methyl 4-(((4-(trifluoromethoxy)phenyl)amino)methyl)benzoate | 643013-13-2

• 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 4-(((4-(trifluoromethoxy)phenyl)amino)methyl)benzoate
• 英文别名: 4-[(4-trifluoromethoxyphenylamino)methyl]benzoic acid methyl ester；methyl 4-[[4-(trifluoromethoxy)anilino]methyl]benzoate
• CAS: 643013-13-2
• 化学式: C₁₆H₁₄F₃NO₃
• 分子量: 325.287
• InChiKey: HBUQYDLRVPIHTH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.4
• 重原子数：
  23
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  47.6
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  methyl 4-(((4-(trifluoromethoxy)phenyl)amino)methyl)benzoate 在 lithium aluminium tetrahydride 、 氢溴酸 、 sodium hydride 、 sodium cyanoborohydride 、 溶剂黄146 作用下， 以 乙醚 、 乙醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 22.25h， 生成 N-methyl-N-[4-({[(6S)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b]-[1,3]oxazin-6-yl]oxy}methyl)benzyl]-4-(trifluoromethoxy)aniline
  参考文献：
  名称：

  Synthesis and Structure–Activity Relationships for Extended Side Chain Analogues of the Antitubercular Drug (6S)-2-Nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine (PA-824)

  摘要：

  Novel extended side chain nitroimidazooxazine analogues featuring diverse linker groups between two aryl rings were studied as a potential strategy to improve solubility and oral activity against chronic infection by Mycobacterium tuberculosis. Both lipophilic and highly polar functionalities (e.g., carboxamide, alkylamine, piperazine, piperidine, but not sulfonamide) were well tolerated in vitro, and the hydrophilic linkers provided some solubility improvements, particularly in combination with pyridine rings. Most of the 18 compounds further assessed showed high microsomal stabilities, although in the acute infection mouse model, just one stilbene (6-fold) and two pyridine-containing acetylene derivatives (5-fold and >933-fold) gave in vivo efficacies notably superior to the clinical stage compound pretomanid (PA-824). The most efficacious analogue also displayed outstanding in vivo activity in the stringent chronic model (up to 24-fold better than the drug delamanid and 4-fold greater than our previous best phenylpyridine candidate), with favorable pharmacokinetics, including good oral bioavailability in the rat.

  DOI：

  10.1021/jm501608q
• 作为产物：
  描述：

  4-溴甲基苯甲酸甲酯 、 对三氟甲氧基苯胺 在 N,N-二异丙基乙胺 作用下， 以 乙腈 为溶剂， 反应 16.0h， 以42.8%的产率得到methyl 4-(((4-(trifluoromethoxy)phenyl)amino)methyl)benzoate
  参考文献：
  名称：

  [EN] NOVEL COMPOUNDS FOR SELECTIVE HISTONE DEACETYLASE INHIBITORS, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
  [FR] NOUVEAUX COMPOSÉS POUR INHIBITEURS SÉLECTIFS D'HISTONE DÉSACÉTYLASES ET COMPOSITION PHARMACEUTIQUE LES COMPRENANT

  摘要：

  本发明涉及新型尿素衍生物，更特别地涉及具有组蛋白去乙酰化酶（HDAC）抑制活性的新型尿素衍生物，其异构体，其药学上可接受的盐，它们用于制备包含相同成分的药物的用途，包含相同成分的药物组合物，使用该组合物的治疗方法，以及制备新型尿素衍生物的方法。作为选择性组蛋白去乙酰化酶（HDAC）抑制剂的新型尿素衍生物对于治疗组蛋白去乙酰化酶介导的疾病，如恶性肿瘤、炎症性疾病、类风湿性关节炎、神经退行性疾病等非常有效。

  公开号：

  WO2014178606A1

文献信息

• [EN] NOVEL GLUCAGON ANTAGONISTS/INVERSE AGONISTS<br/>[FR] NOUVEAUX ANTAGONISTES/AGONISTES INVERSES DU GLUCAGON
  申请人：NOVO NORDISK AS

  公开号：WO2004002480A1

  公开（公告）日：2004-01-08

  Novel compounds that act to antagonize the action of the glucagon peptide hormone on the glucagon receptor. More particularly, it relates to glucagon antagonists or inverse agonists.

