CAS: 69004-04-2; 1-Methyl-3-(3-Methyl-4-(4-((Trifluoromethyl)Sulfonyl)Phenoxy)Phenyl)-1,3,5-Triazinane-2,4,6-Trione

该化合物是一种化学化合物,主要被确认为用于抗寄生物剂,特别是兽用药;它是三联苯化合物类别的成员,以其对各种原生寄生虫(包括造成动物的共生虫病的寄生虫)的功效而著称;该物质具有广泛的活动,并经常用于治疗动物和宠物中Eimeria物种造成的感染;Ponazuril功能,通过阻止寄生虫中核酸合成最终导致其死亡;就物理特性而言,Ponazuril通常作为白色到非白色粉末,在有机溶剂中溶解,但在水中溶解作用有限;其安全性特征表明,其在建议的动物剂量中毒性较低,因此在兽医治疗中是一种首选;与任何制药剂一样,适当使用和遵守兽医准则对于确保功效和尽量减少潜在副作用至关重要.

结构式图片

欧盟法规

C&L通报

上下游产品

4-Hydroxyphenyltrifluoromethylsulphone

合成工艺路线路线简述

    4-(三氟甲基磺酰基)苯酚,1-(4-Bromo-3-Methylphenyl)-3-Methyl-1,3,5-Triazine-2,4,6-Trione置于n,N'-二([1,1'-联苯]-2-基)草酰胺,Potassium Tert-Butylate,Copper(I) Bromide体系中,用 乙腈 作为反应溶剂,化学反应 24.0H,以75.2%的收率获得产物妥曲珠利砜
    参考文献:帕托珠利和妥曲珠利的制备
    标题:帕托珠利和妥曲珠利的制备
    摘要:本发明涉及帕托珠利和妥曲珠利的制备,具体涉及1‑(4‑卤代‑3‑甲基苯基)‑3‑甲基‑1,3,5‑三嗪‑2,4,6‑三酮和对位取代的苯酚在铜催化剂/碱/添加物/溶剂存在条件下发生反应.该工艺操作简单,具有工业化放大生产前景.

    海关参考信息

    专利信息


    专利号:US-3625925-A
    优先权日:1967-09-06
    标题 :Synthesis of polythiol polymer intermediates from polyunsaturated hydrocarbons
    发明人:OSWALD ALEXIS A; MUELLER WOLFGANG H; HALL DANIEL N
    权利人:EXXON RESEARCH ENGINEERING CO
    摘要:Polythiols having more than two terminal and/or pendant thiol groups per polymer molecule are formed by the free radical catalyzed addition of a monomer system made up of either hydrogen sulfide or a dithiol alone or in combination with an acetylenic compound to a polyolefin having at least three olefin sites. The polyolefin is preferably a triterminal olefin. The polythiol products are liquid, essentially gel-free materials having number average molecular weights varying from 200 to 30,000. The polyfunctional prepolymers of the invention can be cured to stable three-dimensional networks with inexpensive bi-functional oxidants such as lead dioxide. Additionally, prepolymer compositions having 3 or more pendant or terminal thiol groups per molecule when combined with polyfunctional organic reagents, such as diepoxides, form stable, high-tenacity adhesive systems.

    专利号:US-3585184-A
    优先权日:1967-12-29
    标题 :2-amino - 2 - deoxy-d-glucopyrano-d-glucopyranans having the alpha-d-glucose configuration,method,and use
    发明人:WOLFROM MELVILLE L; WANG PAUL Y
    权利人:UNIV OHIO STATE
    摘要:2-AMINO-2-DEOXY - D - GLUCOPYRANO-D-GLUCOPYRANANS (BRIEFLY, 2-AMINO-2-DEOXY-AMYLOSES) HAVING THE ALPHA-DGLUCOSE CONFIGURATION AND METHOD OF PRODUCING SAME FROM AMYLOSE WITH RETENTION OF CONFIGURATION, INTERMEDIATES THEREFOR, AND USE THEREOF. AN ESPECIALLY VALUBLE UTILITY IS IN THE SYNTHESIS OF HEPARIN.

    专利号:CN-1534093-A
    优先权日:2003-03-28
    标 题:Synthesis of batroxobin gene and purification of its expression product

    专利号:CN-100335622-C
    优先权日:2003-03-28
    标 题:Synthesis of batroxobin gene and purification of its expression product

    专利号:CN-105507848-B
    优先权日:2015-12-17
    标 题 :The fast curable class of dehydration and organic synthesis class sealing agent compounding leak-blocking construction method

    专利号:CN-105507848-A
    优先权日:2015-12-17
    标 题:Construction method of fast dehydration curable type and organic synthesis type plugging agent compound plugging
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    主要参考文献


    1: Weerarathne P, Reichard M, Miller C, Scimeca RC. The Establishment of a Novel In Vitro System for Culturing Cytauxzoon felis. Pathogens. 2024 Jul 4;13(7):565. doi: 10.3390/pathogens13070565.
    2: Yuan Y, Yang L, Zhao Q, Xiong L, Yang M, Suo X, Hao Z. Ponazuril: Clinical efficacy, ultrastructure, and histopathology studies of in vivo anticoccidial action against Eimeria tenella. Vet Parasitol. 2024 Feb;326:110098. doi: 10.1016/j.vetpar.2023.110098. Epub 2023 Dec 18. 54(3):561-572. doi: 10.1638/2022-0091. 61(1):95-108. doi: 10.1177/03009858231179129. Epub 2023 Jun 12.
    9:1054417. doi: 10.3389/fvets.2022.1054417.

    合成参考文献


    摘要:d'ESAGUY A. [A letter from Ribeiro Sanches addressed to the Marquis de Pombal]. Scalpel (Brux). 1958 Sep 27;111(39):924–7.
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