CAS: 304854-55-5; 3-Bromo-5-Chlorobenzonitrile

该化合物是一种卤代苯衍生物,广泛用作有机合成和制药研究的多用途中间体.其独特的替代模式,包括芳香环上的溴和氯组,能够有选择地发挥作用,使其对构建复杂的分子具有价值.该化合物的高度纯度和稳定性确保了交叉反应的可靠性能,如Suzuki 或 Buchwald-Hartwig 的结合以及核分裂生物替代反应.其硝酸组进一步加强了再活性,允许转化成碳箱酸,氨化物或其他功能组.该化合物在农业化学和药用化学中特别有助于开发生物活性分子.建议在不成熟的条件下进行适当的处理和储存以保持其完整性.

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2-氨基-3-溴-5-氯苯甲腈 2-Amino-3-Bromo-5-Chlorobenzonitrile 914636-84-3

合成工艺路线路线简述

    📜2-氨基-5-氯苯腈置于溴,亚硝酸异戊酯体系中,用 溶剂黄146,N,N-二甲基甲酰胺 用作溶剂,化学反应 0.17H,反应生成3-溴-5-氯苯腈
    参考文献:Potent Mglur5 Antagonists: Pyridyl And Thiazolyl-Ethynyl-3,5-Disubstituted-Phenyl Series
    标题:Potent Mglur5 Antagonists: Pyridyl And Thiazolyl-Ethynyl-3,5-Disubstituted-Phenyl Series
    摘要:We Report The Synthesis Of Four Series Of 3,5-Disubstituted-Phenyl Ligands Targeting The Metabotropic Glutamate Receptor Subtype 5: (2-Methylthiazol-4-yl)Ethynyl (1A-J,),(6-Methylpyridin-2-yl)Ethynyl (2A-J),(5-Methylpyridin-2-yl)Ethynyl (3A-J,),And (Pyridin-2-yl)Ethynyl (4A-J,). The Compounds Were Evaluated For Antagonism Of Glutamate-Mediated Mobilization Of Internal Calcium In An Mglur5 In Vitro Assay. All Compounds Were Found To Be Full Antagonists And Exhibited Low Nanomolar To Subnanomolar Activity. (C) 2011 Elsevier Ltd. All Rights Reserved.
    Doi:10.1016/j.Bmcl.2011.04.047

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1055/s-0037-1611517
    摘要:Synthesis of Ketones from Organolithium Reagents in Continuous Flow. Synfacts. 2019 Apr 15;2019(05):0577. doi: 10.1055/s-0037-1611517.
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