CAS: 1194-78-1; 6-Chloropyrimidine-2,4,5-Triamine

该化合物是一种具有三氨基替代模式的氯化火利米丁衍生物,为异环合成提供了多种功能,其结构是制备药品,农用化学品和特殊化学品的关键中间体.多种氨基化合物的存在增强了其核分裂性,使选择性功能化成为可能,而氯替代成分则为进一步衍生提供了一个反应场所.该化合物在药用化学中特别有用,用于建造有引信的火利米丁系统或作为代谢物的前体.在标准条件下稳定,与普通有机溶剂的兼容性有助于多步骤合成途径的处理.平衡性反作用特征使其成为定制分子结构的一个实用建筑块.

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4316-98-7 130838-36-7 156-83-2

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2,5-diamino-4,6-dichloropyrimidine -2,4-pyrimidinediamine6-chloro-5-(4-chlorophenyl)azo-2,4-pyrimidinediamine ethyl 2-cyanoacetate 7-chloro-1H-[1,2,3]triazolo[4,5-d]pyrimidine-5-amine 2-amino-6-chloropurine

合成工艺路线路线简述

    📜2,5-二氨基-4,6-二氯嘧啶置于ammonium Hydroxide体系中,化学反应 24.0H,以93%的收率获得2,4,5-三氨基-6-氯嘧啶
    参考文献: Compounds For Treating Cystic Fibrosis[fr] Composés Pour Le Traitement De La Fibrose Kystique
    标题: Compounds For Treating Cystic Fibrosis[fr] Composés Pour Le Traitement De La Fibrose Kystique

    专利信息


    专利号:US-10676445-B1
    优先权日:2019-06-06
    标 题:Synthesis of aminopyrimidine-based energetic materials
    发明人:WILHELM CHRISTOPHER; FOROHAR FARHAD; SOTO DENISSE
    权利人:US NAVY
    摘要:A new azido compound, 5-amino-6-chloro-2,4-diazido-pyrimidine, and a process for synthesizing. The synthesis may include reacting 5-amino-2,4,6-trichloropyrimidine and sodium azide. There is an excess molar amount of sodium azide for each chloro fractional molar amount on the 5-amino-2,4,6-trichloropyrimidine. The synthesis is a two phase reaction that is a dispersion. The 5-amino-2,4,6-trichloropyrimidine dissolved in acetone is a liquid phase, and the sodium azide is insoluble in acetone and is a solid phase, that is present in excess of chemical equivalents. The reaction product is soluble in acetone, and the reaction by-product, sodium chloride is also insoluble in acetone, and the crude yield is about 92%. Unreacted sodium azide and formed sodium chloride are removed by filtration.

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1016/s0166-3542(99)00019-4
    摘要:Hisaki M, Imabori H, Azuma M, Suzutani T, Iwakura F, Ohta Y, Kawanishi K, Ichigobara Y, Node M, Nishide K, Yoshida I, Ogasawara M. Synthesis and anti-influenza virus activity of novel pyrimidine derivatives. Antiviral Res. 1999 Jun;42(2):121–37. doi: 10.1016/s0166-3542(99)00019-4.
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