78415-72-2 = 80047-24-1 反应条件:1.1 Reagents: Sulfuric Acid; 15 Min,Rt -> 120 °C1.2 Reagents: Ammonium Hydroxide Solvents: Water; Ph 10 标题:Synthesis And Profiling Of A 3-Aminopyridin-2-One-Based Kinase Targeted Fragment Library: Identification Of 3-Amino-5-(Pyridin-4-Yl)Pyridin-2(1H)-One Scaffold For Monopolar Spindle 1 (Mps1) And Aurora Kinases Inhibition 作者:Fearon,Daren; Westwood,Isaac M.; Van Montfort,Rob L. M.; Bayliss,Richard; Jones,Keith; Et Al 参考文献:Bioorganic & Medicinal Chemistry 日期:2018 卷标:26(11) 页码:3021-3029]
129090-34-2 = 80047-24-1 反应条件:1.1 Reagents: Sodium Nitrite,Hydrochloric Acid,Ammonia 标题:Preparation Of 5-Aryl-1,2-Dihydropyrid-2-Ones As Cardiotonics 参考文献:German Democratic Republic]
78415-72-2 = 80047-24-1 反应条件:1.1 Reagents: Sulfuric Acid Solvents: Water; 30 Min,100 °C; 100 °C -> 0 °C1.2 Reagents: Water1.3 Reagents: Ammonium Hydroxide Solvents: Water; Ph 10 标题:Purification Of 1,6-Dihydro-2-Methyl-6-Oxo[3,4'-Bipyridine]-5-Carbonitrile (Milrinone) And Synthesis Of Its Usp Impurity A [i.E.,1,6-Dihydro-2-Methyl-6-Oxo-[3,4'-Bipyridine]-5-Carboxamide] 作者:Dai,Xuyong; Guo,Peng; Li,Liwei 参考文献:Zhongguo Yaoxue Zazhi (Beijing 日期:2007 卷标:42(18) 页码:1436-1437]
78415-72-2 = 80047-24-1 反应条件:1.1 Reagents: Sulfuric Acid 标题:Bipyridine Cardiotonics: The Three-Dimensional Structures Of Amrinone And Milrinone 作者:Robertson,David W.; Beedle,E. E.; Swartzendruber,John K.; Jones,Noel D.; Elzey,T. K.; Et Al 参考文献:Journal Of Medicinal Chemistry 日期:1986 卷标:29(5) 页码:635-40
📜米力农置于硫酸体系中,化学反应 0.25H,以72%的收率获得产物米力农杂质a 参考文献:Synthesis And Profiling Of A 3-Aminopyridin-2-One-Based Kinase Targeted Fragment Library: Identification Of 3-Amino-5-(Pyridin-4-yl)Pyridin-2(1H)-One Scaffold For Monopolar Spindle 1 (Mps1) And Aurora Kinases Inhibition 标题:Synthesis And Profiling Of A 3-Aminopyridin-2-One-Based Kinase Targeted Fragment Library: Identification Of 3-Amino-5-(Pyridin-4-yl)Pyridin-2(1H)-One Scaffold For Monopolar Spindle 1 (Mps1) And Aurora Kinases Inhibition 摘要:Screening A 3-Aminopyridin-2-One Based Fragment Library Against A 26-Kinase Panel Representative Of The Human Kinome Identified 3-Amino 5 (1-Methyl-1H-Pyrazol-4-yl)Pyridin-2(1H)-One (2) And 3-Amino-5(Pyridin-4-yl)Pyridin-2(1H)-One (3) As Ligand Efficient Inhibitors Of The Mitotic Kinase Monopolar Spindle 1 (Mps1) And The Aurora Kinase Family. These Kinases Are Well Recognised As Attractive Targets For Therapeutic Intervention For Treating Cancer. Elucidation Of The Binding Mode Of These Fragments And Their Analogues Has Been Carried Out By X-Ray Crystallography. Structural Studies Have Identified Key Interactions With A Conserved Lysine Residue And Have Highlighted Potential Regions Of Mps1 Which Could Be Targeted To Improve Activity And Selectivity. (C) 2018 The Authors. Published By Elsevier Ltd. DOI:10.1016/j.Bmc.2018.04.033
专利号:US-3683014-A 优先权日:1970-10-14 标题:Derivatives of 2-amino-3-sulfopropionic acid 发明人:YANG MEILING T 权利人:ETHYL CORP 摘要:To obviate eutrophication of water, non-phosphorus detergent builders are provided. These are the water-soluble salts of 2-(N, N-di-(carboxymethyl))amino-3-sulfopropionic acid (e.g., the tetrasodium salt thereof). Conventional detergent actives may be used with these builders. Synthesis of the builders is described.
专利号:US-3637511-A 优先权日:1969-05-19 标题:Detergent formulations 发明人:YANG MEILING T 权利人:ETHYL CORP 摘要:To obviate eutrophication of water, nonphosphorus detergent builders are provided. These are the water-soluble salts of N,N,di(carboxymethyl)-aspartic acid (e.g., the tetrasodium salt thereof). Conventional detergent actives may be used with these builders. Synthesis of the builders is described.
专利号:CN-108329445-A 优先权日:2017-01-20 标题:A kind of phenolic resin esterified benzene sulfonate and its synthesis method, hydrophilic plate for printing and its application, and printing plate
参考文献:10.1016/j.bmc.2018.04.033 摘要:Fearon D, Westwood IM, van Montfort RLM, Bayliss R, Jones K, Bavetsias V. Synthesis and profiling of a 3-aminopyridin-2-one-based kinase targeted fragment library: Identification of 3-amino-5-(pyridin-4-yl)pyridin-2(1H)-one scaffold for monopolar spindle 1 (MPS1) and Aurora kinases inhibition. Bioorganic & Medicinal Chemistry. 2018 Jul;26(11):3021–9. doi: 10.1016/j.bmc.2018.04.033.