CAS: 13669-70-0; 5-Methyl-1-Phenyl-3,4,5,6-Tetrahydro-1H-Benzo[f][1,4]Oxazocine

该化合物是一种环环环化合物,其核心为苯氧辛基,由于其结构复杂性和潜在的生物活动,对药用化学和药物研究很感兴趣.八人环系系统中的氮原子和氧原子的存在为进一步功能化提供了多种用途,使其成为合成应用中有价值的中间体.其硬脚架可能有助于选择性的约束性特性,特别是在CNS目标......

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CAS号23327-57-3 盐酸奈福泮 | CAS号18409-76-2 2-(1-苯基-2,3-二氢-... | CAS号84940-28-3 1-苯基-3,4,5,6-四氢... | CAS号865-50-9 氘代碘甲烷

合成工艺路线路线简述

    📜盐酸奈福泮置于碳酸氢钠体系中,用 水 用作溶剂,以99%的收率获得奈福泮
    参考文献: Malodor Counteracting Composition And Agent And The Use Thereof[fr] Composition Et Agent Contre Les Mauvaises Odeurs Et Utilisation Associée
    标题: Malodor Counteracting Composition And Agent And The Use Thereof[fr] Composition Et Agent Contre Les Mauvaises Odeurs Et Utilisation Associée
    摘要:本发明涉及一种消除异味的组合物.具体而言,本发明涉及一种包含奈福泮,其多晶形态,水合物或溶剂化物的消除异味组合物.本发明还涉及所述组合物的使用和减弱或抑制剂,用于减弱或抑制异味,特别是土壤,潮湿和/或发霉异味.

    海关参考信息

    专利信息


    专利号:US-7576211-B2
    优先权日:2004-09-30
    标题 :Synthesis of thienopyridinone compounds and related intermediates
    发明人:DHANOA DALE S; BECKER OREN; NOIMAN SILVIA; CHEN DONGLI; MARANTZ YAEL; SHACHAM SHARON; HEIFETZ ALEXANDER; INBAL BOAZ; BAR-HAIM SHAY; MOHANTY PRADYUMNA; LOBERA MERCEDES; WU LAURENCE
    权利人:EPIX DELAWARE INC
    摘要:The invention relates to 5-HT receptor agonists and partial agonists. Novel thienopyridinone compounds represented by Formula I, and synthesis and uses thereof for treating diseases mediated directly or indirectly by 5-HT receptors, are disclosed. Such conditions include Alzheimer's disease, cognition disorders, irritable bowel syndrome, nausea, emesis, vomiting, prokinesia, gastroesophageal reflux disease, nonulcer dyspepsia, depression, anxiety, urinary incontinence, migraine, arrhythmia, atrial fibrillation, ischemic stroke, gastritis, gastric emptying disorders, feeding disorders, gastrointestinal disorders, constipation, erectile dysfunction, and respiratory depression. Methods of preparation and novel intermediates and pharmaceutical salts thereof are also included.

    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-2008214827-A1
    优先权日:2004-02-03
    标 题:Synthesis of Cyanoimino-Benzoimidazoles
    发明人:GOEHRING R RICHARD; WHITEHEAD JOHN; SHAO BIN
    权利人:EURO CELTIQUE SA
    摘要:Disclosed in certain embodiments is a process for synthesizing a compound of formula (V) and salts 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).

    专利号:US-2006084805-A1
    优先权日:2004-09-30
    标题:Synthesis of thienopyridinone compounds and related intermediates

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Girard P, Chauvin M, Verleye M. Nefopam analgesia and its role in multimodal analgesia: A review of preclinical and clinical studies. Clin Exp Pharmacol Physiol. 2016 Jan;43(1):3-12. doi: 10.1111/1440-1681.12506. 2006–. Nefopam. 2018 Dec 3.
    13:323-329. doi: 10.2147/JPR.S224478.
    4: Pasutharnchat K, Wichachai W, Buachai R. Analgesic efficacy of nefopam for cancer pain: a randomized controlled study. F1000Res. 2020 May 19;9:378. doi: 10.12688/f1000research.23455.1.

    合成参考文献


    参考文献:10.1007/s12630-011-9554-y
    摘要:Le Corre F, Nejmeddine S, Fatahine C, Tayar C, Marty J, Plaud B. Recurarization after sugammadex reversal in an obese patient. Journal canadien d'anesthésie. 2011 Jul 13;58(10):944. doi: 10.1007/s12630-011-9554-y.
    参考文献:10.1093/toxsci/kfj064
    摘要:Pérez-Gómez A, Ferrero-Gutierrez A, Novelli A, Franco JM, Paz B, Fernández-Sánchez MT. Potent neurotoxic action of the shellfish biotoxin yessotoxin on cultured cerebellar neurons. Toxicol Sci. 2006 Mar;90(1):168–77. doi: 10.1093/toxsci/kfj064.
    参考文献:10.1002/elps.201000630
    摘要:Yu T, Du Y, Chen B. Evaluation of clarithromycin lactobionate as a novel chiral selector for enantiomeric separation of basic drugs in capillary electrophoresis. Electrophoresis. 2011 Jul;32(14):1898–905. doi: 10.1002/elps.201000630.
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