2-(benzyloxy)thiophene | 37723-49-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-(benzyloxy)thiophene
• 英文别名: 2-Benzyloxy-thiophene；2-phenylmethoxythiophene
• CAS: 37723-49-2
• 化学式: C₁₁H₁₀OS
• 分子量: 190.266
• InChiKey: YRRQAJDSSFLMTO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  37.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(benzyloxy)thiophene 在 溶剂黄146 、 三氯氧磷 作用下， 以 甲醇 为溶剂， 反应 2.5h， 生成
  参考文献：
  名称：

  NOVEL P62 LIGAND COMPOUND, AND COMPOSITION CONTAINING SAME FOR PREVENTING, AMELIORATING, OR TREATING PROTEINOPATHIES

  摘要：

  Novel p62 ligand compounds, or a stereoisomer, a solvate, a hydrate, or a prodrug thereof are disclosed. The novel compounds, stereoisomer, solvate, hydrate, or prodrug activates selective autophagy in cells to selectively remove proteins, organelles, and coagulations in the body, and thus can be advantageously used as a pharmaceutical composition for preventing, ameliorating, or treating various proteinopathies. Compositions such as pharmaceutical composition or food compositions containing the novel p62 ligand compounds, stereoisomer, solvate, hydrate, or prodrug thereof as well as uses thereof are disclosed.

  公开号：

  US20220402873A1
• 作为产物：
  描述：

  2-碘噻吩 在 正丁基锂 、 copper(l) chloride 、 吡啶 作用下， 以 乙二醇二甲醚 、 正己烷 为溶剂， 反应 13.34h， 以9.5%的产率得到2-(benzyloxy)thiophene
  参考文献：
  名称：

  EP1782811

  摘要：

  公开号：

文献信息

• Facile preparation of thiophene C2-ethers using the Mitsunobu reaction
  作者：Craig S. Harris、Hervé Germain、Georges Pasquet

  DOI：10.1016/j.tetlet.2008.07.153

  日期：2008.10

  The preparation of thiophene ethers generally requires forcing conditions thus limiting the choice of alkyl substituent. Herein, we report the first successful generally applicable conditions for the selective O-alkylation of 2(5H)-thiophenone.

  噻吩醚的制备通常需要强制条件，因此限制了烷基取代基的选择。在这里，我们报道了2（5 H）-噻吩的选择性O-烷基化的第一个成功的普遍适用条件。
• [EN] AMINOPYRIMIDINE DERIVATIVES AND THEIR MEDICAL USE<br/>[FR] DERIVES DE 2-AMINOPYRIMIDINE ET LEUR APPLICATION EN MEDECINE
  申请人：NOVARTIS AG

  公开号：WO2004089913A1

  公开（公告）日：2004-10-21

  A compound of formula I or a pharmaceutically acceptable salt, ester or prodrug thereof wherein the variables haue the meanings as defined in the specification. Further disclosed are a method of inhibiting IKK activity using a compound of formula I, a method of inhibiting production of TNF using a compound of formula I, a compound of formula I for use as a pharmaceutical, a pharmaceutical composition comprising a compound of formula I, and use of a compound of formula I in the manufacture of a medicament for use as an immunosuppressant or anti-inflammatory agent.

  具有公式I的化合物或其药学上可接受的盐、酯或前药，其中变量的含义如规范中所定义。进一步披露了使用公式I的化合物抑制IKK活性的方法，使用公式I的化合物抑制TNF生成的方法，用于药用的公式I的化合物，包含公式I的化合物的药物组合物，以及使用公式I的化合物制造用作免疫抑制剂或抗炎药物的药物的用途。
• CYTOKINE PRODUCTION INHIBITORS, TRIAZEPINE COMPOUNDS, AND INTERMEDIATES THEREOF
  申请人：Japan Tobacco Inc.

