CAS: 13726-14-2; 4-Chloro-3-Methoxyaniline

该化合物是有机化合物,其特点是有氯和甲氧混合物组,附于一个阴性结构,其副位置为氯替代物,与苯环上的氨基组相比,其元位置为甲氧基组,该化合物一般为固体,以其黄色至褐色的颜色而闻名;乙醇和丙酮等有机溶剂溶解,但由于其缺水芳香结构,其溶解性有限. 4-Chrolodo-3-methoxyaniline由于具有活性,而且有能力进行各种化学变异,因此经常用于染色,色和制药合成.此外,该化合物可能展示生物活动,使其对药用化学感兴趣.适当的处理和安全防范是必要的,因为若吸入或浸入,可能会对健康造成危害,因此应当按照相关的安全准则加以管理.

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1009-36-5 113206-03-4 98446-49-2

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合成工艺路线路线简述

    📜2,5-二氯苯甲醚置于iron(III) Nitrate Nonahydrate,氨,Sodium体系中,用 正己烷 用作溶剂,化学反应 2.0H,以99%的收率获得3-甲氧基-4-氯苯胺
    参考文献:7-(2-苯氧基乙氧基)-4(1H)-喹诺酮类的合成,抗疟活性及构效关系
    标题:7-(2-苯氧基乙氧基)-4(1H)-喹诺酮类的合成,抗疟活性及构效关系
    摘要:Ici 56,780 ( 5 ) 在啮齿动物疟疾模型中显示出因果预防和血液分裂活性(ed 50 = 0.05 Mg/kg),但在感染伯氏疟原虫的小鼠中迅速获得了寄生虫学抗性.在此,我们描述了针对多药耐药恶性疟原虫的 Ec 50低至 0.15 Nm的5类似物的合成.通过在 7-(2-Phenoxyethoxy)-4(1 H )-Quinolone 核心的 3 位引入邻位取代的芳基部分,实现了对 Atovaquone 的低交叉阻力指数 (Ri) 的最佳活性.
    Doi:10.1021/jm200718M

    海关参考信息

    专利信息


    专利号:US-2024182421-A1
    优先权日:2021-03-19
    标题 :Synthesis of endochin-like quinolones
    发明人:RISCOE MICHAEL K; NILSEN AARON; JIN HAIHONG; POU SOVITJ; WINTER ROLF W; DODEAN ROZALIA ANA; LIEBMAN KATHERINE M
    权利人:UNIV OREGON HEALTH & SCIENCE; US GOV VETERANS AFFAIRS
    摘要:Described herein are new synthetic routes for production of Endochin-Like Quinolone (ELQ) compounds. Synthetic routes to 3-substituted 4(1H)-quinolones are presented that are amenable to industrial scale preparation. One herein presented approach is relatively short, does not require palladium, and involves no chromatographic separation. A second herein presented approach is similarly relatively short, does not require palladium, involves no chromatographic separation, and also avoids high vacuum distillation. Additionally, both approaches require no protecting group chemistry because the insoluble 4(1H)-quinolone is not formed until the final reaction step.

    专利号:EP-1836163-B1
    优先权日:2004-12-23
    标题 :Pyrrolidine derivatives for the treatment of a disease depending on the activity of renin
    发明人:BREITENSTEIN WERNER; COTTENS SYLVAIN; EHRHARDT CLAUS; JACOBY EDGAR; LORTHIOIS EDWIGE LILIANE JEANNE; MAIBAUM JUERGEN KLAUS; OSTERMANN NILS; SELLNER HOLGER; SIMIC OLIVER
    权利人:NOVARTIS AG
    摘要:Novel 3-mono-, 3,4-di- and 3,4,4,-tri-substituted pyrrolidine 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 inappropriate 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 inappropriate activity of renin; the use of a compound of that class in the treatment of a disease that depends on inappropriate activity of renin; pharmaceutical formulations comprising a said substituted pyrrolidine compound, and/or a method of treatment comprising administering a said substituted pyrrolidine compound, a method for the manufacture of said substituted pyrrolidine compounds, and novel intermediates and partial steps for their synthesis are described. The substituted pyrrolidine compounds are especially of the formula I wherein the substituents are as described in the specification.

    专利号:WO-9509156-A1
    优先权日:1993-09-27
    标 题 :Processes and intermediates for the enantiospecific synthesis of benzo(d)naphth(2.1-b)azepines

    专利号:WO-2022197979-A1
    优先权日:2021-03-19
    标题:Synthesis of endochin-like quinolones

    专利号:EP-4308109-A1
    优先权日:2021-03-19
    标 题:Synthesis of endochin-like quinolones

    专利号:CN-117042768-A
    优先权日:2021-03-19
    标题:Synthesis of doxine-like quinolones

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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


    参考文献:10.1055/s-0040-1720912
    摘要:Scalable Synthesis of ELQ-300. Synfacts. 2021 Oct 19;17(11):1186. doi: 10.1055/s-0040-1720912.
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