合成目标产物 Enrofloxacin 主要起始原料 1-Ethylpiperazine And 7-Chloro-1-Cyclopropyl-6-Fluoro-1,4-Dihydro-4-Oxoquinoline-3-Carboxylic Acid
5308-25-8 + 86393-33-1 = 93106-60-6 反应条件:1.1 Catalysts: Molybdate(42-),Triacontakis[μ-(Acetato-Ko:Ko′)]Doheptacontaaquaoctacontahecta-μ... Solvents: Water; 30 Min,Reflux 标题:Fast And Green Method To Synthesis Of Quinolone Carboxylic Acid Derivatives Using Giant-Ball Nanoporous Isopolyoxomolybdate As Highly Efficient Recyclable Catalyst In Refluxing Water 作者:Mirzaie,Yahya; Lari,Jalil; Vahedi,Hooshang; Hakimi,Mohammad; Nakhaei,Ahmad; Et Al 参考文献:Journal Of The Mexican Chemical Society 日期:2017 卷标:61(1) 页码:35-40]
5308-25-8 + 86393-33-1 = 93106-60-6 反应条件:1.1 25 Min,150 °C 标题:Conventional And Microwave-Assisted Synthesis Of Quinolone Carboxylic Acid Derivatives 作者:Mirzaie,Y.; Lari,J.; Vahedi,H.; Hakimi,M. 参考文献:Russian Journal Of General Chemistry 日期:2016 卷标:86(12) 页码:2865-2869]
105392-26-5 + 5308-25-8 = 93106-60-6 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Toluene; 4 H,Reflux1.2 Reagents: Hydrochloric Acid Solvents: Water1.3 Solvents: Water; 1 H,Reflux; 14 H,115 °C 标题:Convenient One Pot Synthesis Of Some Fluoroquinolones In Aqueous Media 作者:Abaee,M. Saeed; Sharifi,Ruhollah; Borhani,Shahin; Heravi,Majid M.; Motahari,Hossein 参考文献:Heterocyclic Communications 日期:2005 卷标:11(5) 页码:415-418]
93107-08-5 = 93106-60-6 反应条件:1.1 Reagents: Diisopropylethylamine Catalysts: Potassium Iodide Solvents: Acetonitrile,Water; 0 °C; 16 H,Rt 标题:Pharmacological Characterization Of 7-(4-(Piperazin-1-Yl)) Ciprofloxacin Derivatives: Antibacterial Activity,Cellular Accumulation,Susceptibility To Efflux Transporters,And Intracellular Activity 作者:Marquez,Beatrice; Pourcelle,Vincent; Vallet,Coralie M.; Mingeot-Leclercq,Marie-Paule; Tulkens,Paul M.; Et Al 参考文献:Pharmaceutical Research 日期:2014 卷标:31(5) 页码:1290-1301]
107884-20-8 = 93106-60-6 反应条件:1.1 Reagents: Sodium Hydroxide Solvents: Water1.2 Reagents: Acetic Acid 标题:An Improved Process For The Preparation Of Quinolone Derivatives,E.G. Ciprofloxacin 参考文献:World Intellectual Property Organization]
= 93106-60-6 [标题:Reaction Conditions 标题:Preparation Of Specific Conjugation Bridge Linkers And Immunoconjugates And Methods Of Using Them 参考文献:World Intellectual Property Organization]
= 93106-60-6 [标题:Reaction Conditions 标题:Preparation Of Bridge Linkers Used For Specific Conjugation Of A Cytotoxic Agent To A Cell-Binding Molecule 参考文献:World Intellectual Property Organization]
5308-25-8 + 86393-33-1 = 93106-60-6 反应条件:1.1 Catalysts: Zirconium Dioxide (Sulfonic Acid Derivative Absorbed On Ferrite) Solvents: Water; 19 Min,Reflux 标题:Nano-Fe3O4@zro2-So3H As Highly Efficient Recyclable Catalyst For The Green Synthesis Of Fluoroquinolones 作者:Nakhaei,Ahmad; Ramezani,Shirin; Shams-Najafi,Sayyed Jalal; Farsinejad,Sadaf 参考文献:Letters In Organic Chemistry 日期:2018 卷标:15(9) 页码:739-746]
5308-25-8 + 86393-33-1 = 93106-60-6 [标题:Reaction Conditions 标题:New Process For The Preparation Of 1-Cyclopropyl-3-Quinolinecarboxylic Acid Derivatives 参考文献:Spain]
5308-25-8 + 86393-33-1 = 93106-60-6 反应条件:1.1 Solvents: Dimethyl Sulfoxide 标题:Cycloaracylation Of Enamines. I. Synthesis Of 4-Quinolone-3-Carboxylic Acids 作者:Grohe,Klaus; Heitzer,Helmut 参考文献:Liebigs Annalen Der Chemie 日期:1987 卷标:(1) 页码:29-37]
= 93106-60-6 [标题:Reaction Conditions 标题:Preparation Of Bridge Linkers Used For Specific Conjugation Of Two Or More Cytotoxic Agents To A Cell-Binding Molecule 参考文献:World Intellectual Property Organization]
= 93106-60-6 [标题:Reaction Conditions 标题:Preparation Of Novel Bridge Linkers Containing An Acetylenedicarbonyl Group For Specific Conjugation Of A Cytotoxic Agent To A Cell-Binding Molecule 参考文献:World Intellectual Property Organization]
= 93106-60-6 [标题:Reaction Conditions 标题:Preparation Of Hydrophilic Linkers For The Conjugation Of A Cytotoxic Agent Or A Chromophore To A Cell-Binding Molecule 参考文献:World Intellectual Property Organization
专利号:US-11274081-B2 优先权日:2016-05-30 标 题:Process for the synthesis of ivacaftor 发明人:REDDY DUMBALA SRINIVASA; KULKARNI AMOL ARVIND; NATARAJAN VASUDEVAN; SHARMA MRITYUNJAY KESHAVPRASAD 权利人:COUNCIL SCIENT IND RES 摘要:The present disclosed an improved process for the synthesis of ivacaftor starting from indole acetic acid ester which can be performed in batch as well as continuous flow synthesis. The present invention further disclosed to a continuous process for the synthesis of compound of formula (II) or formula (III) from compound of formula (I) in continuous flow reactor.