  公开号：EP0934940A1

  公开（公告）日：1999-08-11

  The present invention relates to a cytokine production inhibitor comprising a compound of the formula [I] wherein R1 is aryl or heteroaryl; B is a group of the formula (a) or (b) wherein R2 is hydrogen atom, hydroxy, halogen atom and the like, R4 is hydrogen atom or halogen atom, or R2 and R4 in combination form carbonyl; R3 is lower alkoxy, cycloalkyl, aryl, heteroaryl, -X-Y and the like, wherein X is -(CH2)m-, -CO-, -COCH2-, -NHCH2-, -CH2NH-, -OCH2- and the like, Y is halogen atom, cycloalkyl, aryl or heteroaryl; R51 is -NHCONHR57 and the like; R52 is hydrogen atom or - COOR53; A is benzene ring or thiophene ring, novel triazepine compound and intermediates for the production of those triazepine compounds. The compounds of the formula [I] suppress production of cytokine such as IL-6, TNF-α, IL-8, IFNγ, IL-2, GM-CSF and the like, and are useful as cytokine production inhibitors or antiinflammatory drugs.

  本发明涉及一种细胞因子生产抑制剂，包括式[I]的化合物，其中R1为芳基或杂环基；B为式（a）或（b）的基团，其中R2为氢原子、羟基、卤原子等，R4为氢原子或卤原子，或R2和R4组成羰基；R3为较低的烷氧基、环烷基、芳基、杂环基、-X-Y等，其中X为-(CH2)m-、-CO-、-COCH2-、-NHCH2-、-CH2NH-、-OCH2-等，Y为卤原子、环烷基、芳基或杂环基；R51为-NHCONHR57等；R52为氢原子或-COOR53；A为苯环或噻吩环，以及用于生产这些三唑烷化合物的中间体。式[I]的化合物抑制细胞因子如IL-6、TNF-α、IL-8、IFNγ、IL-2、GM-CSF等的生产，可用作细胞因子生产抑制剂或抗炎药物。
• Novel antifungal agent containing heterocyclic compound
  申请人：Nakamoto Kazutaka

  公开号：US20070105943A1

  公开（公告）日：2007-05-10

  The present invention provides an antifungal agent represented by the formula: [wherein A 1 represents a 3-pyridyl group which may have a substituent, a quinolyl group which may have a substituent, or the like; X 1 represents a group represented by the formula —NH—C(═O)—, a group represented by the formula —C(═O)—NH—, or the like; E represents a furyl group, a thienyl group, a pyrrolyl group, a phenyl group, a pyridyl group, a tetrazolyl group, a thiazolyl group or a pyrazolyl group; with the proviso that A 1 may have 1 to 3 substituents, and E has one or two substituents].

  本发明提供了一种抗真菌剂，其表示为以下式子： [其中A1表示一个3-吡啶基团，可能具有取代基，喹啉基团，可能具有取代基或类似物；X1表示由公式—NH—C（═O）—，由公式—C（═O）—NH—或类似物表示的基团；E表示呋喃基团，噻吩基团，吡咯基团，苯基团，吡啶基团，四唑基团，噻唑基团或吡唑基团；但A1可能具有1到3个取代基，E具有一个或两个取代基。]
• Novel Antimalarial Agent Containing Heterocyclic Compound
  申请人：Nakamoto Kazutaka

  公开号：US20090227799A1

  公开（公告）日：2009-09-10

  Disclosed is an antimalarial agent containing a compound represented by the formula: [wherein A 1 represents a 3-pyridyl group that may have a substituent, a 6-quinolyl group that may have a substituent, or the like; X 1 represents a group represented by the formula —C(═O)—NH— or the like; E represents a furyl group, a thienyl group or a phenyl group; with the proviso that A 1 may have one to three substituents, and E has one of two substituents] or a salt thereof or hydrates thereof.

  揭示了一种抗疟疾剂，其包含由下式表示的化合物： [其中A1表示一个3-吡啶基团，可以有取代基，一个6-喹啉基团，可以有取代基或类似物；X1表示一个由公式-C（═O）-NH-或类似物表示的基团；E表示一个呋喃基团，噻吩基团或苯基团；但前提是A1可以有1到3个取代基，E有两个取代基之一]或其盐或水合物。