CAS: 762287-59-2; 3-Fluoro-2-Methoxyphenylboronic Acid

该化合物是一种有机有机体化合物,其特点是,在以氟原子和甲氧组替代的苯环上有一个附着的碱酸性功能组,以氟原子和甲氧组为替代品,该化合物通常具有白色至非白色固体,极地有机溶剂中可溶性,在标准条件下具有中等稳定性等特性; 碱酸碱允许参与各种化学反应,特别是铃木联动反应,使其在有机合成和药用化学中具有价值; 氟素的存在可增强化合物的脂性和生物活动,而甲基氧组则可能影响其电子特性和再活动; 此外,已知的碱酸具有与二醇形成可逆复合体的能力,可在传感器应用和药物设计中加以利用.

结构式图片

欧盟法规

C&L通报

合成工艺路线路线简述

    在 盐酸体系中,化学反应生成 2-甲氧基-3-氟苯硼酸
    参考文献:Substituted 3-Amino Biaryl Propionic Acids As Potent Vla-4 Antagonists
    标题:Substituted 3-Amino Biaryl Propionic Acids As Potent Vla-4 Antagonists
    摘要:A Series Of Substituted N-(3,5-Dichlorobenzenesulfonyl)-(L)-Prolyl-And (L)-Azetidyl-Beta-Biaryl Beta-Alanine Derivatives Was Prepared As Selective And Potent Vla-4 Antagonists. The 2,6-Dioxygenated Biaryl Substitution Pattern Is Important For Optimizing Potency. Oral Bioavailability Was Variable And May Be A Result Of Binding To Circulating Plasma Proteins. (C) 2002 Elsevier Science Ltd. All Rights Reserved.
    DOI:10.1016/s0960-894X(02)00460-2

    海关参考信息

    专利信息


    专利号:CN-103384663-B
    优先权日:2010-12-23
    标题:Synthesis of intermediates for the preparation of anacetrapib and derivatives thereof

    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-9951062-B2
    优先权日:2012-12-14
    标 题 :Substituted 1 H-pyrrolo [2, 3-b] pyridine and 1 H-pyrazolo [3, 4-b] pyridine derivatives as salt inducible kinase 2 (SIK2) inhibitors
    发明人:VANKAYALAPATI HARIPRASAD; YERRAMREDDY VENKATAKRISHNAREDDY; GANIPISETTY VENU BABU; TALLURI SURESHKUMAR; APPALANENI RAJENDRA P
    权利人:ARRIEN PHARMACEUTICALS LLC
    摘要:Compounds according to Formulas I, IA or IB: n nto pharmaceutically acceptable composition, salts thereof, their synthesis and their use as SIK2 inhibitors including such compounds and methods of using said compounds in the treatment of various diseases and/or disorders such as cancer, stroke, cardiovascular, obesity and type II diabetes.

    专利号:US-9834551-B2
    优先权日:2013-04-18
    标 题 :Substituted pyrrolo[2,3-b]pyrazines and substituted pyrazolo[3,4-b]pyridines as ITK and JAK kinase inhibitors
    发明人:VANKAYALAPATI HARIPRASAD; YERRAMREDDY VENKATAKRISHNAREDDY; GANGIREDDY PARAMAREDDY; APPALANENI RAJENDRA P
    权利人:ARRIEN PHARMACEUTICALS LLC
    摘要:The present invention relates to compounds described by Formula I: n nsalts thereof, their synthesis, and their use as ITK and JAK3 inhibitors including such compounds and methods of using said compounds in the treatment of various diseases and or disorders such disease associated with abnormal cell growth such as autoimmune, inflammation, rheumatoid arthritis, systemic lupus erythematosus, atherosclerosis, ulcerative colitis, psoriatic arthritis, psoriasis, Crohn's, metabolic and cancer diseases. The present invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions and processes for preparing the compounds of the invention.
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