CAS: 1848-84-6; 2-Ethyl-1H-Benzo[d]Imidazole

该化合物是一种有机化合物,其特征为引信环结构,由苯环和imidazole环组成,是苯并氨酸的衍生物,在苯苯环的第二个位置替换乙基组,该化合物一般是白色的,是非白色固体的,在有机溶剂中可溶解,由于存在imidazole氮,具有基本特性,因此有可能成为协调化学的一个离子体. 2-乙基苯并氨因其在包括制药在内的各个领域的应用而闻名,可以作为生物活性化合物合成的中间体.此外,该化合物在加强某些金属复合体稳定性方面的潜在作用已经进行了研究.该化合物的再活性可能受到功能组的存在和分子的整体电子环境的影响,因此它成为有机合成和药用化学的一个主题.应当参考安全数据,以便处理和接触任何化学物质时使用.

结构式图片

相似化合物

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合成工艺路线路线简述

    2-Cyano-1,3-Bis(Ethoxycarbonyl)-2,3-Dihydrobenzimidazole置于苯甲酸,Lithium Diisopropyl Amide体系中,用 四氢呋喃,正己烷 用作溶剂,化学反应 29.0H,反应生成2-乙基苯并咪唑
    参考文献:Uff,Barrie C.; Ho,Yee-Ping; Burford,Donald L. W.,Journal Of Heterocyclic Chemistry,1987,Vol. 24,P. 1349-1351
    标题:Uff,Barrie C.; Ho,Yee-Ping; Burford,Donald L. W.,Journal Of Heterocyclic Chemistry,1987,Vol. 24,P. 1349-1351

    海关参考信息

    专利信息


    专利号:US-2012328569-A1
    优先权日:2010-03-02
    标题:Inhibitors of hepatitis c virus ns5b polymerase
    发明人:MCCOMAS CASEY CAMERON; LIVERTON NIGEL J; SOLL RICHARD; LI PENG; PENG XUANJIA; WU HAO; NARJES FRANK; HABERMANN JOERG; KOCH UWE; LIU SHILAN
    权利人:MCCOMAS CASEY CAMERON; LIVERTON NIGEL J; SOLL RICHARD; LI PENG; PENG XUANJIA; WU HAO; NARJES FRANK; HABERMANN JOERG; KOCH UWE; LIU SHILAN
    摘要:Disclosed are compounds of formula (I) that are used as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

    专利号:US-11708320-B2
    优先权日:2018-06-29
    标 题:Environmentally-friendly hydroazidation of olefins
    发明人:XU HAO
    权利人:UNIV GEORGIA STATE RES FOUND
    摘要:The present invention provides processes for the synthesis of organic azides, intermediates for the production thereof, and compositions related thereto.

    专利号:US-2005249675-A1
    优先权日:2003-06-19
    标 题 :Mucin synthesis inhibitors
    发明人:HUNG HSIAO-LING; CHELLQUIST ERIC; LEVITT ROY C; MCLANE MICHAEL
    权利人:HUNG HSIAO-LING; CHELLQUIST ERIC; LEVITT ROY C; MCLANE MICHAEL
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases.

    专利号:US-7345051-B2
    优先权日:2000-01-31
    标题 :Mucin synthesis inhibitors
    发明人:ZHOU YUHONG; LEVITT ROY C; NICOLAIDES NICHOLAS C; JONES STEVE; MCLANE MIKE
    权利人:GENAERA CORP
    摘要:The claimed invention relates to methods of modulating mucin synthesis and the therapeutic application of compounds of Formula II in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (COPD) including asthma and chronic bronchitis, inflammatory lung diseases, cystic fibrosis and acute or chronic respiratory infectious diseases. n nwhereinn X is S, N, O or CR; Y is CRR′, O, NR 6 , CRR′—CRR′ or CRâ•?CR; Z is NR 6 , O, S, CRR′ or CRR′—CRR′; R 1 -R 3 are independently selected from the group consisting of H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, amino, hydroxy, halosubstituted alky and halo; R 4 is n n n n n n n n n n n n n n n n n n n Q is CR, NR 6 or n n n n n n n n n n n n R 5 is H or benzyl; n R 6 is H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, OH or halo; and n R and R′ are independently H, C 1 -C 8 alkyl, C 1 -C 8 alkoxy, OH or halo,n nor a harmaceutically acceptable salt thereof.

    专利号:US-8772301-B2
    优先权日:2009-12-18
    标题 :Compounds for treating disorders mediated by metabotropic glutamate receptor 5, and methods of use thereof
    发明人:HARDY LARRY WENDELL; HEFFERNAN MICHELE L R; WU FRANK XINHE; SPEAR KERRY L; SARASWAT LAKSHMI D
    权利人:HARDY LARRY WENDELL; HEFFERNAN MICHELE L R; WU FRANK XINHE; SPEAR KERRY L; SARASWAT LAKSHMI D; SUNOVION PHARMACEUTICALS INC
    摘要:Provided herein are compounds and methods of synthesis thereof. The compounds set forth herein are useful for the treatment, prevention, and/or management of various disorders, such as neurological disorders, neurodegenerative disorders, neuropsychiatric disorders, disorders of cognition, learning or memory, gastrointestinal disorders, lower urinary tract disorder, and cancer. Compounds set forth herein modulate the activity of metabotropic glutamate receptor 5 (mGluR5) in the central nervous system or the periphery. Pharmaceutical formulations containing the compounds and their methods of use are also provided herein.

    专利号:US-10995078-B2
    优先权日:2013-03-13
    标 题:Compounds and compositions for inhibition of FASN
    发明人:BAIR KENNETH W; LANCIA JR DAVID R; LI HONGBIN; LOCH JAMES; LU WEI; MARTIN MATTHEW W; MILLAN DAVID S; SCHILLER SHAWN E R; TEBBE MARK J
    权利人:FORMA THERAPEUTICS INC
    摘要:The present invention relates to compounds and composition for inhibition of FASN, their synthesis, applications, and antidotes. An illustrative compound of the invention is shown below:
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    合成参考文献


    参考文献:10.1107/s1600536811010774
    摘要:Li SJ, Liu JH, Song WD, Li XF, Miao DL. 2-Ethyl-1H-imidazole-4-carboxyl-ate monohydrate. Acta Crystallogr Sect E Struct Rep Online. 2011 Apr 01;67(Pt 4):o996–7.
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