1211519-08-2 = 943541-20-6 反应条件:1.1 Reagents: Potassium Tert-Butoxide Catalysts: 18-Crown-6 Solvents: Diethyl Ether; 20 Min,Rt; Rt -> 0 °C1.2 0 °C; Overnight,0 °C -> Rt 标题:1,2,4-Triazolo[4,3-B]Pyridazine Derivatives As Highly Selective C-Met Kinase Inhibitors And Their Preparation,Pharmaceutical Compositions And Use In The Treatment Of Cancer 参考文献:World Intellectual Property Organization]
141-30-0 + 269410-08-4 = 943541-20-6 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: [1,1′-Bis(Diphenylphosphino)Ferrocene]Dichloropalladium Solvents: 1,4-Dioxane,Water; 5 H,90 °C 标题:Discovery Of Substituted Pyrazol-4-Yl Pyridazinone Derivatives As Novel C-Met Kinase Inhibitors 作者:Kim,Eun-Young; Kang,Seung-Tae; Jung,Heejung; Park,Chi Hoon; Yun,Chang-Soo; Et Al 参考文献:Archives Of Pharmacal Research 日期:2016 卷标:39(4) 页码:453-464]
135034-10-5 + 761446-44-0 = 943541-20-6 反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Dichlorobis(Triphenylphosphine)Palladium Solvents: 1,2-Dimethoxyethane; Rt -> 80 °C; 3 H,80 °C 标题:Preparation Of Pyridazinones As Antitumor Agents 参考文献:World Intellectual Property Organization]
= 943541-20-6 [标题:Reaction Conditions 标题:Preparation Of Polymorphic And Hydrate Forms,Salts Of 6-[difluoro[6-(1-Methyl-1H-Pyrazol-4-Yl)[1,2,4]Triazolo[4,3-B]Pyridazin-3-Yl]Methyl]Quinoline For Treatment Of Cell Proliferative Disorder 参考文献:United States]
= 943541-20-6 [标题:Reaction Conditions 标题:Preparation Of Pyridazinones As Antitumor Agents 参考文献:Germany]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: [1,1′-Bis(Diphenylphosphino)Ferrocene]Dichloropalladium Solvents: 1,4-Dioxane,Water; 10 H,90 °C 标题:Preparation Of Quinoline Derivatives As Parp-1 And C-Met Dual-Target Inhibitors For Treating Cancer 参考文献:China]
135034-10-5 + 761446-44-0 = 943541-20-6 反应条件:1.1 Reagents: Benzyltriethylammonium Chloride,Triphenylphosphine,Tripotassium Phosphate Catalysts: Palladium Diacetate Solvents: Tetrahydrofuran,Water; 16 H,65 °C; 65 °C -> 60 °C1.2 Reagents: Sodium Chloride Solvents: Water; 15 Min,60 °C; 60 °C -> 45 °C 标题:Preparation Of Polymorphic And Hydrate Forms,Salts Of 6-[difluoro[6-(1-Methyl-1H-Pyrazol-4-Yl)[1,2,4]Triazolo[4,3-B]Pyridazin-3-Yl]Methyl]Quinoline For Treatment Of Cell Proliferative Disorder 参考文献:World Intellectual Property Organization]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Dichloro[1,1′-Bis(Diphenylphosphino)Ferrocene]Palladium(Ii) Dichloromethane Addu... Solvents: 1,4-Dioxane,Water; 4 H,80 °C 标题:Preparation Of Bicyclic Triazoles As Protein Kinase Modulators 参考文献:World Intellectual Property Organization]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: [1,1′-Bis(Diphenylphosphino)Ferrocene]Dichloropalladium Solvents: 1,4-Dioxane,Water; Rt -> 80 °C; 10 H,80 °C 标题:Preparation Of Quinoline Derivatives As C-Met Inhibitors For Treatment Of Cancer 参考文献:China]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Sodium Carbonate Catalysts: Tetrakis(Triphenylphosphine)Palladium Solvents: 1,4-Dioxane,Water; Overnight,Rt -> 80 °C 标题:Preparation Of Triazolopyridazines As Tyrosine Kinase Modulators 参考文献:World Intellectual Property Organization]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: [1,1′-Bis(Diphenylphosphino)Ferrocene]Dichloropalladium Solvents: 1,4-Dioxane,Water; 16 H,80 °C 标题:Preparation Of 6-(1-Methyl-1H-Pyrazol-4-Yl)-3-(2-Methyl-2H-Indazol-5-Ylthio)-[1,2,4]Triazolo[4,3-B]Pyridazine As Antitumor Agent 参考文献:World Intellectual Property Organization]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Sodium Carbonate Solvents: 1,4-Dioxane; 1 Min,Rt1.2 Catalysts: Dichlorobis(Triphenylphosphine)Palladium; 15 H,80 °C 标题:Preparation Of A Novel Deuterated Triazolopyridazine As C-Met Kinase Inhibitor For Treating Cancer 参考文献:World Intellectual Property Organization]
761446-44-0 + 141-30-0 = 943541-20-6 反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Tetrakis(Triphenylphosphine)Palladium Solvents: 1,4-Dioxane,Water; 5 H,100 °C 标题:Preparation Of Substituted Piperidinyl-Pyridazinyl Derivatives As Scd1 Inhibitors 参考文献:World Intellectual Property Organization]
135034-10-5 + 761446-44-0 = 943541-20-6 反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Dichlorobis(Triphenylphosphine)Palladium Solvents: 1,2-Dimethoxyethane; Rt -> 80 °C; 3 H,80 °C 标题:Preparation Of Triazolo[4,3-B]Pyridazines As Met Kinase Inhibitors 参考文献:World Intellectual Property Organization]
135034-10-5 + 761446-44-0 = 943541-20-6 反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Dichlorobis(Triphenylphosphine)Palladium Solvents: 1,2-Dimethoxyethane; Rt -> 80 °C; 3 H,80 °C; 80 °C -> Rt 标题:Pyridazinone Derivatives As Met Kinase Inhibitors And Their Preparation And Use In The Treatment Of Cancer 参考文献:World Intellectual Property Organization]
= 943541-20-6 [标题:Reaction Conditions 标题:Preparation Of Triazolo[4,3-B]Pyridazines As Met Kinase Inhibitors 参考文献:Germany
参考文献:10.1007/s12272-015-0703-7 摘要:Kim E, Kang S, Jung H, Park CH, Yun C, Hwang JY, Byun BJ, Lee CO, Kim HR, Ha JD, Ryu DH, Cho SY. Discovery of substituted pyrazol-4-yl pyridazinone derivatives as novel c-Met kinase inhibitors. Archives of Pharmacal Research. 2016 Jan 11;39(4):453–64. doi: 10.1007/s12272-015-0703-7.