合成目标产物 2,4-Dimethylimidazole 主要起始原料 D(+)-Glucose And Acetaldehyde
2450-71-7 + 1000-84-6 = 930-62-1 [标题:Reaction Conditions 标题:New Process For Synthesis Of Imidazole Derivatives 作者:Eloy,F.; Deryckere,A.; Maffrand,J. P. 参考文献:European Journal Of Medicinal Chemistry 日期:1974 卷标:9(6) 页码:602-6]
83576-22-1 = 930-62-1 反应条件:1.1 Reagents: Water Solvents: Water 标题:A New Synthesis Of Imidazoles 作者:Casey,Michael; Moody,Christopher J.; Rees,Charles W. 参考文献:Journal Of The Chemical Society 日期:1982 卷标:(13) 页码:714-15]
78-90-0 = 930-62-1 反应条件:1.1 Catalysts: Ap 64K 标题:Catalytic Synthesis Of C-Alkylimidazoles In The Presence Of Platinum/alumina Catalysts 作者:Gitis,K. M.; Neumoeva,G. E.; Raevskaya,N. I.; Arutyunyants,G. A.; Isagulyants,G. V. 参考文献:Izvestiya Akademi Nauk 日期:1992 卷标:(4) 页码:932-40]
52726-31-5 = 930-62-1 反应条件:1.1 Reagents: Triethylsilane Catalysts: Palladium Solvents: Tetrahydrofuran; 24 H,Rt 标题:Deprotection Of N-Benzylbenzimidazoles And N-Benzylimidazoles With Triethylsilane And Pd/c 作者:Graham,Thomas H. 参考文献:Tetrahedron Letters 日期:2015 卷标:56(21) 页码:2688-2690]
930-61-0 = 930-62-1 反应条件:1.1 Catalysts: Chloroform 标题:Reactions Of Halomethanes In The Vapor Phase. Part 5. The Reactions Of Imidazolines,Anils,And 1-Methylimidazole With Chloroform At 550°C,And A Comparison With Their Liquid-Phase Reactions With Trichloroacetate Ion Or Hexachloroacetone And Base 作者:Busby,Reginald E.; Khan,Mohammad A.; Khan,Mohammad R.; Parrick,John; Shaw,C. J. Granville 参考文献:Journal Of The Chemical Society 日期:1980 卷标:(7) 页码:1431-5]
= 930-62-1 [标题:Reaction Conditions 标题:An Approach To The Cyclopeptide Alkaloids (Phencyclopeptines) Via Heterocyclic Diamide/dipeptide Equivalents. Preparation And N-Alkylation Studies Of 2,4(5)-Disubstituted Imidazoles 作者:Lipshutz,Bruce H.; Morey,Matthew C. 参考文献:Journal Of Organic Chemistry 日期:1983 卷标:48(21) 页码:3745-50]
= 930-62-1 [标题:Reaction Conditions 标题:Imidazoles By Reaction Of Acetalated α-Dicarbonyl Compounds With Ammonia And/or Ammonium Salts And Aldehydes 参考文献:Federal Republic Of Germany]
= 930-62-1 反应条件:1.1 Reagents: Nitrosonium Tetrafluoroborate,Vitride 标题:Reductions By Metal Alkoxyaluminum Hydrides. Part Ii. Carboxylic Acids And Derivatives,Nitrogen Compounds,And Sulfur Compounds 作者:Malek,Jaroslav 参考文献:Organic Reactions (Hoboken 日期:1988 卷标:36]
= 930-62-1 [标题:Reaction Conditions 标题:Reaction Of Nitrosonium Fluoborate With Olefins In Nitrile Media. Two-Step Synthesis Of Imidazoles From Olefins 作者:Scheinbaum,Monte L.; Dines,Martin B. 参考文献:Tetrahedron Letters 日期:1971 卷标:(24) 页码:2205-8]
83576-22-1 = 930-62-1 [标题:Reaction Conditions 标题:Synthesis Of Imidazoles From Alkenes 作者:Casey,Michael; Moody,Christopher J.; Rees,Charles W. 参考文献:Journal Of The Chemical Society 日期:1984 卷标:(8) 页码:1933-41]
592-20-1 = 930-62-1 [标题:Reaction Conditions 标题:Product Class 3: Imidazoles 作者:Grimmett,M. R. 参考文献:Science Of Synthesis 日期:2002 卷标:12 页码:325-528]
= 930-62-1 反应条件:1.1 Reagents: Lithium Sulfide Solvents: Benzene,Acetonitrile,2-Amino-1-Butanol; 3 D,85 °C 标题:Preparation Method Of Neutron Shielding Material Based On Metal Boron-Imidazole Framework 参考文献:China]
78-98-8 = 930-62-1 反应条件:1.1 Reagents: Sodium Bicarbonate 标题:Chemoselective And Living/controlled Polymerization Of Polar Divinyl Monomers By N-Heterocyclic Olefin Based Classical And Frustrated Lewis Pairs 作者:Zhao,Wuchao; Wang,Qianyi; He,Jianghua; Zhang,Yuetao 参考文献:Polymer Chemistry 日期:2019 卷标:10(31) 页码:4328-4335]
78-98-8 = 930-62-1 反应条件:1.1 Reagents: Ammonium Oxalate,Ammonia Solvents: Water; 3 H,45 °C; 2 H,45 °C 标题:Process For Preparation Of Dialkyl Imidazole 参考文献:China]
83505-98-0 = 930-62-1 反应条件:1.1 Solvents: Ethanol 标题:Synthesis Of Some Alkyl- And Arylimidazoles 作者:Watanabe,T.; Nishiyama,J.; Hirate,R.; Uehara,K.; Inoue,M.; Et Al 参考文献:Journal Of Heterocyclic Chemistry 日期:1983 卷标:20(5) 页码:1277-81]
= 930-62-1 [标题:Reaction Conditions 标题:Manufacture Of Stable 2-Ethyl-4-Methylimidazole Compositions 参考文献:Japan]
= 930-62-1 [标题:Reaction Conditions 标题:Method For The Preparation Of Imidazoles By Dehydrogenation Of Imidazolines 参考文献:United States]
