CAS: 124959-28-0; 2-Chloro-4-(Furan-2-yl)Pyrimidine

该化合物是一种杂交有机化合物,其特点是存在一个以氯原子和皮质基组替代的火水晶环,分子结构中含有一个含有1号站点和3号站位两个氮原子的六人环和2号站站位氯原子的五人环,该产品是一座含有二氧化原子的七人环.该产品来自呋喃,其产自pyrimidine环的第4号站位置,它有助于化合物的独特特性.该化合物一般在室内温度下是固体,在有机溶剂中表现出中等溶解性.该物质具有潜在的生物活动,包括抗微生物和抗草药特性,因此对医药化学和农业应用很感兴趣.氯和呋喃亚体的存在可以影响化合物的再活动及其与生物目标的相互作用.在处理和使用时,应当参考安全数据,因为卤化合物可能对环境和健康造成风险.

结构式图片

相似化合物

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上下游产品

CAS号3934-20-1 2,4-二氯嘧啶 | CAS号118486-94-5 2-(三丁基锡烷基)呋喃 | CAS号110-00-9 呋喃 | CAS号1722-12-9 2-氯嘧啶

合成工艺路线路线简述

    📜2-Chloro-4-(Furan-2-yl)-1,4-Dihydropyrimidine置于2,3-二氯-5,6-二氰基-1,4-苯醌体系中,用 四氢呋喃,水 用作溶剂,化学反应 0.25H,反应生成2-氯-4-(2-呋喃基)嘧啶
    参考文献:Strekowski,Lucjan; Harden,Donald B.; Grubb,William B.,Journal Of Heterocyclic Chemistry,1990,Vol. 27,# 5,P. 1393-1400
    标题:Strekowski,Lucjan; Harden,Donald B.; Grubb,William B.,Journal Of Heterocyclic Chemistry,1990,Vol. 27,# 5,P. 1393-1400

    专利信息


    专利号:US-4021457-A
    优先权日:1975-11-18
    标 题 :Intermediates for polycyclic quinonoid antibiotics
    发明人:KENDE ANDREW S; MILLS JOHN E; TSAY YUH-GENG
    权利人:RESEARCH CORP
    摘要:There is provided a novel method of synthesizing certain tetracyclic quinones. In particular, there is provided a novel route to the synthesis of certain analogs of (+)-7-deoxydaunomycinone which includes the provision of novel tri- and tetracyclic quinone intermediates. The products of the synthetic route provided herein may be converted into compounds of known anti-neoplastic activity.

    专利号:US-4147706-A
    优先权日:1975-11-18
    标 题 :Intermediates for polycyclic quinonoid antibiotics
    发明人:KENDE ANDREW S; MILLS JOHN E; TSAY YUH-GENG
    权利人:RESEARCH CORP
    摘要:There is provided a novel method of synthesizing certain tetracyclic quinones. In particular, there is provided a novel route to the synthesis of (+)-7-deoxydaunomycinone and analogs thereof, which includes the provision of novel tri- and tetracyclic quinone intermediates. The -7-deoxydaunomycinone derived from naturally occurring daunomycin is a known compound, which is itself an intermediate in the preparation of the clinically accepted anti-tumor antibiotics daunomycine and its derivative adriamycin.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1055/s-0028-1087347
    摘要:Mongin F, Seggio A, Jutand A, Priem G. Synthesis of Unsymmetrical Heterobiaryls Using Palladium-Catalyzed Cross-Coupling Reactions of Lithium Organozincates. Synlett. 2008 Nov 12;2008(19):2955–60. doi: 10.1055/s-0028-1087347.
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