CAS: 22614-69-3; 8-Methoxyquinolin-2(1H)-One

该化合物是属于五醇类的化学化合物,属于双环芳香化合物,该物质在8位置上具有甲氧基(-OCH3),在2位置的奎宁环上具有碳基(C=O),具有潜在生物活动的特点,包括抗微生物和抗沙素特性,因此对医药化学感兴趣.该化合物一般呈现黄色至褐色的黄色至褐色,在有机溶剂中可溶解.其分子结构有助于其再活动以及与各种生物目标的相互作用.此外,8-甲氧基苯基苯丙胺-2(1H)-one可以参与各种化学反应,例如核乐类替代和循环,这些在合成有机化学中很有价值.在处理和使用时,应参考安全数据,因为与任何化学物质一样,确保采取适当的防范措施.

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合成工艺路线路线简述

    📜8-甲氧基喹啉氮氧化物置于1,8-Dimethoxy-10-Phenyl-9-(O-Tolyl)Acridin-10-Ium Chloride体系中,用 二甲基亚砜 用作溶剂,化学反应 8.0H,以94%的收率获得8-甲氧基喹啉-2-酮
    参考文献:从喹啉n-氧化物中高效可见光介导的喹啉-2(1H)-酮的合成
    标题:从喹啉n-氧化物中高效可见光介导的喹啉-2(1H)-酮的合成
    摘要:Quinolin-2( 1H )-Ones 是一类重要的化合物,因为它们普遍存在于天然产物和药理学上有用的化合物中.在这里,我们提出了一种非常规且迄今为止未知的光催化方法,从容易获得的喹啉-N-氧化物合成它们.这种不含试剂的高原子经济性光催化方法具有低催化剂负载,高产率和无不良副产物,为迄今为止报道的所有常规合成提供了一种更有效的绿色替代方案.该方法的稳健性已成功证明,可轻松扩展到克级.
    Doi:10.1039/d1Gc01460A

    海关参考信息

    专利信息


    专利号:US-9302992-B2
    优先权日:2013-04-02
    标 题:Multifunctional quinoline derivatives as anti-neurodegenerative agents
    发明人:CHERN JI-WANG; HUANG CHEN-WEI; CHANG PEI-TEH; TALEKAR RAHUL SUBHASH
    权利人:ANNJI PHARM CO LTD
    摘要:Novel quinoline derivatives are disclosed. Also disclosed are synthesis and use thereof for treating neurodegenerative diseases. In one aspect, the invention relates to a compound of Formula (I) or a pharmaceutically acceptable salt thereof: n n(I) whereinn R 1 is hydrogen, (C 1 -C 8 )alkyl, (C 1 -C 8 )alkylene(C 3 -C 8 )cycloalkyl, (C 1 -C 8 )haloalkyl, or (C 1 -C 8 )alkylene(C 6 -C 20 )aryl; R 2 is hydrogen or halogen; R 3 is hydrogen, halogen, (C 1 -C 8 )alkyl, or (C 1 -C 8 )alkoxy; R 4 is hydrogen, halogen, (C 1 -C 8 )alkyl, (C 1 -C 8 )alkoxy, or (C 1 -C 8 )haloalkyl; R 5 is hydrogen or (C 1 -C 20 )alkanol; R 6 is hydrogen; and R 7 is (C 1 -C 20 )alkanol, (C 1 -C 8 )alkylene (C 3 -C 8 )heterocyclyl(C 1 -C 20 )alkanol, (C 1 -C 8 )alkylene (C 3 -C 8 )heterocyclyl(C 1 -C 20 )alkyl, (C 1 -C 8 )alkylene(C 1 -C 6 )alkylamino(C 1 -C 6 )alkynyl, (C 1 -C 8 )alkyleneamino(C 1 -C 20 )alkanol, or (C 1 -C 8 )alkyleneamino(C 1 -C 20 )alkanol(C 1 -C 8 )alkylene substituted (C 3 -C 20 )heteroaryl;n n(II) or wherein:n R 1 , R 2 , R 3 , R 4 and R 6 are each defined in (I) above; R 5 is (C 1 -C 20 )alkanol; and R 7 is hydrogen, (C 1 -C 20 )alkanol, (C 1 -C 8 )alkylene (C 3 -C 8 )heterocyclyl(C 1 -C 20 )alkanol, (C 1 -C 8 )alkylene (C 3 -C 8 )heterocyclyl(C 1 -C 20 )alkyl, (C 1 -C 8 )alkylene(C 1 -C 6 )alkylamino(C 1 -C 6 )alkynyl, (C 1 -C 8 )alkyleneamino(C 1 -C 20 )alkanol, or (C 1 -C 8 )alkyleneamino(C 1 -C 20 )alkanol(C 1 -C 8 )alkylene substituted (C 3 -C 20 )heteroaryl.

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    合成参考文献


    参考文献:10.1007/s101560200019
    摘要:Miyashita N, Fukano H, Yoshida K, Niki Y, Matsushima T. In-vitro activity of moxifloxacin and other fluoroquinolones against Chlamydia species. J Infect Chemother. 2002 Mar;8(1):115–7. doi: 10.1007/s101560200019.
    参考文献:10.2165/00003495-199958002-00001
    摘要:Andriole VT. The future of the quinolones. Drugs. 1999;58 Suppl 2():1–5. doi: 10.2165/00003495-199958002-00001.
    参考文献:10.2165/00003495-199958002-00005
    摘要:Eliopoulos GM. Activity of newer fluoroquinolones in vitro against gram-positive bacteria. Drugs. 1999;58 Suppl 2():23–8. doi: 10.2165/00003495-199958002-00005.
    参考文献:10.2165/00003495-199958002-00006
    摘要:Turnidge J. Pharmacokinetics and pharmacodynamics of fluoroquinolones. Drugs. 1999;58 Suppl 2():29–36. doi: 10.2165/00003495-199958002-00006.
    参考文献:10.2165/00003495-199958002-00008
    摘要:Jafri HS, McCracken GH. Fluoroquinolones in paediatrics. Drugs. 1999;58 Suppl 2():43–8. doi: 10.2165/00003495-199958002-00008.
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