CAS: 54143-56-5; N-(Piperidin-2-Ylmethyl)-2,5-Bis(2,2,2-Trifluoroethoxy)Benzamide Acetate

该化合物是一种主要用作治疗某些类型心血管不全的抗亚胺剂的药物化合物,它属于钠渠道阻塞器类别,在心脏行动潜力的脱冰阶段抑制钠离子流入,从而稳定心膜,降低易感性能.该物质通常以其乙酸盐形式施用,这增加了其溶解性和生物利用率.氟化碳乙酸乙酸酯的特点是其相对高的亲利性,使其能够有效渗透细胞膜.它具有中度半衰期,需要谨慎地努力保持治疗水平.常见副作用包括惊呆,视觉干扰和潜在的心血管效应,特别是在有结构性心脏病的病人中.由于它的威力,它通常被谨慎地处方,并建议在治疗期间定期监测心脏功能.

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CAS号57415-36-8 N-(2-吡啶基甲基)-2,5... | CAS号64-19-7 冰醋酸 | CAS号54143-55-4 氟卡尼

合成工艺路线路线简述

    📜N-(2-吡啶基甲基)-2,5-二(2,2,2-三氟乙氧基)苯甲酰胺置于pt-C体系中,用 溶剂黄146 作为反应溶剂,以89%的收率获得产物醋酸氟卡尼
    参考文献:&agr;,&agr;-Dibromo-&agr;-Chloro-Acetophenones As Synthons
    标题:&agr;,&agr;-Dibromo-&agr;-Chloro-Acetophenones As Synthons
    摘要:这项披露涉及使用α,α-二溴-α-氯乙酰苯酮化合物作为制备芳香酮化合物的中间体,特别是芳香酰胺.化合物2,5-双(2,2,2-三氟乙氧基)-α,α-二溴-α-氯乙酰苯酮尤其适用于制备已知药物非卡因.

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    专利信息


    专利号:US-10925977-B2
    优先权日:2006-10-05
    标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications
    发明人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S
    权利人:YANG DAVID J; YU DONGFANG; THOMPSON ANDREW S; CEIL POINT LLC; UNIV TEXAS
    摘要:Novel methods of synthesis of chelator-targeting ligand conjugates, compositions comprising such conjugates, and therapeutic and diagnostic applications of such conjugates are disclosed. The compositions include chelator-targeting ligand conjugates optionally chelated to one or more metal ions. Methods of synthesizing these compositions in high purity are also presented. Also disclosed are methods of imaging, treating and diagnosing disease in a subject using these novel compositions, such as methods of imaging a tumor within a subject and methods of diagnosing myocardial ischemia.

    专利号:US-7196197-B2
    优先权日:2003-09-17
    标题:Process for the preparation of Flecainide, its pharmaceutically acceptable salts and important intermediates thereof
    发明人:WANG ZHI-XIAN; LI YUANQIANG; GUNTOORI BHASKAR REDDY
    权利人:APOTEX PHARMACHEM INC
    摘要:Process for the preparation of Flecainide, its pharmaceutically acceptable salts and important intermediates thereof that involves the use of the 2-halobenzoic acid and its derivatives as a starting material. The use of this process also allows for the synthesis of a novel intermediate useful in the production of Flecainide. This new process is an inexpensive and efficient process for the manufacture of these compounds.

    专利号:US-6599922-B2
    优先权日:2001-08-10
    标 题:Process for the preparation of 2,5-bis-(2,2,2-trifluoroethoxy)-N-(2-piperidylmethyl)-benzamide (FLECAINIDE)
    发明人:VIGANO ENRICO; PIZZATTI ENRICA; MOLTENI RENATO; LANFRANCONI SIMONA
    权利人:A M S A ANONIMA MATERIE SINT E
    摘要:Process for the synthesis of FLECAINIDE comprising the reaction between 2,5-dihydroxybenzoic acid with trifluoroethanol perfluorobutanesulphonate to give the intermediate trifluoroethanol 2,5-bis-trifluoroethoxybenzoate, the reaction of said intermediate with 2-aminomethylpiperidine to give FLECAINIDE.

    专利号:US-7825268-B2
    优先权日:2003-12-23
    标 题:Alkoxylactones, alkoxylactams and alkoxythiolactams for controlling processes based on microbial interaction
    发明人:STUMPE STEFAN; BREVES ROLAND; HUCHEL URSULA; JANSSEN FRANK; HAETZELT ANDRE
    权利人:HENKEL AG & CO KGAA
    摘要:Compounds of the Formula I, n nwherein A 1 is O or NH; A 2 is O or S; each of R 1 and R 2 is independently hydrogen, a methyl or C 2 -C 8 -saturated or mono- or doubly unsaturated, branched or linear hydrocarbon group; and R 3 is a C 1 -C 18 -saturated or mono- or doubly unsaturated, branched or linear hydrocarbon group wherein, each of R 1 , R 2 and R 3 comprises a heteroatom selected from the group consisting of O and S in the chain and/or is mono- or multiply-substituted by a substituent selected from the group consisting of halogen, hydroxy, C 1 -C 6 -alkyl, trifluoromethyl, C 1 -C 6 -alkoxy, C 6 -C 10 -aryl, and C 1 -C 6 -alkyl-C 6 -C 10 -aryl are useful for controlling the interaction process between microorganisms such as in the development and/or maturation of biofilms; multicellular swarm behavior; the concerted development of antibiotic resistances; the concerted synthesis of antibiotics; the concerted synthesis of pigments; the concerted production of extracellular enzymes; or the concerted production of virulence factors.

    专利号:US-10814013-B2
    优先权日:2006-10-05
    标 题 :Efficient synthesis of chelators for nuclear imaging and radiotherapy: compositions and applications

    专利号:US-2008107598-A1
    优先权日:2006-10-05
    标 题:Efficient Synthesis of Chelators for Nuclear Imaging and Radiotherapy: Compositions and Applications

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Benoit A, Paolucci M, Stefan L, Vanderperren O, Hoffer E. [A CASE OF FLECAINIDE INTOXICATION]. Rev Med Liege. 2015 Sep;70(9):442-5. Review. French. doi: 10.1007/s00228-015-1832-0. Epub 2015 Apr 15. Review.
    3: Andrikopoulos GK, Pastromas S, Tzeis S. Flecainide: Current status and perspectives in arrhythmia management. World J Cardiol. 2015 Feb 26;7(2):76-85. doi: 10.4330/wjc.v7.i2.76. Review.
    4: Apostolakis S, Oeff M, Tebbe U, Fabritz L, Breithardt G, Kirchhof P. Flecainide acetate for the treatment of atrial and ventricular arrhythmias. Expert Opin Pharmacother. 2013 Feb;14(3):347-57. doi: 10.1517/14656566.2013.759212. Epub 2013 Jan 7. Review. doi: 10.1016/j.tcm.2012.06.008. Epub 2012 Aug 4. Review. doi: 10.2165/11599950-000000000-00000. Review. doi: 10.1093/europace/euq517. Epub 2011 Feb 2. Review. doi: 10.1093/europace/euq382. Epub 2010 Dec 7. Review.

    合成参考文献


    摘要:Iyakuhin Kenkyu. Study of Medical Supplies., 22(967), 1991
    摘要:American Journal of Cardiology., 53(329), 1984 []
    摘要:Gekkan Yakuji. Pharmaceuticals Monthly., 41(1714), 1999
    摘要:American Journal of Cardiology., 55(1643), 1985 []
    摘要:Connectical Medicine., 54(183), 1990
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