  新型化合物，用于拮抗胰高血糖素肽激素对胰高血糖素受体的作用。更具体地说，这涉及胰高血糖素拮抗剂或逆向激动剂。
• Novel glucagon antagonists/inverse agonists
  申请人：Lau Jesper

  公开号：US20050256175A1

  公开（公告）日：2005-11-17

  Novel compounds that act to antagonize the action of the glucagon peptide hormone on the glucagon receptor. More particularly, it relates to glucagon antagonists or inverse agonists.

  这是一种新型化合物，可以对抗胰高血糖素肽激素在胰高血糖素受体上的作用。更具体地说，它涉及到胰高血糖素拮抗剂或反向激动剂。
• NOVEL COMPOUNDS FOR SELECTIVE HISTONE DEACETYLASE INHIBITORS, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
  申请人：CHONG KUN DANG PHARMACEUTICAL CORP.

  公开号：US20160083354A1

  公开（公告）日：2016-03-24

  The present invention relates to novel urea derivatives and, more particularly, to novel urea derivatives with histone deacetylase (HDAC) inhibitory activity, isomers thereof, pharmaceutically acceptable salts thereof, their use for the preparation of a medicaments comprising the same, a pharmaceutical composition comprising the same, a treatment method using the composition, and a method for preparing novel urea derivatives. The novel urea derivatives as selective histone deacetylase (HDAC) inhibitors are effective for the treatment of histone deacetylase-mediated diseases such as malignant tumors, inflammatory diseases, rheumatoid arthritis, neurodegeneration, etc.

  本发明涉及新型尿素衍生物，更具体地涉及具有组蛋白去乙酰化酶（HDAC）抑制活性的新型尿素衍生物、其异构体、其药学上可接受的盐、用于制备包括它们的药物的使用、包括它们的制药组合物、使用该组合物的治疗方法和制备新型尿素衍生物的方法。这些新型尿素衍生物作为选择性组蛋白去乙酰化酶（HDAC）抑制剂对组蛋白去乙酰化酶介导的疾病，如恶性肿瘤、炎症性疾病、类风湿性关节炎、神经退行性疾病等具有治疗作用。
• Human Glucagon Receptor Antagonists with Thiazole Cores. A Novel Series with Superior Pharmacokinetic Properties
  作者：Peter Madsen、János T. Kodra、Carsten Behrens、Erica Nishimura、Claus B. Jeppesen、Lone Pridal、Birgitte Andersen、Lotte B. Knudsen、Carmen Valcarce-Aspegren、Mette Guldbrandt、Inge T. Christensen、Anker S. Jørgensen、Lars Ynddal、Christian L. Brand、Morten Aa. Bagger、Jesper Lau

  DOI：10.1021/jm8016249

  日期：2009.5.14

  The aim of the work presented here was to design and synthesize potent human glucagon receptor antagonists with improved pharmacokinetic (PK) properties for development of pharmaceuticals for the treatment of type 2 diabetes. We describe the preparation of compounds with cyclic cores (5-aminothiazoles), their binding affinities for the human glucagon and GIP receptors, as well as affinities for rat, mouse, pig, dog, and monkey glucagon receptors. Generally, the compounds had slightly less glucagon receptor affinity compared to compounds of the previous series, but this was compensated for by much improved PK profiles in both rats and dogs with high oral bioavailabilities and sustained high plasma exposures. The compounds generally showed species selectivity for glucagon receptor binding with poor affinities for the rat, mouse, rabbit, and pig receptors. However, dog and monkey glucagon receptor affinities seem to reflect the human situation. One compound of this series, 18, was tested intravenously in an anesthetized glucagon-challenged monkey model of hyperglucagonaemia and hyperglycaemia and was shown dose-dependently to decrease glycaemia. Further, high plasma exposures and a long plasma half-life (5.2 h) were obtained.
• NOVEL GLUCAGON ANTAGONISTS/INVERSE AGONISTS
  申请人：NOVO NORDISK A/S

  公开号：EP1519723A1

  公开（公告）日：2005-04-06