CAS: 1268521-85-2; Trans-3-Hydroxycyclobutanecarboxylic Acid

该化合物是一种具有氢氧基组和转基因功能的有机环丁烷衍生物,该化合物是有机合成的多功能构件,特别是用于制备药用活分子和精细化学物.其硬性环丁烷环和立体化学纯度为研究结构活动关系和设计受限制的类似物提供了宝贵价值.这种跨式配置加强了稳定性和影响再活动,在不对称合成和药用化学应用方面提供了优势.高纯度和定义明确的立体化学确保了研究和工业工艺的再生性.适合用于浸泡性微生物,催化剂和生物活性化合物开发.

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63485-51-8 552849-33-9 4958-02-5

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C&L通报

合成工艺路线路线简述

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    专利信息


    专利号:US-9676783-B2
    优先权日:2008-10-22
    标 题:Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds
    发明人:HAAS JULIA; ANDREWS STEVEN W; JIANG YUTONG; ZHANG GAN
    权利人:ARRAY BIOPHARMA INC
    摘要:Compounds useful in the synthesis of compounds for treating pain, cancer, inflammation, neurodegenerative disease or Typanosoma cruzi infection in a mammal.

    专利号:DK-2725028-T3
    优先权日:2008-10-22
    标题:Substituted pyrazolo [1,5-a] pyrimidine compounds as intermediates in the synthesis of kinase inhibitors TRK

    专利号:EP-2725028-A1
    优先权日:2008-10-22
    标题 :Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors

    专利号:EP-2725028-B1
    优先权日:2008-10-22
    标题 :Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors

    专利号:HU-E030413-T2
    优先权日:2008-10-22
    标 题:Substituted pyrazolo[1,5-]pyrimidine compounds as intermediates in the synthesis of TRK kinase inhibitors

    专利号:ES-2588504-T3
    优先权日:2008-10-22
    标题 :Pyrazolo [1,5-a] pyrimidine compounds substituted as intermediates in the synthesis of TRK kinase inhibitors

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1021/acs.jmedchem.7b01351
    摘要:Krall J, Jensen CH, Bavo F, Falk-Petersen CB, Haugaard AS, Vogensen SB, Tian Y, Nittegaard-Nielsen M, Sigurdardóttir SB, Kehler J, Kongstad KT, Gloriam DE, Clausen RP, Harpsøe K, Wellendorph P, Frølund B. Molecular Hybridization of Potent and Selective γ-Hydroxybutyric Acid (GHB) Ligands: Design, Synthesis, Binding Studies, and Molecular Modeling of Novel 3-Hydroxycyclopent-1-enecarboxylic Acid (HOCPCA) and trans-γ-Hydroxycrotonic Acid (T-HCA) Analogs. J Med Chem. 2017 Nov 09;60(21):9022–39. doi: 10.1021/acs.jmedchem.7b01351.
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