CAS: 859166-87-3; (4-Fluoropyridin-2-yl)Methanamine

该化合物是一种氟虫胺衍生物,在环的2位置上具有氨基甲基替代成分,该化合物是制药和农用化学合成的多用途建筑块,氟原子可增强代谢稳定性和生物利用率.主要含汞功能允许进一步衍生,使氨化物,非丁胺或其他含氮的乙型循环体得以形成.其硬性丙烯核心有助于改进目标相互作用的结合性,使其在药物发现药物的药用化学中具有价值.电排氟化合物的替代成分还影响再活性,便利选择性的改变.由于潜在的敏感性,在惰性条件下使用是合适的.

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上下游产品

4-氟吡啶-2-甲腈 4-Fluoropyridine-2-Carbonitrile 847225-56-3

合成工艺路线路线简述

    📜3-(2-Fluoro-Pyridin-4-yl)-Benzaldehyde置于吡啶,乙酸酐,水,Tin(Ll) Chloride体系中,用 二氯甲烷,Dmf (N,N-Dimethyl-Formamide) 作为反应溶剂,化学反应 26.0H,反应生成 2-氨甲基-4-氟吡啶
    参考文献: Ornithine Derivatives As Prostaglandin E2 Agonists Or Antagonists[fr] Derives D'Ornithine Utilises Comme Agonistes Ou Antagonistes De La Prostaglandine E2
    标题: Ornithine Derivatives As Prostaglandin E2 Agonists Or Antagonists[fr] Derives D'Ornithine Utilises Comme Agonistes Ou Antagonistes De La Prostaglandine E2

    海关参考信息

    专利信息


    专利号:EP-1875239-B1
    优先权日:2005-04-27
    标题 :A method for the preparation of imaging probes using click chemistry
    发明人:KOLB HARTMUTH C; MOCHARLA VANI P; WALSH JOSEPH C
    权利人:SIEMENS MEDICAL SOLUTIONS
    摘要:The invention provides a method for identifying a candidate imaging probe, the method comprising: a) contacting a first library of candidate compounds with a target biomacromolecule, b) identifying a first member from the first library exhibiting affinity for the first binding site; c) contacting the first member identified from the first library affinity for the first binding site with the target biomacromolecule; d) contacting a second library of candidate compounds with the first member and the target biomacromolecule, e) reacting the complementary first functional group with the second functional group via a biomacromolecule induced click chemistry reaction to form the candidate imaging probe; f) isolating and identifying the candidate imaging probe; g) preparing the candidate imaging probe by chemical synthesis; and h) for imaging applications, converting the candidate imaging probe into an imaging probe.

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