CAS: 5751-80-4; Ethyl Thiophene-3-Carboxylate

该化合物是一种有机化合物,其特点是用乙基碳箱状物组在3点对硫苯环进行酯化.该乙型环因其多功能性被视作合成有机化学的构件,特别是在制药,农用化学和功能材料的准备方面.其硫苯核心有助于产生富电子特性,增强交叉和循环反应的再活动.乙酯组提供了有利的溶性和加工特性,有利于进一步的衍生.该化合物的稳定性和定义明确的再活动特征使它成为构建复杂分子结构的可靠中间体.它通常用于需要硫苯基系统精确功能化的研究和工业应用中.

结构式图片

上下游产品

3-thiophene carboxylic acid chloride ethanol 3-Bromothiophene carbon monoxide5-ethyl-thiophene-3-carboxylic acid ethyl 2,5-diphenyl-3-thiophenecarboxylate ethyl 2,5-bis(4-methoxyphenyl)-3-thiophenecarboxylate 54H84O6S3Si3C54H84O6S3Si3

合成工艺路线路线简述

    3-噻吩甲酸置于硫酸体系中,用 乙醇 作为反应溶剂,以88%的收率获得产物噻吩-3-甲酸乙酯
    参考文献:苯并噻唑类化合物及医药用途
    标题:苯并噻唑类化合物及医药用途
    摘要:本发明公开了一种苯并噻唑类化合物及其医药用途,具体涉及如式i所示的苯并噻唑类化合物及其医药用途,尤其涉及苯并噻唑类化合物作为usp7C端结构域调控剂在预防和治疗骨髓增生异常综合征及恶性肿瘤的药物中的用途.本发明式i所示苯并噻唑类化合物或其药学上可接受的盐或溶剂化物与usp7C端蛋白具有很强的结合力,并可以降低肿瘤细胞中dnmt1的蛋白水平,因而可应用在制备usp7调控剂,同时具有显著的抗肿瘤细胞增殖作用,可以用于制备预防或治疗骨髓增生异常综合征及恶性肿瘤的药物.

    海关参考信息

    专利信息


    专利号:US-6051704-A
    优先权日:1996-07-22
    标题:Synthesis of macrocyclic tetraamido-N ligands
    发明人:GORDON-WYLIE SCOTT W; COLLINS TERRENCE J
    权利人:UNIV CARNEGIE MELLON
    摘要:New synthetic methods for the preparation of macrocyclic amido-N donor ligands are provided. The primary method of the present invention involves in general only two synthetic steps. In the first step, an α or β amino carboxylic acid is allowed to react with an optimal (approximately stoichiometric) amount of an activated malonate or oxalate derivative with mild heating. Upon completion of the double coupling reaction, hydrolysis of the reaction mixture yields a diamide containing intermediate (a macro linker). In the second step, stoichiometric amounts of a diamine, preferably an orthophenylene diamine, are added to the macro linker intermediate in the presence of a coupling agent and heat. This second double coupling reaction, is allowed to proceed for a period of time sufficient to produce a macrocyclic tetraamido compound. The substituent groups on the α or β amino carboxylic acid, the malonate, and the aryl diamine may all be selectively varied so that the resulting tetraamido macrocycle can be tailored to specific desired end uses. The macrocyclic tetraamide ligand may then be complexed with a metal, such as a transition metal, and preferably the middle and later transition metals, to form a robust chelate complex suitable for catalyzing oxidation reactions.

    专利号:US-7060818-B2
    优先权日:2003-02-21
    标题:Synthesis of macrocyclic tetraamido compounds and new metal insertion process
    发明人:HORWITZ COLIN P; GHOSH ANINDYA
    权利人:UNIV CARNEGIE MELLON
    摘要:An improved method of synthesizing a macrocyclic tetraamido compound includes protecting the amino portion of an amino carboxylic acid to form a protected amino carboxylic acid; exposing the protected amino carboxylic acid to a first solvent, preferably a hydrocarbon solvent, such as toluene or 1,2-dichloroethane, dichloromethane, dibromomethane and 1,2-dibromoethane. The carboxylic acid portion of the protected amino carboxylic acid is then converted to an activated carboxylic acid by one of esterification or acid halide formation, to form a protected amino activated carboxylic acid derivative. The protected amino activated carboxylic acid derivative is reacted with a diamine in the presence of a second solvent, such as THF or ,2-dichloroethane, dichloromethane, dibromomethane and 1,2-dibromoethane, to form a protected diamide diamine intermediate. Following deprotection, the diamide diamine intermediate is reacted with an activated diacid, such as an activated malonate, oxalate or succinate derivative to form the macrocyclic tetraamido compound. The macrocyclic tetraamido compound may further be complexed with a transition metal.

    专利号:US-9487539-B2
    优先权日:2009-09-18
    标 题 :Compounds and therapeutic use thereof for protein kinase inhibition
    发明人:WU ZHANGGUI
    权利人:WU ZHANGGUI
    摘要:Novel compound having the following formula: n nwherein Y is N, O, or S. Also disclosed are a pharmaceutical compositions comprising the same, methods for treating cancer using the same, and methods for the synthesis of the same. The novel compounds of the present invention are found to inhibit protein kinases, especially Checkpoint kinase Chk1/Chk2.

    专利号:WO-2018170851-A1
    优先权日:2017-03-23
    标题 :Imide-containing ladder tpye heteroarenes: synthesis and ralated organic semiconductor devices
    发明人:GUO XUGANG; WANG YINGFENG; GUO HAN; LING SHAOHUA
    权利人:UNIV SOUTH SCIENCE & TECHNOLOGY CHINA
    摘要:Small molecule and polymer semiconductors and their preparation methods are provided. These compounds are of formula I-III, and can be used in high-mobility organic thin-film transistors and bulk heterojunction polymer solar cells.

    专利号:US-2004167329-A1
    优先权日:2003-02-21
    标 题:Synthesis of macrocyclic tetraamido compounds and new metal insertion process

    专利号:CN-106749318-A
    优先权日:2016-11-22
    标题:A kind of organic field effect transistor material based on oxygen heterofused rings and its synthesis method and application
    南京新斯特生物科技有限公司
    ⚠️ 未注册 · 未认证企业
    ⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
    数据来源于公开网络搜索,平台未作核实,请自行辨别。
    🏢敬请 企业认领
    🏬开设公司展台
    📢获取免费会员权益
    🎖️点亮专属注册企业标签
    📇展现公司完整信息 样本查看立即注册认领 →
    网址: http://www.nstbio.com
    企业联系电话:025-85331029,18915981017👤
    📞南京新斯特生物科技有限公司 ⚠️参考联系方式
    联系人:杨女士
    电话:025-85331029,18915981017
    手机:18915981017
    传真:025-85331829
    邮箱:sales@nstbio.com
    通信地址: 江苏省南京市栖霞区纬地路9号江苏省生命科技创新园F6栋10楼
    邮编: 210010
    🆔 联系时候可告知是从"百琢研"平台获取的信息.
    ⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

    地址:江苏省南京市栖霞区纬地路9号江苏省生命科技创新园F6栋10楼
    ⚠️ 未注册 · 未认证企业
    注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
    ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
    第 1 / 1 页
    现货

    供应商参考报价(招募中)

    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


    摘要:Schatz, J.; Seler, M., Science of Synthesis Knowledge Updates, (2011) 2, 388.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知