CAS: 52764-11-1; 2,6-Dichloropyridin-3-Ol

该化合物是一种有机化合物,其特点是其环,在2和6个位置上被两氯原子所取代,在3个位置上被氢氧基环取代,该化合物一般是白到光黄色固体,由于存在氢氧基化合物,在水和酒精等极溶剂中可以溶解,显示出氯化化合物和的典型特性,包括潜在的生物活动. 2,6-二氯-3-基醇经常在农业中作为除草剂和杀真剂的应用以及各种药品和农用化学合成中被研究,其分子结构有助于其再活性和与生物系统的互动,使其在环境化学和药用化学中都受到关注.安全数据表明,与许多氯化化合物一样,应谨慎地处理它,因为其潜在的毒性和环境影响.

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6636-78-8 41288-96-4 1196157-47-7

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CAS号148493-34-9 2,6-二氯-3-吡啶硼酸 | CAS号6636-78-8 2-氯-3-羟基吡啶 | CAS号2402-78-0 2,6-二氯吡啶 | CAS号1214340-74-5 2,6-二氯-3-甲氧基吡啶 | CAS号62804-93-7 ethyl 2-(2,6-di...

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    📜2,6-二氯吡啶置于正丁基锂,双氧水,二异丙胺体系中,用 四氢呋喃,正己烷,二氯甲烷,水 作为反应溶剂,化学反应 21.0H,反应生成 2,6-二氯-3-羟基吡啶
    参考文献:Efficient Synthesis Of Halohydroxypyridines By Hydroxydeboronation
    标题:Efficient Synthesis Of Halohydroxypyridines By Hydroxydeboronation
    摘要:This Paper Describes A General Method For The Synthesis Of Halohydroxypyridines From Novel Halopyridinylboronic Acids And Esters Recently Described By Some Of Us. Halopyridinylboronic Acids And Esters Have Been Efficiently Hydroxydeboronated Under Mild Conditions By Employing Hydrogen Peroxide Or Meta-Chloroperbenzoic Acid. These Hydroxylations Take Place Regioselectively,Without Other Oxidation (N-Oxide Formation). (C) 2004 Elsevier Ltd. All Rights Reserved.
    DOI:10.1016/j.Tet.2004.12.006

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    专利信息


    专利号:US-9265773-B2
    优先权日:2011-09-08
    标题 :Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases
    发明人:MCCOMAS CASEY C; LIVERTON NIGEL J; HABERMANN JOERG; KOCH UWE; NARJES FRANK; LI PENG; PENG XUANJIA; SOLL RICHARD; WU HAO; PALANI ANANDAN; HE SHUWEN; DAI XING; LIU HONG; LAI ZHONG; LONDON CLARE; XIAO DONG; ZORN NICOLAS; NARGUND RAVI
    权利人:MCCOMAS CASEY C; LIVERTON NIGEL J; HABERMANN JOERG; KOCH UWE; NARJES FRANK; LI PENG; PENG XUANJIA; SOLL RICHARD; WU HAO; PALANI ANANDAN; HE SHUWEN; DAI XING; LIU HONG; LAI ZHONG; LONDON CLARE; XIAO DONG; ZORN NICOLAS; NARGUND RAVI; MERCK SHARP & DOHME; MSD ITALIA SRL
    摘要:The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

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    主要参考文献

    参考标题:Tetracyclic Heterocycle Compounds And Methods Of Use Thereof For The Treatment Of Viral Diseases
    摘要:The Present Invention Relates To Compounds Of Formula (I) That Are Useful As Hepatitis C Virus (Hcv) Ns5B Polymerase Inhibitors, The Synthesis Of Such Compounds, And The Use Of Such Compounds For Inhibiting Hcv Ns5B Polymerase Activity, For Treating Or Preventing Hcv Infections And For Inhibiting Hcv Viral Replication And/or Viral Production In A Cell-Based System.

    合成参考文献


    参考文献:10.1007/978-3-319-04346-3_13
    摘要:Röschenthaler G, Kazakova O. Chemistry of α-Fluorinated Ethers- and Thioethers-Containing Heterocycles. 2014. In: Fluorine in Heterocyclic Chemistry Volume 1. : Springer International Publishing; 2014.
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