CAS: 38696-21-8; 5-Bromo-N,N-Dimethylpyrimidin-2-Amine

该化合物是一种化学化合物,其特点是其火利米丁环结构,这是一个由六人组成的芳香环,在1号位置和3号位置上含有两个氮原子. 在5号位置上存在一个溴原子,有助于其再活性和在各种化学反应中的潜在应用.2号位置的二甲基氨基组增强了其在极地溶剂中的基本性和溶解性.该化合物通常用于有机合成,并可作为生产药物或农用化学品的一个中间体.其分子结构允许各种功能化反应,使其成为医药化学中具有多种功能的建筑块.此外,该化合物的特性,如熔点,沸点和溶解性,可以因环境条件和其他物质的存在而有所不同.在处理和储存时,应参考安全数据,因为卤化化合物可能具有特定危害.

结构式图片

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31402-54-7 433684-23-2 77476-95-0

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CAS号7752-82-1 2-氨基-5-溴嘧啶 | CAS号74-88-4 碘甲烷 | CAS号53939-30-3 5-溴-2-氯吡啶 | CAS号124-40-3 二甲胺 | CAS号5621-02-3 2-二甲氨基嘧啶 | CAS号506-59-2 盐酸二甲胺 | CAS号32779-36-5 5-溴-2-氯嘧啶 | CAS号1072-97-5 2-氨基-5-溴吡啶 | CAS号1032759-30-0 2-二甲基胺嘧啶-5-硼酸-2... | CAS号55338-76-6 2-(二甲氨基)嘧啶-5-腈 | CAS号56621-99-9 N2,N2-二甲基-2,5-二氨基吡啶

合成工艺路线路线简述

    2-二甲氨基嘧啶置于1,3-二溴-5,5-二甲基海因体系中,用 二氯甲烷 作为反应溶剂,以86%的收率获得产物5-溴-2-(二甲基氨基)嘧啶
    参考文献:Syntheses And Properties Of Novel Liquid Crystals Containing A Trifluoromethylamino Group
    标题:Syntheses And Properties Of Novel Liquid Crystals Containing A Trifluoromethylamino Group
    摘要:含三氟甲基氨基团的液晶(lcs)是通过 P-溴取代的(杂)芳基(三氟甲基)胺与相应的二硫氨基甲酸酯经过氧化脱硫-氟化反应的交叉偶联反应制备的.新型液晶在较宽的温度范围内主要表现出层状相.它们作为向列相液晶的组成部分,其电光性能与相应的甲基胺进行了比较.
    DOI:10.1246/bcsj.72.2523

    海关参考信息

    专利信息


    专利号:US-5304647-A
    优先权日:1988-02-09
    标题:Method of preparation of halogenated diazines
    发明人:STREKOWSKI LUCJAN; MOKROSZ MARIA; HARDEN DONALD B
    权利人:UNIV GEORGIA STATE
    摘要:A method of preparation of substituted halogenodiazines which are useful as intermediates in the synthesis of novel unfused heterobicyclic compounds, and the products thereof. The reaction consists of the addition of an organolithium reagent with subsequent dehydrogenation of the addition product. The reaction takes place in one reaction vessel, without isolation of the substituted halogenodihydrodiazine intermediate. The reactions proceed at moderate temperature and in a short amount of time, which decreases the probability of side reactions and increases yield. Furthermore, the workup step is conducted under two-phase conditions to prevent hydrolysis of the substituted halogenodiazine to a substituted hydroxydiazine. The method is easy, efficient and results in a high yield of product. The substituted halogenodiazines are used as intermediates in the synthesis of unfused heterobicyclic compounds containing an aromatic moiety, diazine, and another aromatic moiety, such as thiophene, benzene, or naphthalene, which have biological activity.

    专利号:US-4963676-A
    优先权日:1988-02-09
    标题 :Di-substituted phthalazines
    发明人:STREKOWSKI LUCJAN; MOKROSZ MARIA; HARDEN DONALD B
    权利人:UNIV GEORGIA STATE
    摘要:A method of preparation of substituted halogenodiazines which are useful as intermediates in the synthesis of novel unfused heterobicyclic compounds, and the products thereof. The reaction consists of the addition of an organolithium reagent with subsequent dehydrogenation of the addition product. The reaction takes place in one reaction vessel, without isolation of the substituted halogenodihydrodiazine intermediate. The reactions proceed at moderate temperature and in a short amount of time, which decreases the probability of side reactions and increases yield. Furthermore, the workup step is conducted under two-phase conditions to prevent hydrolysis of the substituted halogenodiazine to a substituted hydroxydiazine. The method is easy, efficient and results in a high yield of product. The substituted halogenodiazines are used as intermediates in the synthesis of novel unfused heterobicyclic compounds containing an aromatic moiety, diazine, and another aromatic moiety, such as thiophene, benzene, or naphthalene, which have biological activity.
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    合成参考文献


    摘要:von Angerer, S., Science of Synthesis Knowledge Updates, (2011) 1, 408.
    摘要:Liu, S.; Xiao, J., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 233.
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