CAS: 50741-46-3; Ethyl Quinoline-3-Carboxylate

该化合物是一种多用途有机化合物,在3点处经过肾上核作用的测试,是制药和农用化学合成中有价值的中间体,特别是用于建造异环框架.乙酯组增加了溶性和再活性,有利于进一步的功能化.在温和条件下,乙基酯组的稳定性使其适合多种反应,包括核生殖替代和循环.quinoydy有助于其开发生物活性分子,如抗微生物或抗图象剂的效用.该组的特点是高度纯度和一贯性,确保研究和工业应用的可靠性.建议适当处理和储存以保持其完整性.

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相似化合物

13669-42-6 6480-68-8 13669-51-7

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ECHA物质C&L通报

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CAS号195719-66-5 potassium quino... | CAS号64-17-5 乙醇 | CAS号451491-93-3 ethyl (E)-2-(((... | CAS号10601-80-6 3,3-二乙氧基丙酸乙酯 | CAS号552-89-6 邻硝基苯甲醛 | CAS号6480-68-8 喹啉-3-羧酸 | CAS号75-03-6 碘乙烷 | CAS号73396-97-1 2-iodo-N-(2-car... | CAS号100-52-7 苯甲醛 | CAS号13669-51-7 喹啉-3-基甲醇 | CAS号13669-42-6 3-喹啉甲醛 | CAS号15785-08-7 2-甲基喹啉-3-羧酸乙酯 | CAS号67752-37-8 1,2,3,4-四氢喹啉-3-羧酸乙酯 | CAS号4945-38-4 Furo[3,4-b]quin... | CAS号59282-61-0 喹啉-3-甲酰肼

合成工艺路线路线简述

    📜Ethyl 3-Acetoxy-3-(2-Azidophenyl)-2-Methylenepropanoate置于三苯基膦,Sodium Nitrite体系中,用 N,N-二甲基甲酰胺,甲苯 作为反应溶剂,化学反应 15.0H,反应生成 3-喹啉羧酸乙酯
    参考文献:使用morita-baylis-hillman 2-叠氮基苯甲醛的乙酸酯合成2-烷氧基-3-氰基甲基喹啉和烷基喹啉-3-羧酸盐
    标题:使用morita-baylis-hillman 2-叠氮基苯甲醛的乙酸酯合成2-烷氧基-3-氰基甲基喹啉和烷基喹啉-3-羧酸盐
    摘要:一种简单的方法,可使用亚氨基膦烷介导的3-(2-叠氮基苯基)-2-氰基甲基丙酸酯和3-(2-叠氮基苯基)-2-亚胺基膦酸酯环化反应合成几种2-烷氧基-3-氰基甲基喹啉和烷基喹啉3-羧酸酯. ‐硝基甲基丙烯酸酯已开发出来.这些化合物分别是使用氰化钾或亚硝酸钠,分别从2-叠氮基苯甲醛的森田-贝利斯-希尔曼乙酸盐中获得的.j.杂环化学.(2011)
    DOI:10.1002/jhet.667

    海关参考信息

    专利信息


    专利号:WO-2015198349-A1
    优先权日:2014-06-25
    标 题 :A one pot synthesis of 3-substituted quinoline carboxylates and its derivatives
    发明人:GADAKH SUNITA KHANDERAO; SUDALAI ARUMUGAM
    权利人:COUNCIL SCIENT IND RES
    摘要:The present invention provides a one pot, simple, cost effective and industrially feasible catalytic synthesis of quinolines or substituted quinolines from anilines with yield >80% yield. The present invention also discloses a process for the synthesis of oxolinic acid using quinolines with yield > 45%.

    专利号:US-4021429-A
    优先权日:1975-07-24
    标 题 :Synthesis of ethylenically unsaturated compounds from esters or amides
    发明人:SCHROCK RICHARD ROYCE
    权利人:DU PONT
    摘要:Certain hydrocarbylidene-niobium or -tantalum complexes react with esters or N,N-disubstituted amides to produce ethylenically unsaturated compounds. Exemplary is the reaction of trineopentyl(neopentylidene)tantalum with ethyl acetate to produce 2-ethoxy-4,4-dimethyl-2-pentene:

    专利号:US-10227355-B2
    优先权日:2015-02-03
    标题:Quinoline derivatives and preparation thereof
    发明人:BALARAMAN EKAMBARAM; MIDYA SIBA PRASAD; JAISWAL GARIMA
    权利人:COUNCIL SCIENT IND RES
    摘要:The patent discloses novel quinoline derivatives of formula (I), (Formula should be inserted here) and process for preparing the same. The compounds of formula (I) can be further used for the synthesis of Inhibitors like Kinase Tyrosine Inhibitors.

    专利号:CN-101418005-B
    优先权日:2008-12-22
    标 题:A new method for the synthesis of prulifloxacin

    专利号:CN-101418005-A
    优先权日:2008-12-22
    标题:A new method for the synthesis of prulifloxacin

    专利号:US-2008200475-A1
    优先权日:2005-03-28
    标题:4-Piperazinothieno[2,3-D] Pyrimidine Compounds As Platelet Aggregation Inhibitors
    发明人:ENNIS MICHAEL DALTON; KORTUM STEVEN WADE; TENBRINK RUTH ELIZABETH
    权利人:PFIZER
    摘要:Compounds and pharmaceutically acceptable salts of the compounds are disclosed, wherein the compounds have the structure of Formula I: (I) wherein A 1 , A 2 , A 3 , A 4 , A 5 , A 6 , A 7 , A 8 , X 4 , X 6 , R 2a , R x , R 4 , R 5 , and R 6 are as defined in the detailed description of the invention. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

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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


    摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 243.
    摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 312.
    摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 353.
    摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 379.
    摘要:Sharma, U.; Kumar, R.; Gupta, S. S.; Chandra, D., Science of Synthesis Knowledge Updates, (2022) 2, 315.
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