CAS: 100848-70-2; 2-Methoxy-4-Methylpyridine

该化合物是属于类的有机化合物,其特点是用甲氧基组和甲基组替代了一条环,其分子式为C8H9NO,表明碳,氢,氮和氧原子的存在.该化合物一般是无色的,可粉色黄色,有独特的气味.它溶于乙醇和乙醚等有机溶剂,但由于其水分缺乏性,在水中溶解性有限. 2-甲基丙烯因其在有机合成中的应用以及作为各种药品和农用化学品生产的中间体而闻名.该混合体组的存在增强了其再活动性,使其成为化学反应中的有用建筑块.此外,它具有中度毒性,需要在处理过程中采取适当的安全防范措施.

结构式图片

相似化合物

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合成工艺路线路线简述

    2-氨基-4-甲基吡啶置于氢溴酸,溴,Sodium Nitrite体系中,化学反应生成2-甲氧基-4-甲基吡啶
    参考文献:1,3-Shifts. V. The Intermolecular Nature Of Some 1,3-Shifts
    标题:1,3-Shifts. V. The Intermolecular Nature Of Some 1,3-Shifts
    摘要:
    Doi:10.1021/ja01569A046

    专利信息


    专利号:US-2009111737-A1
    优先权日:1999-05-24
    标题:Novel antibacterial agents
    发明人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
    权利人:CHRISTENSEN BURTON G; MORAN EDMUND J; GRIFFIN JOHN H; JUDICE J KEVIN; MU YONGQI; PACE JOHN L; MAMMEN MATHAI; AGGEN JAMES
    摘要:This invention relates to novel multibinding compounds (agents) that are antibacterial agents. The multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands in their monovalent (i.e., unlinked) state have the ability to bind to a an enzyme involved in cell wall biosynthesis and metabolism, a precursor used in the synthesis of the bacterial cell wall and/or the bacterial cell surface thereby interfere with the synthesis and/or metabolism of the cell wall. In particular the multibinding compounds of the invention comprise from 2-10 ligands covalently connected by a linker or linkers, wherein each of said ligands hasn a ligand domain capable of binding to penicillin binding proteins, a transpeptidase enzyme, a substrate of a transpeptidase enzyme, a beta-lactamase enzyme, pencillinase enzyme, cephalosporinase enzyme, a transglycoslase enzyme, or a transglycosylase enzyme substrate; Preferably, the ligands are selected from the beta lactam or glycopeptide class of antibacterial agents.

    专利号:US-10253004-B2
    优先权日:2017-01-26
    标 题:Indanylaminopyrazinylcyclopropanecarboxylic acids, pharmaceutical compositions and uses thereof
    发明人:ECKHARDT MATTHIAS; WAGNER HOLGER; PETERS STEFAN
    权利人:BOEHRINGER INGELHEIM INT
    摘要:The present invention relates to compounds of formula I, n nwherein the groups R, R 1 , R 2 , R 3 , m and n are defined herein, which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2. Furthermore, the invention relates to novel intermediates, useful for the synthesis of compounds of formula I.

    专利号:US-8129411-B2
    优先权日:2005-12-30
    标题:Organic compounds
    发明人:EHARA TAKERU; GROSCHE PHILIPP; IRIE OSAMU; IWAKI YUKI; KANAZAWA TAKANORI; KAWAKAMI SHIMPEI; KONISHI KAZUHIDE; MOGI MUNETO; SUZUKI MASAKI; YOKOKAWA FUMIAKI
    权利人:EHARA TAKERU; GROSCHE PHILIPP; IRIE OSAMU; IWAKI YUKI; KANAZAWA TAKANORI; KAWAKAMI SHIMPEI; KONISHI KAZUHIDE; MOGI MUNETO; SUZUKI MASAKI; YOKOKAWA FUMIAKI; NOVARTIS AG
    摘要:The invention relates to 3,5-substituted piperidine compounds, these compounds for use in the diagnostic and therapeutic treatment of a warm-blooded animal, especially for the treatment of a disease (=disorder) that depends on activity of renin; the use of a compound of that class for the preparation of a pharmaceutical formulation for the treatment of a disease that depends on activity of renin; the use of a compound of that class in the treatment of a disease that depends on activity of renin; pharmaceutical formulations comprising a 3,5-substituted piperidine compound, and/or a method of treatment comprising administering a 3,5-substituted piperidine compound, a method for the manufacture of a 3,5-substituted piperidine compound, and novel intermediates and partial steps for its synthesis. n The compounds have the formula I′ n nwherein R1, R2, T, R3 and R4 are as defined in the specification.
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    合成参考文献


    摘要:Okumura, M., Science of Synthesis: Dearomatizations, (2026) .
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