CAS: 186498-02-2; (4-Morpholinophenyl)Boronic Acid

该化合物是一种含有单硫代苯环的boronic酸衍生物,它成为有机合成和交叉组合反应特别是铃木-米亚乌拉相联反应的宝贵中间体,其电子富含的morphone mothine modioity在催化变异变中增强了反应性和选择性,便利了复杂的双子宫结构的建造.该化合物在标准处理条件下表现出了良好的稳定性,在普通有机溶剂中可溶解,确保了合成应用的易用性.其定义明确的结构和一贯的纯度使其适合于药物研究,材料科学和催化剂的开发.该产品典型的特点是NMR和HPLC,以确保高质量和高可再生于要求的合成工作流程.

结构式图片

欧盟法规

C&L通报

上下游产品

4-bromophenyl-morpholine 1,4-bromoiodobenzene 1-acetyl-7-[4-(N-morpholino)phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylic acid 4'-morpholin-4-yl-4-trifluoromethoxy-biphenyl-3-carboxylic acid [2-cyano-1-(1H-indol-3-ylmethyl)-ethyl]-amide N-(4-(2-methylpyridin-4-yl)phenyl)-2-(6-(4-morpholinophenyl)pyridin-2-yl)propanamide

合成工艺路线路线简述

    4-(4-溴苯基)吗啉置于正丁基锂,硼酸三异丙酯体系中,用 四氢呋喃,乙酸乙酯,正戊烷 用作溶剂,化学反应生成4-吗啉苯硼酸
    参考文献:Rho-Kinase Inhibitors
    标题:Rho-Kinase Inhibitors
    摘要:公开了化合物及其衍生物,它们的合成,以及它们作为rho激酶抑制剂的应用.本发明的这些化合物可用于抑制肿瘤生长,治疗勃起功能障碍,以及治疗其他由rho激酶介导的疾病,例如冠心病.

    海关参考信息

    专利信息


    专利号:US-11767302-B2
    优先权日:2020-10-01
    标题 :Reagents and methods for tetrazine synthesis
    发明人:FOX JOSEPH M; LAMBERT WILLIAM; FANG YINZHI; AM ENDE CHRISTOPHER WILLIAM; MAHAPATRA SUBHAM; XIE YIXIN; WANG CHUANQI
    权利人:UNIV DELAWARE
    摘要:Disclosed herein are mono- and di-substituted tetrazines and methods of their preparation and converting an oxetanyl ester to a thio-substituted tetrazine, which is then converted to a mono-substituted tetrazine, a di-substituted tetrazine, or a vinylether disubstituted tetrazine.

    专利号:US-7585875-B2
    优先权日:2006-06-06
    标 题 :Substituted pyrazolo[1,5-a]pyridine compounds and their methods of use
    发明人:GAETA FEDERICO C A; GROSS MATTHEW; JOHNSON KIRK W
    权利人:AVIGEN INC
    摘要:The present invention is directed to substituted pyrazolo[1,5-a]pyridines and related methods for their synthesis and use.

    专利号:US-2025026766-A1
    优先权日:2022-01-12
    标题 :Thiazolopyridyl Amide Derivatives as DNA Polymerase Theta Inhibitors
    发明人:LI JING; XU WENQING; WANG ZHIWEI
    权利人:BEIGENE LTD
    摘要:The present invention relates to compounds containing thiazolopyridyl amide structure, the process for their synthesis, as well as the use of such compounds for inhibiting DNA Polymerase Theta (Pol Theta), and in the treatment of various diseases including cancers.

    专利号:US-7648986-B2
    优先权日:2002-01-10
    标题:Substituted thieno[3,2-D]pyrimidines as Rho kinase inhibitors
    发明人:NAGARATHNAM DHANAPALAN; KHIRE UDAY; ASGARI DAVOUD; SHAO JIANXING; LIU XIAO-GAO; WANG CHUNGUANG; HART BARRY; WEBER OLAF; LYNCH MARK; ZHANG LEI; WANG LEI
    权利人:BAYER HEALTHCARE LLC
    摘要:Disclosed are compounds and derivatives thereof their synthesis, and their use as Rho-kinase inhibitors. These compounds of the present invention are useful for inhibiting tumor growth, treating erectile dysfunction, and treating other indications mediated by Rho-kinase, e.g., coronary heart disease.
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    合成参考文献


    摘要:Kashemirov, B. A.; Błażewska, K.; Justyna, K.; Lyu, J.; McKenna, C. E., Science of Synthesis Knowledge Updates, (2021) 1, 411.
    摘要:Migliorini, F.; Puglioli, S.; Neri, D.; Cazzamalli, S.; Favalli, N., Science of Synthesis: DNA-Encoded Libraries, (2024) nan, 108.
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