CAS: 675-21-8; 5-Fluoropyrimidine

该化合物是一种七环有机化合物,其特征是五点方位以氟原子替代的环,其分子式为C4H4FNF2,其分子重量约为100.08克/摩尔,该化合物一般无色可粉黄色液体或固体,视其形式和纯度而定. 5-Fluoropyrimidine因其在各种药物合成中扮演中间角色而闻名,特别是在抗病毒剂和抗癌症剂的研制中.它显示出氟化合物的典型特性,例如由于存在电阴性增加和因电阴性氟素的存在而改变的再活性.该化合物还关心生物化学研究,特别是与核酸新陈代谢和某些酶抑制有关的研究.在处理5-Fluoropyimidine时,应当采取安全防范措施,因为它可能构成健康风险,包括毒性和潜在致癌影响.

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54376-50-0 947533-45-1 62802-42-0

上下游产品

CAS号210169-03-2 2,4,6-tribromo-... | CAS号4595-59-9 5-溴嘧啶 | CAS号128229-03-8 (2,3,3-Trifluor... | CAS号6313-33-3 甲脒盐酸盐 | CAS号109-89-7 二乙胺

合成工艺路线路线简述

    📜2,4,6-三溴-5-氟嘧啶置于palladium On Activated Charcoal 三正丁胺,氢气体系中,用 二氯甲烷 作为反应溶剂,化学反应 24.0H,以100%的收率获得产物5-氟嘧啶
    参考文献:Chambers,Richard D.; Hall,Christopher W.; Hutchinson,John,Journal Of The Chemical Society. Perkin Transactions I,1998,# 10,P. 1705-1713
    标题:Chambers,Richard D.; Hall,Christopher W.; Hutchinson,John,Journal Of The Chemical Society. Perkin Transactions I,1998,# 10,P. 1705-1713

    专利信息


    专利号:US-5663323-A
    优先权日:1993-02-23
    标题 :Synthesis of 4-alkoxy-5-fluoro-2'-deoxyuridine and its incorporation into oligonocleotides
    发明人:SOWERS LAWRENCE C
    权利人:HOPE CITY
    摘要:A synthesis of 5-fluoro-2'-ideoxycytidine, of oligonucleotides containing 5-fluoro-2'-deoxycytidine and of certain novel 4-alkoxy-5-fluoro-2'-deoxyuridines is disclosed. These 4-alkoxy compounds are useful intermediates for the preparation of other 4-substituted, 5-fluoro pyrimidine deoxynucleosides, and spontaneously hydrolyze in target cells to form FdU and derivatives thereof.

    专利号:US-9573873-B2
    优先权日:2014-06-03
    标题:Catalytic method for dibenzocycloheptane synthesis and allocolchicinoid synthesis
    发明人:GREEN JAMES; MEHDI MARIAM; DJURDJEVIC SINISA
    权利人:UNIV OF WINDSOR
    摘要:In a non-limiting embodiment, there is provided a compound of formula (I), which may permit for a method or use in treating or preventing a cancer, such as pancreatic cancer or leukemia. In one embodiment, there is also provide a method of preparing a compound of formula (Ia), the method including conducting a cyclization reaction of a compound of formula (III) to obtain a compound of formula (IV), wherein conducting the cyclization reaction comprises conducting a Michael reaction in the presence of a Lewis acid.

    专利号:US-5110929-A
    优先权日:1986-08-07
    标题 :Process for the preparation of N-alkylated quaternary nitrogen containing aromatic heterocycles
    发明人:PARADIES HENRICH H
    权利人:MEDICE CHAM PHARM FABRIK PUTTE
    摘要:The synthesis of 4-, 4-(1,1)-and 3,5-substituted N-alkyl-pyridinium salts as well as of 2-carboxamide substituted N(1,4)diazinium compounds are described. The N-surfactants obtained have a small critical micelle concentration (CMC) of 10-5 -10-7 Mol/Liter. These surfactants produce micells of different size and form depending on the nature of the anions. 4-(1,1)-substituted and 3,5-substituted N-alkyl-pyridinium components are capable of forming vesicles in equeous solutions of different forms and sizes. The N-surfactants synthesized can be used as pharmaceuticals.

    专利号:US-8673885-B1
    优先权日:2010-07-25
    标 题 :Compounds for the protection of sulfur containing linkers in nucleic acid synthesis
    发明人:DUFF ROBERT
    权利人:DUFF ROBERT
    摘要:Aromatic and alkyl thiocarbonates with and without a neighboring group that participates in the hydrolysis of a thiocarbonate are described. The aromatic or alkyl thiocarbonates can be used for the protection of sulfur during oligonucleotide synthesis. Their facile processes of manufacture and methods of using the same are provided.

    专利号:US-2017355648-A1
    优先权日:2016-04-26
    标题 :Synthesis of meta-substituted [18f]-3-fluoro-4-aminopyridines by direct radiofluorination of pyridine n-oxides

    专利号:US-12054512-B2
    优先权日:2017-11-10
    标 题 :Sting modulator compounds, and methods of making and using
    发明人:VYSKOCIL STEPAN; CIAVARRI JEFFREY; CULLIS COURTNEY; ENGLAND DYLAN BRADLEY; GOULD ALEXANDRA E; GREENSPAN PAUL; HU YONGBO; LANGSTON STEVEN; LI GANG; MIZUTANI HIROTAKE; OKANIWA MASANORI
    权利人:TAKEDA PHARMACEUTICALS CO
    摘要:The present disclosure provides STING modulators/agonists, and methods of synthesis and methods for using for the prophylaxis or treatment of cancer and other STING-related diseases.The present disclosure relates to a compound represented by the Formula (I):wherein each symbol is as defined in the description, or a pharmaceutically acceptable salt thereof.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Wang, X.; Hu, J., Science of Synthesis: Modern Strategies in Organofluorine Chemistry, (2025) 2.
    参考文献:10.1007/s101200050041
    摘要:Suda Y, Kuwashima Y, Tanaka Y, Uchida K, Sakamoto H, Hashiguchi Y, Sekine T. Expression of thymidylate synthase and thymidine phosphorylase in recurrence and survival rates of advanced gastric cancer. Gastric Cancer. 1999 Nov;2(3):165–72. doi: 10.1007/s101200050041.
    参考文献:10.1186/s12885-018-4405-7
    摘要:Healy MA, Morris AM, Abrahamse P, Ward KC, Kato I, Veenstra CM. The accuracy of chemotherapy ascertainment among colorectal cancer patients in the surveillance, epidemiology, and end results registry program. BMC Cancer. 2018 Apr 27;18(1):481.
    参考文献:10.1007/s40520-018-0956-3
    摘要:Zorzoli E, Pica F, Masetti G, Franco E, Volpi A, Gabutti G. Herpes zoster in frail elderly patients: prevalence, impact, management, and preventive strategies. Aging Clinical and Experimental Research. 2018 May 02;30(7):693–702. doi: 10.1007/s40520-018-0956-3.
    参考文献:10.1007/bf00689968
    摘要:Prezioso JA, Wang N, Bloomer WD. Thymidylate synthase as a target enzyme for the melanoma-specific toxicity of 4-S-cysteaminylphenol and N-acetyl-4-S-cysteaminylphenol. Cancer Chemother Pharmacol. 1992;30(5):394–400. doi: 10.1007/bf00689968.
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