methyl 2-hydroxy-4-(methoxymethoxy)-6-methylbenzoate | 1447922-63-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: methyl 2-hydroxy-4-(methoxymethoxy)-6-methylbenzoate
• 英文别名: Methyl 2-hydroxy-4-(methoxymethoxy)-6-methylbenzoate
• CAS: 1447922-63-5
• 化学式: C₁₁H₁₄O₅
• 分子量: 226.229
• InChiKey: SOTHDDUNRBVDGR-UHFFFAOYSA-N

物化性质

• 沸点：
  342.5±42.0 °C(Predicted)
• 密度：
  1?+-.0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  65
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  methyl 2-hydroxy-4-(methoxymethoxy)-6-methylbenzoate 在 potassium carbonate 、 potassium hydroxide 、 lithium diisopropyl amide 作用下， 以 甲醇 、 水 、 丙酮 为溶剂， 反应 60.5h， 生成 2-methoxy-4-(methoxymethoxy)-6-(pent-4-enyl)benzoic acid
  参考文献：
  名称：

  (3R,4S)-4-Hydroxylasiodiplodin 的首次全合成：一种简便的立体选择性方法

  摘要：

  (3R,4S)-4-hydroxylasiodiplodin 的第一个全合成描述了从乙酰乙酸甲酯和常用的碳水化合物，d-甘露醇开始，d-甘露醇经常用于有机合成。简便的立体选择性方法涉及作为关键步骤的 Barbier 烯丙基化和闭环复分解。

  DOI：

  10.1055/s-0032-1317805
• 作为产物：
  描述：

  2,4-二羟基-6-甲基苯甲酸 在 4-二甲氨基吡啶 、 氯化亚砜 、 N,N-二异丙基乙胺 作用下， 以 乙二醇二甲醚 、 二氯甲烷 为溶剂， 反应 24.0h， 生成 methyl 2-hydroxy-4-(methoxymethoxy)-6-methylbenzoate
  参考文献：
  名称：

  6-Oxomethylidenecyclohexa-2,4-diene-1-one衍生物与各种亲核试剂的产生和捕集的光解研究

  摘要：

  α-Oxoketenes和环己二烯α - oxoketenes是反应性的中间体，尤其是后者，由于它们的高再芳构化的潜力。在这篇通讯中，我们报告了从 4-OMe 和 4-OMOM 保护的间苯二酸二恶英产生此类物质的光解研究，以及它们的捕获以产生间苯二酸酯和酰胺，以及与烯醇-醚作为捕获试剂的加合物的形成。

  DOI：

  10.1002/hlca.202100189

文献信息

• [EN] NADPH OXIDASE INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE LA NADPH OXYDASE ET LEUR UTILISATION
  申请人：UNIV EMORY

  公开号：WO2019023448A1

  公开（公告）日：2019-01-31

  This disclosure relates to compounds and methods of treating or preventing a Nox related disease or condition comprising administering to a subject in need thereof a Nox inhibitor or pharmaceutical compositions comprising a Nox inhibitor disclosed herein, derivatives, or compounds disclosed herein optionally substituted with one or more substitutes including optional salt and prodrug forms. In certain embodiments, this disclosure relates to sulfonylurea compounds and uses reported herein.

  本公开涉及化合物和治疗或预防与Nox相关的疾病或症状的方法，包括向需要的受试者施用本公开披露的Nox抑制剂或含有本公开披露的Nox抑制剂、衍生物或化合物的药物组合物，该药物组合物可选择地用一个或多个替代物替代，包括可选的盐和前药形式。在某些实施例中，本公开涉及磺酰脲化合物和此处报告的用途。
• NADPH oxidase inhibitors and uses thereof
  申请人：Emory University

  公开号：US11236053B2

  公开（公告）日：2022-02-01

  This disclosure relates to compounds and methods of treating or preventing a Nox related disease or condition comprising administering to a subject in need thereof a Nox inhibitor or pharmaceutical compositions comprising a Nox inhibitor disclosed herein, derivatives, or compounds disclosed herein optionally substituted with one or more substitutes including optional salt and prodrug forms. In certain embodiments, this disclosure relates to sulfonylurea compounds and uses reported herein.

  本公开涉及治疗或预防与Nox相关的疾病或病症的化合物和方法，包括向有需要的受试者施用Nox抑制剂或药物组合物，其中包含本文公开的Nox抑制剂、衍生物或本文公开的化合物，可任选被一种或多种替代物取代，包括任选的盐和原药形式。在某些实施方案中，本公开涉及本文所报道的磺酰脲化合物及其用途。
• Rh-Catalyzed Cyclization of 3-Aryloxycarbonyldiazonaphthoquinones for the Synthesis of β-Phenylnaphthalene Lactones and Formal Synthesis of Pradimicinone
  作者：Mitsuru Kitamura、Shuhei Takahashi、Tatsuo Okauchi

  DOI：10.1021/acs.joc.5b01251

  日期：2015.8.21

  In this study, we developed a novel method for the synthesis of beta-phenylnaphthalene lactones. The diazo-transfer reactions of 2-azido-1,3-dimethylimidazolinium chlorides to 3-aryloxycarbonyl-1-naphthols proceeded smoothly to give corresponding 3-aryloxycarbonyldiazonaphthoquinones in high yields. These intermediates were further transformed to beta-phenylnaphthalene lactones through a Rh-catalyzed intramolecular formal C-H insertion reaction. This method of lactone formation was efficiently applied to the formal total synthesis of pradimicinone.
• Design, synthesis, and biological evaluation of inhibitors of the NADPH oxidase, Nox4
  作者：Qian Xu、Amol A. Kulkarni、Ayyiliath M. Sajith、Dilbi Hussein、David Brown、Osman F. Güner、M. Damoder Reddy、E. Blake Watkins、Bernard Lassègue、Kathy K. Griendling、J. Phillip Bowen

  DOI：10.1016/j.bmc.2017.12.023

  日期：2018.3

  NADPH oxidases (Nox enzymes) are critical mediators of both physiologic and pathophysiologic processes. Nox enzymes catalyze NADPH-dependent generation of reactive oxygen species (ROS), including superoxide and hydrogen peroxide. Until recently, Nox4 was proposed to be involved exclusively in normal physiologic functions. Compelling evidence, however, suggests that Nox4 plays a critical role in fibrosis, as well as a host of pathologies and diseases. These considerations led to a search for novel, small molecule inhibitors of this important enzyme. Ultimately, a series of novel tertiary sulfonylureas (23-25) was designed using pharmacophore modeling, synthesized, and evaluated for inhibition of Nox4-dependent signaling. (C) 2017 Elsevier Ltd. All rights reserved.
• NADPH Oxidase Inhibitors and Uses Thereof
  申请人：Emory University

  公开号：US20200270214A1

  公开（公告）日：2020-08-27

  This disclosure relates to compounds and methods of treating or preventing a Nox related disease or condition comprising administering to a subject in need thereof a Nox inhibitor or pharmaceutical compositions comprising a Nox inhibitor disclosed herein, derivatives, or compounds disclosed herein optionally substituted with one or more substitutes including optional salt and prodrug forms. In certain embodiments, this disclosure relates to sulfonylurea compounds and uses reported herein.