CAS: 737000-76-9; (3,5-Difluoro-2-Methoxyphenyl)Boronic Acid

该化合物是一种有机有机体化合物,其特征是配在替代芳香环上的碳酸功能组;分子结构在苯环的3和5个位置上有两个氟原子,可影响其电子特性和再活性;2位置的甲基氧组可增强各种溶剂中化合物的溶性性和稳定性;该化合物通常用于有机合成,特别是用于相互交错的反应,如铃木-米亚拉交配,这对形成碳-碳结层很有价值;该碳酸组的存在有助于形成含有二醇的稳定复合体,从而在包括药用化学和材料科学在内的各种应用中有用;此外,氟基亚组可产生独特的特性,如增加脂性并改变生物活动;

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上下游产品

CAS号202865-59-6 2-溴-4,6-二氟苯甲醚 | CAS号1150114-51-4 3,5-二氟-2-羟基苯硼酸

合成工艺路线路线简述

  • 合成目标产物 (3,5-Difluoro-2-Methoxyphenyl)Boronic Acid, 97 主要起始原料 2-Bromo-4,6-Difluoroanisole
  • (文献来源)合成步骤主要原料 2-Bromo-4,6-Difluoroanisole
📜2-溴-4,6-二氟苯甲醚置于正丁基锂,硼酸三异丙酯,盐酸体系中,用 四氢呋喃,乙醚 作为反应溶剂,化学反应 0.53H,以228 Mg的收率获得产物3,5-二氟-2-甲氧基苯硼酸
参考文献:Synthetic Chemistry-Led Creation Of A Difluorinated Biaryl Ether Non-Nucleoside Reverse Transcriptase Inhibitor
标题:Synthetic Chemistry-Led Creation Of A Difluorinated Biaryl Ether Non-Nucleoside Reverse Transcriptase Inhibitor
摘要:在新开发的一系列含氟联苯醚结构的非核苷逆转录酶抑制剂中,我们偶然发现了衍生物20,它对野生型及临床相关突变型的逆转录酶均表现出卓越的抑制效力.
DOI:10.1039/b714091F

海关参考信息

专利信息


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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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献

参考DOI号:10.1039/b714091f
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