o-Aminophenylbenzoat | 721-48-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 缩酚酸和缩酚酸环醚类
• 英文名称: o-Aminophenylbenzoat
• 英文别名: O-Benzoyl-(2-amino-phenol)；Phenol, 2-amino-, 1-benzoate；(2-aminophenyl) benzoate
• CAS: 721-48-2
• 化学式: C₁₃H₁₁NO₂
• 分子量: 213.236
• InChiKey: NFPHUVYTLYGKPU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  52.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  o-Aminophenylbenzoat 在 ammonium hydroxide 作用下， 生成 2-(benzyloxy)-4-chloroaniline
  参考文献：
  名称：

  US1792156

  摘要：

  公开号：
• 作为产物：
  描述：

  苯甲酰氯 、 硝苯酚 在 chromium dichloride 、 锰 、 三甲基氯硅烷 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.25h， 生成 o-Aminophenylbenzoat
  参考文献：
  名称：

  Extending the Scope of Chromium−Manganese Redox-Coupled Reactions:  A One-Pot Synthesis of Benzoxazoles

  摘要：

  A critically important strategy for synthetic chemistry is the development of "domino" processes: those capable of concatenating multiple transformations into a single step. Such transformations not only provide an increase in synthetic efficiency, but also imply the development of a significant degree of mechanistic understanding. We report herein a new domino reaction, in which a chromium-manganese redox couple is employed both to catalytically reduce an o-hydroxy nitroarene and to oxidatively cyclize a subsequently formed imine. We find that the reaction is most effective for starting o-hydroxy nitroarenes with a strongly electron-withdrawing group at the para position.

  DOI：

  10.1021/jo005758f

文献信息

• Alkoxycarbonylamino benzoic acid or alkoxycarbonylamino tetrazolyl phenyl derivatives as IP antagonists
  申请人：——

  公开号：US20020165235A1

  公开（公告）日：2002-11-07

  This invention relates to compounds which are generally IP receptor antagonists and which are represented by Formula I: 1 wherein G 1 is selected from the group consisting of a, b 1 , and b 2 2 and A and G 2 are as defined in the specification; or individual isomers, racemic or non-racemic mixtures of isomers, or pharmaceutically acceptable salts or solvates thereof. The invention further relates to pharmaceutical compositions containing such compounds, methods for their use as therapeutic agents, and methods of preparation thereof.

  这项发明涉及一般为IP受体拮抗剂的化合物，其由以下式I表示： 其中G1选自a、b1和b2组成的群；A和G2如规范中定义；或其个别异构体、消旋或非消旋异构体混合物，或其药用可接受盐或溶剂。该发明还涉及含有这种化合物的药物组合物，以及它们作为治疗剂的使用方法和其制备方法。
• MUSCARINIC RECEPTOR AGONISTS, COMPOSITIONS, METHODS OF TREATMENT THEREOF, AND PROCESSES FOR PREPARATION THEREOF-176
  申请人：Jin Shujuan

  公开号：US20090221642A1

  公开（公告）日：2009-09-03

  Compounds of Formula 1, or pharmaceutically acceptable salts thereof: wherein X, R 1 , R 2 , R 3 , R 4 , R 5 , n, m, and p are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.

  式1的化合物，或其药用可接受的盐：其中X、R1、R2、R3、R4、R5、n、m和p的定义如规范中所述，以及包括这些化合物的盐和药物组合物已经准备好。它们在治疗中很有用，特别是在疼痛管理中。
• CURING AGENTS FOR EPOXY RESINS
  申请人：Dershem Stephen M

  公开号：US20130012620A1

  公开（公告）日：2013-01-10

  The present invention relates to curatives for epoxy resins, and compositions (e.g. adhesives) containing such resins cured using the same methods of preparation and uses therefor. More specifically, the present invention relates to hybrid curatives for epoxy resins comprising both aromatic amine, phenol and/or phenyl ester moieties. A further aspect of the current invention relates to new imidazole catalysts that possess a combination of excellent cure latency as well as low cure temperature onset.

  本发明涉及环氧树脂的硬化剂，以及含有经相同制备方法固化的这种树脂的组合物（例如胶粘剂）及其用途。更具体地，本发明涉及用于环氧树脂的混合硬化剂，包括芳香胺、酚和/或苯酯基团。本发明的另一个方面涉及具有优异固化潜伏期和低固化温度起始点的新咪唑催化剂。
• Design and synthesis of purine nucleoside analogues for the formation of stable anti-parallel-type triplex DNA with duplex DNA bearing the ^5mCG base pair
  作者：Ryotaro Notomi、Lei Wang、Shigeki Sasaki、Yosuke Taniguchi

  DOI：10.1039/d1ra02831f

  日期：——

  herein demonstrated for the first time the direct recognition of duplex DNA bearing the 5-methyl-2′-deoxycytosine and 2′-deoxyguanosine base pair by triplex DNA formation. Triplex-forming oligonucleotides contained the novel artificial nucleoside analogues 2-amino-2′-deoxy-nebularine derivatives, and their molecular design, synthesis, and functional evaluation are described.

  我们在此首次证明了通过三链 DNA 形成直接识别带有 5-甲基-2'-脱氧胞嘧啶和 2'-脱氧鸟苷碱基对的双链 DNA。三链体形成的寡核苷酸包含新型人工核苷类似物 2-氨基-2'-脱氧-nebularine 衍生物，并描述了它们的分子设计、合成和功能评估。
• Multicomponent Reactions of Convertible Isonitriles
  作者：Michael C. Pirrung、Subir Ghorai、Tannya R. Ibarra-Rivera

  DOI：10.1021/jo900414n

  日期：2009.6.5

  they are convertible). Moreover, they do not have the objectionable odors for which isonitriles are typically known, making them more accessible as reagents for organic synthesis. One focus of the work is isonitriles bearing perfluorinated alkyl groups that enable the ready separation of such reagents from nonfluorinated reaction products using the “light” fluorous method of fluorous solid-phase extraction

  通过恶唑的碱促进的开环制备了一个新的不饱和异腈家族，为常规的甲酰胺脱水途径提供了一种替代方法。这些化合物经历了已知的多官能团的多组分反应的全部补充，并提供了产生易于参与酰基取代反应的酰胺产物的理想特性（因此，它们是可转化的）。此外，它们不具有通常已知的异腈的令人讨厌的气味，这使得它们更易于用作有机合成的试剂。这项工作的重点之一是带有全氟烷基的异腈，可使用氟固相萃取的“轻型”氟方法将此类试剂从非氟化反应产物中轻松分离出来。