CAS: 622-26-4; 2-(Piperidin-4-yl)Ethanol

该化合物是一种多用途的七环化合物,其特点是管子核心,在4位位置上有一个乙醇替代物.这种结构既具有基本性,又具有水利性,使其成为制药和农用化学合成中有价值的中间体.其管子元素通常用于开发生物活性分子,包括CNS定向药物,因为其有能力增强结合性和调制药用植物基因特性. 氢氧化合物组为进一步的衍生提供了一种功能处理,使得能够引入更多的药用植物或溶解组. 化合物的稳定性和定义明确的再活性特征使它成为医药化学和工业应用的可靠建筑块.

结构式图片

相似化合物

90747-17-4 89151-44-0 868849-54-1

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号5344-27-4 4-乙醇基吡啶 | CAS号28356-58-3 4-吡啶乙酸 | CAS号872850-91-4 2-(1,2,3,6-tetr... | CAS号64-19-7 冰醋酸 | CAS号147699-19-2 1-N-B°C-O-甲磺酰-羟乙基哌啶 | CAS号141047-47-4 4-(2-羟乙基)哌啶-1-苯甲醛 | CAS号194612-27-6 2-(1-((2,3-二氢苯并... | CAS号21156-84-3 2-(1-甲基哌啶-4-基)乙-1-醇 | CAS号89151-44-0 N-B°C-4-哌啶乙醇 | CAS号70724-70-8 4-(2-甲氧基乙基)哌啶 | CAS号142374-19-4 4-(2-氧代乙基)哌啶-1-羧酸叔丁酯 | CAS号122860-33-7 N-CBZ-4-哌啶甲醇(1-... | CAS号347873-67-0 4-(2-苯氧基乙基)哌啶 | CAS号100-76-5 奎宁环

合成工艺路线路线简述

    4-哌啶乙酸置于lithium Aluminium Tetrahydride体系中,用 四氢呋喃 作为反应溶剂,以62.5%的收率获得产物4-哌啶乙醇
    参考文献:具有抗血小板聚集活性的哌啶基取代5-羟色氨 酸衍生物
    标题:具有抗血小板聚集活性的哌啶基取代5-羟色氨 酸衍生物
    摘要:本发明涉及药物化学领域,具体涉及一种具有抗血小板聚集活性的哌啶基取代5-羟色氨酸衍生物(i)及其制备方法和在药学上的应用,其中r1,R2和n的定义同说明书.药效学试验证明,本发明的哌啶基取代5-羟色氨酸衍生物具有非常好抗血小板聚集活性.

    海关参考信息

    专利信息


    专利号:US-8304409-B2
    优先权日:2002-07-03
    标 题:Nitrosated nonsteroidal antiinflammatory compounds, compositions and methods of use
    发明人:EARL RICHARD A; EZAWA MAIKO; FANG XINQIN; GARVEY DAVID S; GASTON RICKY D; KHANAPURE SUBHASH P; LETTS L GORDON; LIN CHIA-EN; RANATUNGE RAMANI R; RICHARDSON STEWART K; SCHROEDER JOSEPH D; STEVENSON CHERI A; WEY SHIOW-JYI
    权利人:EARL RICHARD A; EZAWA MAIKO; FANG XINQIN; GARVEY DAVID S; GASTON RICKY D; KHANAPURE SUBHASH P; LETTS L GORDON; LIN CHIA-EN; RANATUNGE RAMANI R; RICHARDSON STEWART K; SCHROEDER JOSEPH D; STEVENSON CHERI A; WEY SHIOW-JYI; NICOX SA
    摘要:The invention describes novel nitrosated nonsteroidal antiinflammatory drugs (NSAIDs) and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated NSAID, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one nitrosated NSAID, and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one nitrosated NSAID, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating inflammation, pain and fever; for treating gastrointestinal disorders; for facilitating wound healing; for treating and/or preventing gastrointestinal, renal and/or respiratory toxicities resulting from the use of nonsteroidal antiinflammatory compounds; for treating inflammatory disease states and/or disorders; and for treating and/or preventing ophthalmic diseases and/or disorders.