= 930-62-1 [标题:Reaction Conditions 标题:Preparation Of 4-Methylimidazoles From Methylglyoxal,Aldehydes,And Ammonia 参考文献:Japan
专利号:US-2023312617-A1 优先权日:2020-07-25 标题 :Process for synthesis of organosilicon compounds from halosilanes 发明人:DOLAI SUKANTA; BHAT SHREEDHAR; TARAFDAR GOURAV 权利人:MOMENTIVE PERFORMANCE MAT INC 摘要:A process for synthesis of an organosilicon compound is provided herein. Also, novel organosilicon compounds prepared by the present process is provided herein. The process comprises the reaction of a halosilane with an organofunctional alkyl halide in the presence of a metal catalyst, a promoter, and an optional co-catalyst. The process provides an efficient synthetic route to produce organosilicon compounds. The process also allows synthesis of organosilicon compounds with a plurality of different functional groups.
专利号:US-2023286918-A1 优先权日:2020-07-02 标 题:Manufacturing process for 3,5-dichloropicolinonitrile for synthesis of vadadustat 发明人:JURKAUSKAS VALDAS; JUNG YOUNG CHUN; KWON TAESOO; KANNAN ARUNACHALAM; GONDI VIJAYA BHASKER 权利人:AKEBIA THERAPEUTICS INC 摘要:Disclosed herein are methods and processes of preparing vadadustat or a pharmaceutically acceptable salts thereof, and intermediates (e.g., a compound of Formula (I), (I-F), (II), or (IV), or a pharmaceutically acceptable salts thereof) useful for the synthesis of vadadustat.
专利号:US-8637695-B2 优先权日:2011-12-30 标 题:Synthesis of organohalosilane monomers from conventionally uncleavable Direct Process Residue 发明人:LEWIS KENRICK MARTIN; NEELY JOHN DAVID 权利人:LEWIS KENRICK MARTIN; NEELY JOHN DAVID; MOMENTIVE PERFORMANCE MAT INC 摘要:Disclosed herein is a catalytic process for the synthesis of organohalosilane monomers from tetraorganodihalodisilanes and other compounds that are not cleaved during the conventional hydrochlorination of Direct Process Residue. The process is characterized by the use of a catalyst containing (1) one or more heterocyclic amines and/or one or more heterocyclic ammonium halides, and (2) one or more quaternary Group 15 onium compounds.
专利号:US-12157751-B2 优先权日:2021-05-12 标题 :Process for the synthesis of oligomeric siloxane having sulfone moiety, and silicon-containing compounds having sulfone moiety 发明人:SINGHAL PRAVEEN KUMAR; TARAFDAR GOURAV; RAMESH APEKSHA 权利人:MOMENTIVE PERFORMANCE MAT INC 摘要:There is provided herein a process for the synthesis of sulfonyl silanes. There is also provided herein various sulfenylated and sulfonylated silicon-containing compounds made by the process.
专利号:EP-0310950-B1 优先权日:1983-11-18 标题 :Quinoline intermediates for the synthesis of 1H-imidazo[4,5-c]quinolines and 1H-imidazo[4,5-c]quinolin-4-amimes 摘要:Compounds of the types (I) and (II) are disclosed, wherein each R5 is independently selected from the group consisting of alkyl of one to about four carbon atoms, alkoxy of one to about four carbon atoms and halogen, and n is an integer from 0 to 2, with the proviso that if n is 2, then said R5 substituents together contain no more than 6 carbon atoms; R6 is selected from the group consisting of hydroxyalkyl of one to about six carbon atoms and cyclohexylmethyl; and R7 is selected from the group consisting of alkyl of one to about four carbon atoms and hydrogen. These compounds may be used as intermediates for the synthesis of 1H-imidazo[4,5-c]quinoline derivatives.
专利号:US-2002161219-A1 优先权日:2001-02-21 标 题:Non-enzymatic large scale synthesis of RNA 发明人:KANAVARIOTI ANASTASSIA; DEAMER DAVID W; MONNARD PIERRE-ALAIN M; BERNASCONI CLAUDE F 摘要:This invention pertains to the development of methods that accomplish efficient, non-enzymatic, nucleic acid-directed (e.g. RNA-directed) nucleic acid (e.g. RNA) synthesis. In certain embodiments the methods provide conditions that favor oligouridylate synthesis with excellent yield and, at least, up to 30% regioselectivity favoring the RNA linkage. The methods preferably involve contacting, in the presence of lead ions (Pb 2+ ) and/or tin ions (Sn 2+ ) and, optionally, magnesium ions (Mg 2+ ), a template nucleic acid with a nucleotide derivatized with an imidazolide.