CAS: 80370-57-6; Ceftiofur

该化合物是一种主要用于牲畜特别是牛和猪牲畜细菌感染治疗的兽医药物中广泛谱谱状的甲状腺素抗生素,对各种抗菌剂和克型阴性细菌有效,对管理呼吸系统和其他感染很有价值;Ceftiofur通过抑制细菌细胞壁合成,导致细胞分解和死亡;该化合物一般通过注射施用,已知动物体内的毒性相对较低;其药理学允许有效的组织分布,并经常用于提供延长释放特性的配方;Ceftiofur还因其对某些病原体采取特定行动而减少抗生素抗药性风险的能力而引人注目;然而,在生产食物的动物中管制其使用,以尽量减少肉类和牛奶中的抗生素残留,在动物加工用于食品之前必须坚持停用时间.

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CAS号63527-52-6 头孢噻肟 | CAS号4741-45-1 2-呋喃硫代羧酸 | CAS号64485-93-4 头孢噻肟钠 | CAS号111230-59-2 (Z)-4-氯-2-甲氧基亚氨...

合成工艺路线路线简述

  • 80756-85-0 + 80370-59-8 = 80370-57-6
    反应条件:1.1 Solvents: Dichloromethane; 3 H,40 °C1.2 Reagents: Hydrochloric Acid Solvents: Water
    标题:Preparation Of Ceftiofur Sodium Salt
    作者:Cao,Yujian; Et Al
    参考文献:Zhongguo Kangshengsu Zazhi 日期:2003 卷标:28(11) 页码:645-646
7-[2-(2-Aminothiazol-4-yl)-2-Methoxyiminoacetamido]-3-[(Fur-2-Ylcarbonyl)Thiomethyl]-3-Cephem-4-Carboxylic Acid P-Methoxybenzyl Ester置于三氟乙酸,苯甲醚体系中,用 二氯甲烷 作为反应溶剂,化学反应 1.67H,反应生成 头孢噻呋
参考文献:New Method For The Preparation Of Ceftiofur Sodium And Its Intermediates
标题:New Method For The Preparation Of Ceftiofur Sodium And Its Intermediates
摘要:本发明涉及一种制备化学式(i)中的头孢噻呋酸及其药用可接受盐(如钠盐或盐酸盐)的新方法,并提供了两种新的中间体,其化学式分别为(v)和(vi),其中x代表卤素原子,如氯或溴,R代表对甲氧基苯甲基,对硝基苯甲基或二苯甲基基团.

海关参考信息

专利信息


专利号:US-5847150-A
优先权日:1996-04-24
标题 :Solid phase and combinatorial synthesis of substituted 2-methylene-2, 3-dihydrothiazoles and of arrays of substituted 2-methylene-2, 3-dihydrothiazoles
发明人:DORWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS
摘要:A solid phase method for the synthesis of a plurality of differently substituted 2-methylenethiazoles with a wide variety of side-chain substituents as compounds of potential therapeutic interest. The 2-methylenethiazoles are prepared by acylation of a substrate-bound primary or secondary amine with cyanoacetic acid and reaction of the resulting cyanoacetamide with an isothiocyanate in the presence of a base. Alkylation with an appropriate alkyl halide under acidic conditions yields differently substituted, support-bound 2-methylene-2,3-dihydrothiazoles. These may be screened on the substrate or cleaved from the substrate and then screened in solution. The efficient synthesis of a wide variety of 2-methylenethiazoles using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiazole-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.

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-2005186197-A1
优先权日:2002-08-29
标 题:Peptide inhibitors of beta lactamases
发明人:PALZKILL TIMOTHY; HUANG WANZHI
摘要:Peptide inhibitors of β-lactamases have been identified by the synthesis of peptide arrays using synthesis SPOT technology. These peptide inhibitors of β-lactamase have activity against a broad spectrum of β-lactamases and are useful in a variety of applications.

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:WO-03059914-A1
优先权日:2002-01-15
标 题 :An improved synthesis of ceftiofur intermediate
发明人:DESHPANDE PRAMOD NARAYAN; KHADANGALE BHAUSAHEB PANDHARIN; KUMAR SURULICHAMY SENTHIL; DAS GAUTAM KUMAR
权利人:ORCHID CHEMICALS & PHARM LTD; DESHPANDE PRAMOD NARAYAN; KHADANGALE BHAUSAHEB PANDHARIN; KUMAR SURULICHAMY SENTHIL; DAS GAUTAM KUMAR
摘要:The present invention provides an improved process for the preparation of 7-amino-3-[2-(furylcarbonyl)thiomethyl]-3-cephem-4-carboxylic acid represented by formula (I) (I)by the condensation of 7-amino cephalosporanic acid (7-ACA) represented by formula (II) with furyl-2-carbonylthiol represented by formula (III) using borontrifluoride as condensing agent in an organic solvent at a temperature range of 20 DEG -50 DEG C.

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.
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主要参考文献


1: Carson C, Li XZ, Agunos A, Loest D, Chapman B, Finley R, Mehrotra M, Sherk LM, Gaumond R, Irwin R. Ceftiofur-resistant Salmonella enterica serovar Heidelberg of poultry origin - a risk profile using the Codex framework. Epidemiol Infect. 2019 Nov 4;147:e296. doi: 10.1017/S0950268819001778.
2: Reppert EJ. Evidence for the use of ceftiofur for treatment of metritis in dairy cattle. Vet Clin North Am Food Anim Pract. 2015 Mar;31(1):139-49, vii. doi: 10.1016/j.cvfa.2014.11.007. Epub 2015 Jan 9.
95:103295. doi: 10.1016/j.jevs.2020.103295. Epub 2020 Oct 12. 2(7):717-31. doi: 10.2174/1568026023393679. 4(1):83-93. 9(2):318. doi: 10.3390/microorganisms9020318.

合成参考文献


摘要:21 CFR 556.113; U.S. National Archives and Records Administration's Electronic Code of Federal Regulations. Available from, as of June 21, 2006:
摘要:Halling-Sorensen B et al; Chemosphere 36: 357-93 (1998)
摘要:O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. 13th Edition, Whitehouse Station, NJ: Merck and Co., Inc., 2001., p. 334
摘要:Franke C et al; Chemosphere 29: 1501-14 (1994)
摘要:S72 | NTUPHTW | Pharmaceutically Active Substances from National Taiwan University | DOI:10.5281/zenodo.3955664
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