CAS: 78499-27-1; Bermoprofen

该化合物是一种属于丙酸化合物类的非类固醇抗炎药物,主要用于止痛和抗炎性特性,使其有效治疗疼痛,炎症和发烧等病症;该物质通过抑制环氧素酶(COX)的作用,在合成pleslandins,炎症和疼痛的调解者方面起着关键作用;Bermoprofen的特点是水溶性较低,可影响其生物利用率和体内吸收率;它通常是口服的,可存在于各种配方中,包括药片和胶囊;与其他非典ID一样,潜在的副作用可能包括胃肠道不适,心血管风险和肾损伤,特别是长期用途;使用者必须遵循有关准则,咨询保健专业人员,以减轻风险和确保安全使用.

结构式图片

MSDS等安全信息

合成工艺路线路线简述

  • 合成目标产物 Bermoprofen 主要起始原料 2-(4-(2-(Carboxymethyl)-4-Methylphenoxy)Phenyl)Propanoic Acid
  • (文献来源)合成步骤主要原料 2-(4-(2-(Carboxymethyl)-4-Methylphenoxy)Phenyl)Propanoic Acid
📜1-(2-碘-5-甲基苯基)乙-1-酮置于吡啶,硫酸,铜,Potassium Carbonate,Sulfur,溶剂黄146体系中,化学反应 14.5H,反应生成 化合物 T14546
参考文献:非甾体抗炎药.1. 10,11-二氢-11-氧二苯并[b,F]氧苯乙酸和相关化合物.
标题:非甾体抗炎药.1. 10,11-二氢-11-氧二苯并[b,F]氧苯乙酸和相关化合物.
摘要:
DOI:10.1021/jm00351A012

海关参考信息

专利信息


专利号:US-2012029226-A1
优先权日:2009-02-06
标题:Method for the synthesis of chiral alpha-aryl propionic acid derivatives
发明人:KAPTEIN BERNARDUS; VLIEG ELIAS; NOORDUIN WILLEM LIEUWE
权利人:KAPTEIN BERNARDUS; VLIEG ELIAS; NOORDUIN WILLEM LIEUWE
摘要:The present invention provides a method for the synthesis of optically pure α-aryl propionic acid derivatives comprising subjecting the corresponding racemic α-aryl propionic acid derivatives to high sheer or impact forces, such as grinding.

专利号:US-2024287041-A1
优先权日:2021-05-20
标题 :Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms
发明人:BALOGLU ERKAN; AUSTAD BRIAN C; ROE DAVID G; KEDUC ANDREW; GOTTSCHLING STEPHEN EDMUND; HECKER EVAN
权利人:KARYOPHARM THERAPEUTICS INC
摘要:The present invention relates to a method of preparing a compound represented by structural formula (VII), comprising reacting a compound represented by structural formula (II), with a compound represented by structural formula (III), in a solvent, in the presence of a Pd catalyst and one or more inorganic bases under conditions suitable to prepare a compound represented by structural formula (VII): The values and example values of the variables in structural formulas (VII), (II), and (III) are defined herein. The present invention also relates to crystalline Forms I and II of the compound represented by Structural Formula (VII), the use of the crystalline Forms in treating disease or disorders associated with CRM1 and method of preparing the crystalline Forms.

专利号:US-8143437-B2
优先权日:2002-02-19
标题:Methods for synthesis of prodrugs from 1-acyl-alkyl derivatives and compositions thereof
发明人:GALLOP MARK A; XIANG JIA-NING; YAO FENMEI; BHAT LAXMINARAYAN; ZHOU CINDY X
权利人:GALLOP MARK A; XIANG JIA-NING; YAO FENMEI; BHAT LAXMINARAYAN; ZHOU CINDY X; XENOPORT INC
摘要:The present invention provides a method for synthesizing 1-(acyloxy)-alkyl derivatives from 1-acyl-alkyl derivatives, which typically proceeds stereospecifically, in high yield, does not require the use of activated intermediates and/or toxic compounds and is readily amendable to scale-up. The current invention also provides 1-acyl-alkyl derivatives of known drug components and methods for synthesizing these 1-acyl-alkyl derivatives.

专利号:US-7309799-B2
优先权日:2004-06-01
标 题:Methods for the synthesis of milnacipran and congeners thereof
发明人:BUCHWALD STEPHEN L; SWAGER TIMOTHY M; RARIY ROMAN V
权利人:COLLEGIUM PHARMACEUTICAL INC
摘要:One aspect of the present invention relates to methods for synthesizing milnacipran or congeners thereof. Another aspect of the present invention relates to asymmetric methods for synthesizing enantiomerically enriched milnacipran or congeners thereof. The present invention also relates to methods for synthesizing intermediates useful in the non-asymmetric or asymmetric methods for synthesizing enantiomerically enriched milnacipran or congeners thereof.

专利号:AU-2022276509-A1
优先权日:2021-05-20
标题:Methods of synthesis of heteroaryl derivatives of triazolyl acrylamides and crystalline forms

专利号:US-9994558-B2
优先权日:2013-09-20
标题 :Multicyclic compounds and methods of using same
发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM; MCCAULEY DILARA; LANDESMAN YOSEF; GOLAN GALI; KALID ORI; SHECHTER SHARON
权利人:KARYOPHARM THERAPEUTICS INC
摘要:The invention generally relates to compounds represented by Structural Formula I: or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of structural formula I, or a pharmaceutically acceptable salt or composition thereof, e.g., in treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders (e.g., PAK-mediated, for example, PAK4-mediated, diseases and disorders).

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

主要参考文献


1: Mori M, Nakamura Y, Shirai Y, Seto Y, Nakamura H, Makita H, Imasato Y. Prolongation of antipyretic action and reduction of gastric ulcerogenicity in the rat by controlled-release granules of bermoprofen, a new nonsteroidal anti-inflammatory drug. J Pharm Sci. 1991 Sep;80(9):876-80. Japanese. Japanese. Japanese. Japanese.

合成参考文献


参考文献:10.1111/j.2042-7158.1985.tb04996.x
摘要:Nakamura H, Yokoyama Y, Motoyoshi S, Seto Y, Kadokawa T, Shimizu M. Inhibition of prostaglandin generation in the rabbit brain in-vivo by AD-1590, a non-steroidal anti-inflammatory agent with potent antipyretic activity. J Pharm Pharmacol. 1985 Dec;37(12):894–8. doi: 10.1111/j.2042-7158.1985.tb04996.x.
摘要:European Patent Application., #0003893
摘要:Yakuri to Chiryo. Pharmacology and Therapeutics., 16(2701), 1988
摘要:Journal of Medicinal Chemistry., 25(1065), 1982
摘要:Yakugaku Zasshi. Journal of Pharmacy., 108(788), 1988 []
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