    专利号:US-6593347-B2
    优先权日:1998-10-30
    标题 :Nitrosated and nitrosylated nonsteroidal antiinflammatory compounds, compositions and methods of use
    发明人:BANDARAGE UPUL K; DONG QING; FANG XINQIN; GARVEY DAVID S; MERCER GREGORY J; RICHARDSON STEWART K; SCHROEDER JOSEPH D; WANG TIANSHENG
    权利人:NITROMED INC
    摘要:The present invention describes novel nitrosated and/or nitrosylated nonsteroidal antiinflammatory compounds, and novel compositions comprising at least one nitrosated and/or nitrosylated nonsteroidal antiinflammatory compound, and, optionally, at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase. The present invention also provides methods for treating, preventing and/or reducing inflammation, pain, and fever; decreasing or reversing the gastrointestinal, renal and other toxicities resulting from the use of nonsteroidal antiinflammatory drugs; treating and/or preventing gastrointestinal disorders; treating inflammatory disease states and disorders; and treating and/or preventing ophthalmic diseases or disorders.

    专利号:US-10730037-B2
    优先权日:2015-12-25
    标题:Compound and method for manufacturing organic material
    发明人:MIYAZAWA TAKASHI; SAKAGUCHI KEN-ICHI
    权利人:TOYO GOSEI CO LTD
    摘要:Synthesis of organic compounds that has chirality is an important technique in the fields of pharmaceuticals, agrichemicals, health foods and the like. However, raw materials of a catalyst used for the synthesis of such compounds are expensive, and the synthesis needs many steps, so that it is difficult to reduce the cost. Linking a catalyst center to a polymer chain or a resin through an organic group enables to use the catalyst repeatedly and produce a chiral compound at low cost.

    专利号:US-9562037-B2
    优先权日:2014-02-26
    标题:Synthesis and use of amine-containing flavonoids as potent anti-leishmanial agents
    发明人:CHOW LARRY MING-CHEUNG; CHAN WILLIAM TAK HANG; CHAN KIN-FAI; WONG IRIS LAI KING; KAN WING-YIU
    权利人:UNIV HONG KONG POLYTECHNIC
    摘要:The present invention relates to novel series of amine-containing flavonoids and compositions containing the compounds, as well as the synthesis and the use of the same. The invention also relates to methods of treatment and prevention of diseases, in particular, parasitic infections including Leishmaniasis, comprising administration of the compounds.

    专利号:US-10111854-B2
    优先权日:2014-02-26
    标题 :Synthesis and use of amine-containing flavonoids as potent anti-leishmanial agents
    发明人:CHOW LARRY MING-CHEUNG; Chan Tak Hang William; CHAN KIN-FAI; WONG IRIS LAI KING; KAN WING-YIU
    权利人:UNIV HONG KONG POLYTECHNIC
    摘要:The present invention relates to novel series of amine-containing flavonoids and compositions containing the compounds, as well as the synthesis and the use of the same. The invention also relates to methods of treatment and prevention of diseases, in particular, parasitic infections including Leishmaniasis, comprising administration of the compounds.

    专利号:US-5939392-A
    优先权日:1993-06-03
    标 题 :Method of thrombin inhibition
    发明人:ANTONSSON KARL THOMAS; BYLUND RUTH ELVY; GUSTAFSSON NILS DAVID; NILSSON NILS OLOV INGEMAR
    权利人:ASTRA AB
    摘要:The invention relates to new competitive tripeptide inhibitors of trypsin-like serine proteases, their synthesis, pharmaceutical compositions containing the compounds as active ingredients, and the use of the compounds as thrombin inhibitors, anticoagulants and antiinflammatory inhibitors for prophylaxis and treatment of related diseases.
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    合成参考文献


    摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
    摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
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