专利号:US-10768157-B2 优先权日:2015-10-20 标 题:Materials and methods for the detection of trace amounts of substances in biological and environmental samples 发明人:KABIR ABUZAR; FURTON KENNETH G 权利人:KABIR ABUZAR; FURTON KENNETH G; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES 摘要:The subject invention provides chemical compositions and synthesis strategies to create molecularly imprinted polymers (MIPs) via sol-gel processes. In a specific embodiment, the subject invention utilizes a(n) organic, inorganic, or metallic template analyte to create a hybrid organic-inorganic or inorganic three-dimensional network possessing cavities complementary to the shape, size, and functional orientation of the template molecule or ions. The subject invention further pertains to the use of the novel MIPs as selective solid phase extraction (SPE) sorbents for pre-concentration and clean-up of trace substances in biological and environmental samples. Synthesis of other molecularly imprinted polymers with environmental, pharmaceutical, chemical, clinical, toxicological, and national security implications can be conducted in accordance with the teachings of the subject invention.
专利号:US-9772338-B2 优先权日:2015-10-20 标题 :Materials and methods for the detection of trace amounts of substances in biological and environmental samples 发明人:KABIR ABUZAR; FURTON KENNETH G 权利人:KABIR ABUZAR; FURTON KENNETH G; UNIV FLORIDA INT 摘要:The subject invention provides chemical compositions and synthesis strategies to create molecularly imprinted polymers (MIPs) via sol-gel processes. In a specific embodiment, the subject invention utilizes a(n) organic, inorganic, or metallic template analyte to create a hybrid organic-inorganic or inorganic three-dimensional network possessing cavities complementary to the shape, size, and functional orientation of the template molecule or ions. The subject invention further pertains to the use of the novel MIPs as selective solid phase extraction (SPE) sorbents for pre-concentration and clean-up of trace substances in biological and environmental samples. Synthesis of other molecularly imprinted polymers with environmental, pharmaceutical, chemical, clinical, toxicological, and national security implications can be conducted in accordance with the teachings of the subject invention.
专利号:US-11332444-B2 优先权日:2018-04-25 标题:Method for the hydrolysis of quinolonecarboxylic esters 发明人:FEY PETER; BERWE MATHIAS; WIRTHS Joerg; WISCHNAT RALF; LONGERICH MARKUS; DIETZEL ANTJE 权利人:BAYER ANIMAL HEALTH GMBH 摘要:Quinolonecarboxylic esters of the general formula (II) are hydrolyzed to quinolonecarboxylic acids of the general formula (I):The method comprises the step A):A) reacting compounds of the formula (II) with a mixture comprising acetic acid, sulfuric acid and waterIn step A), ≥30 to ≤40 mol of acetic acid, ≥0.3 to ≤1 mol of sulfuric acid and ≥0.9 to ≤2.5 mol of water are used per mole of compounds of the formula (II). The method is particularly suitable for the synthesis of the intermediate (I) in the synthesis of pradofloxacin.
专利号:WO-2025056767-A1 优先权日:2023-09-15 标题 :Process for the preparation of enantiomerically enriched aliphatic amines 发明人:BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS 权利人:SYNGENTA CROP PROTECTION AG 摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.
专利号:US-8093381-B2 优先权日:2007-05-24 标题:Method of synthesis of fluoroquinolones 发明人:BERTHON-CEDILLE LAURENCE; LEGUERN MARIE-EMMANUELLE; RENAUD GILLES; TOMBRET FRANCIS 权利人:BERTHON-CEDILLE LAURENCE; LEGUERN MARIE-EMMANUELLE; RENAUD GILLES; TOMBRET FRANCIS; BIOCODEX 摘要:The invention relates to a method of preparation of fluoroquinolones of formula (I) from compounds of formula (II): n nin which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and X are as defined in Claim 1.
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合成参考文献
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