B2 优先权日:2009-10-13 标 题 :Dendrimer compositions and methods of synthesis 发明人:BAKER JR JAMES R; HUANG BAOHUA 权利人:BAKER JR JAMES R; HUANG BAOHUA; UNIV MICHIGAN 摘要:The present invention relates to novel dendrimer compounds and methods of synthesizing the same. In particular, the present invention is directed to novel polyamidoamine (PAMAM) dendrimers, novel dendrimer branching units, methods for synthesizing such novel PAMAM dendrimers and functionalized dendrimers, as well as systems and methods utilizing the dendrimers (e.g., in diagnostic and/or therapeutic settings (e.g., for the delivery of therapeutics, imaging, and/or targeting agents (e.g., in disease diagnosis and/or therapy, etc.))).
专利号:WO-2005075459-A1 优先权日:2004-02-03 标题:Synthesis of cyanoimino-benzoimidazoles
专利号:US-2013030282-A1 优先权日:2011-07-18 标题:Synthesis and characterization of near ir fluorescent magnetic and non-magnetic albumin nanoparticles for biomedical applications 发明人:MARGEL SHLOMO; COHEN SARIT; SALKMON ENAV COREM; PELLACH MICHAL 权利人:UNIV BAR ILAN; MARGEL SHLOMO; COHEN SARIT; SALKMON ENAV COREM; PELLACH MICHAL 摘要:The present invention discloses Near Infrared (NIR) fluorescent albumin nanoparticles having a structure selected from a core structure or a core-shell structure. Also disclosed are a process of preparing these NIR fluorescent albumin nanoparticles, and a method of in vivo detection of pathologies, in particular cancer pathology, by using administering these NIR fluorescent albumin nanoparticles to a patient.
1: Ma C, Xiong J, Su H, Li H. The underlying molecular mechanism and drugs for treatment in adrenal cortical carcinoma. Int J Med Sci. 2021 Jun 16;18(13):3026-3038. doi: 10.7150/ijms.60261. 2: Wang S, Meng X, Wang Y, Liu Y, Xia J. HPO-Shuffle: an associated gene prioritization strategy and its application in drug repurposing for the treatment of canine epilepsy. Biosci Rep. 2019 Sep 6;39(9):BSR20191247. doi: 10.1042/BSR20191247. 3: Ali MA, Siddiki SM, Kon K, Hasegawa J, Shimizu K. Versatile and sustainable synthesis of cyclic imides from dicarboxylic acids and amines by Nb2O5 as a base-tolerant heterogeneous Lewis acid catalyst. Chemistry. 2014 Oct 27;20(44):14256-60. doi: 10.1002/chem.201404538. Epub 2014 Sep 15. 18(2):183-6. Chinese. 74(1):77-88. doi: 10.1016/0300-483x(92)90045-g. 10(3):203-9. doi: 10.1002/jat.2550100311. 10(2):143-52. doi: 10.1002/jat.2550100214. 11(3):337-42. doi: 10.1097/00007691-198905000-00018. 240(1):216-22. 6(5):349-56. doi: 10.1002/jat.2550060509. 4(3):601-16. 8(3):125-43. doi: 10.3109/01480548508999165.
合成参考文献
摘要:Arzneimittel-Forschung. Drug Research., 23(377), 1973 [] 参考文献:10.1212/wnl.4.2.137 摘要:SMITH B, FORSTER FM. Mysoline and milontin, two new medicines for epilepsy. Neurology. 1954 Feb;4(2):137–42. doi: 10.1212/wnl.4.2.137. 摘要:LEMERE F. Milontin in treatment of petit mal epilepsy. Northwest Med. 1954 May;53(5):482. 参考文献:10.1016/s0022-3565(25)11274-3 摘要:Glazko AJ, Dill WA, Wolf LM, Miller CA. THE DETERMINATION AND PHYSIOLOGICAL DISPOSITION OF MILONTIN (N-METHYL-α-PHENYLSUCCINIMIDE). The Journal of Pharmacology and Experimental Therapeutics. 1954 Aug;111(4):413–24. doi: 10.1016/s0022-3565(25)11274-3. 参考文献:10.2165/00003088-199223020-00005 摘要:Murray M. P450 enzymes. Inhibition mechanisms, genetic regulation and effects of liver disease. Clin Pharmacokinet. 1992 Aug;23(2):132–46. doi: 10.2165/00003088-199223020-00005.