CAS: 41037-26-7; 6-Methoxy-4-Methylquinoline

该化合物是一种环环环生物化合物,在6位置以甲氧基组替代一个奎诺基,在4位置以甲氧基组替代一个甲基组,这种结构具有独特的电子和消毒特性,使其成为制药和农用化学合成中有价值的中间体,其甲氧基和甲基替代体在交叉反应中增强了回动性和选择性,而quinoline脚架则有助于协调化学和材料科学应用. 复合体在标准条件下具有稳定性,与一系列合成变异相兼容,为生物活性分子和功能材料的开发提供了多种用途.

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5429-01-6 6238-12-6 1078-28-0

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上下游产品

dihydroquinidine dihydroquinine Quinine 1.3-butanediol6-methoxy-4-styryl-quinoline 1,1,1-trichloro-3-(6-methoxy-[4]quinolyl)-propan-2-ol 6-methoxy-4-methyl-2-phenylquinoline N,N-dimethyl-aniline4-[2-(6-methoxy-quinolin-4-yl)-vinyl]-N,N-dimethyl-aniline

合成工艺路线路线简述

    📜乙酰基乙酰对甲氧基苯胺置于硫酸,三氯氧磷,溶剂黄146,锌体系中,用72%的收率获得产物6-甲氧基-4-甲基喹啉水合物
    参考文献:立体控制奎宁和奎尼丁的合成
    标题:立体控制奎宁和奎尼丁的合成
    摘要:由环戊烯单乙酸酯制备二取代的环戊烯,并通过烯烃部分的氧化裂解,然后形成哌啶环,将其转移到二取代的哌啶中.然后将哌啶在侧链上与喹啉部分缩合,得到奎宁的烯烃前体.最后,烯烃通过相应的环氧化物转化为奎宁.奎尼丁以类似方式合成.
    DOI:10.1016/j.Tetlet.2004.03.085

    海关参考信息

    专利信息


    专利号:US-7692016-B2
    优先权日:2005-11-25
    标 题 :Process for the synthesis of quinoline derivatives
    发明人:MADUGULA SREE RAMA MURTY; THALLAPELLY SWAMY; BANDARUPALLY JYOTHIRMAI; YADAV JHILLU SINGH
    权利人:COUNCIL SCIENT IND RES
    摘要:The present invention provides an improved process for the synthesis of quinoline derivatives. More particularly the present invention provides an improved and economical process for the synthesis of quinoline derivatives by the reaction of aniline/substituted anilines using two different catalysts, ferric chloride and zinc chloride in a one-pot set up reaction.

    专利号:US-3989691-A
    优先权日:1973-01-05
    标 题 :Preparation of cinchona alkaloid intermediates
    发明人:TAYLOR EDWARD C; MARTIN STEPHEN F
    权利人:UNIV PRINCETON
    摘要:4-[3-(3-vinyl-1-acetyl-4-piperidyl)-1-propenyl]-6-methoxyquinoline, the corresponding epoxide and related compounds, useful in the synthesis of Cinchona alkaloids, are prepared by introducing an ylid group in the 4-position of a suitably substituted quinoline and reacting this ylid with an N-acetyl-4-piperidineacetaldehyde.

    专利号:US-2007123708-A1
    优先权日:2005-11-25
    标 题:Process for the synthesis of quinoline derivatives

    专利号:WO-2007060685-A1
    优先权日:2005-11-25
    标 题:An improved process for the synthesis of quinoline derivatives

    专利号:US-7897774-B2
    优先权日:2005-03-03
    标题:Cyclic compound having quinolylalkylthio group
    发明人:KAWASHIMA KENJI; HONDA TAKAHIRO; TAJIMA HISASHI; OKAMOTO KAZUYOSHI; YAMAMOTO MINORU
    权利人:SANTEN PHARMACEUTICAL CO LTD
    摘要:The present invention relates to a synthesis study of novel cyclic compounds having a quinolylalkylthio group represented by the formula (1), and pharmacological actions of the compounds. n nIn the formula, the ring X represents:n n nwhich may have halogen and/or alkyl; R 1 and R 2 independently represent hydrogen, alkyl, cycloalkyl, aryl or a (non) aromatic heterocycle; R 3 represents qinolyl; A represents sulfur, sulfinyl or sulfonyl; and B represents alkylene.

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    合成参考文献


    参考文献:10.1055/s-0029-1218601
    摘要:Peters R, Jautze S. Catalytic Asymmetric Michael Additions of α-Cyanoacetates. Synthesis. 2009 Dec 11;2010(03):365–88. doi: 10.1055/s-0029-1218601.
    参考文献:10.1055/s-0036-1590958
    摘要:Chen L. Recent Advances in the Catalytic Asymmetric Construction of Phosphorus-Substituted Quaternary Carbon Stereocenters. Synthesis. 2017 Nov 27;50(03):440–69. doi: 10.1055/s-0036-1590958.
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