N-(4-fluorophenyl)-2-naphthalenecarboxamide | 300402-71-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: N-(4-fluorophenyl)-2-naphthalenecarboxamide
• 英文别名: N-(4-fluorophenyl)-2-naphthamide；N-(4-fluorophenyl)naphthalene-2-carboxamide
• CAS: 300402-71-5
• 化学式: C₁₇H₁₂FNO
• 分子量: 265.287
• InChiKey: AZJHJQPKYMVIPC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  N-苯基萘-2-甲酰胺 在 二(叔丁基羰基氧基)碘苯 、 氟化氢吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 12.0h， 以13%的产率得到N-(4-fluorophenyl)-2-naphthalenecarboxamide
  参考文献：
  名称：

  Hypervalent Iodine Mediated para-Selective Fluorination of Anilides

  摘要：

  A metal-free method for the direct regioselective fluorination of anilides has been developed. In the presence of bis(tert-butylcarbonyloxy)iodobenzene (PhI(OPiv)(2)) and hydrogen fluoride-pyridine, the para-fluorination products of anilides were obtained in moderate to good yields. Because of its operational safety and the use of readily available reagents, this new procedure provides facile access to a variety of para-fluorinated anilides.

  DOI：

  10.1021/jo302099d

文献信息

• One-pot mechanosynthesis of aromatic amides and dipeptides from carboxylic acids and amines
  作者：Vjekoslav Štrukil、Boris Bartolec、Tomislav Portada、Ivica Đilović、Ivan Halasz、Davor Margetić

  DOI：10.1039/c2cc36613d

  日期：——

  Environmentally friendly one-pot synthesis of amides, bis-amides and dipeptides by mechanochemical carbodiimide-mediated coupling of carboxylic acids and amines is described; high reaction yields and simple aqueous work-up allow for the clean, practical and fast preparation of a variety of compounds containing the amide bond from readily accessible reagents.

  通过机械化学碳二亚胺介导的羧酸和胺的偶联，描述了环境友好的一锅合成酰胺，双酰胺和二肽。高反应产率和简单的水后处理使得可以从容易获得的试剂中清洁，实用，快速地制备各种含有酰胺键的化合物。
• Investigating the Spectrum of Biological Activity of Substituted Quinoline-2-Carboxamides and Their Isosteres
  作者：Tomas Gonec、Pavel Bobal、Josef Sujan、Matus Pesko、Jiahui Guo、Katarina Kralova、Lenka Pavlacka、Libor Vesely、Eva Kreckova、Jiri Kos、Aidan Coffey、Peter Kollar、Ales Imramovsky、Lukas Placek、Josef Jampilek

  DOI：10.3390/molecules17010613

  日期：——

  In this study, a series of thirty-five substituted quinoline-2-carboxamides and thirty-three substituted naphthalene-2-carboxamides were prepared and characterized. They were tested for their activity related to the inhibition of photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts. Primary in vitro screening of the synthesized compounds was also performed against four mycobacterial species. N-Cycloheptylquinoline-2-carboxamide, N-cyclohexylquinoline-2-carboxamide and N-(2-phenylethyl)quinoline-2-carboxamide showed higher activity against M. tuberculosis than the standards isoniazid or pyrazinamide and 2-(pyrrolidin-1-ylcarbonyl)quinoline and 1-(2-naphthoyl)pyrrolidine expressed higher activity against M. kansasii and M. avium paratuberculosis than the standards isoniazid or pyrazinamide. The most effective antimycobacterial compounds demonstrated insignificant toxicity against the human monocytic leukemia THP-1 cell line. The PET-inhibiting activity expressed by IC50 value of the most active compound N-benzyl-2-naphthamide was 7.5 μmol/L. For all compounds, the structure-activity relationships are discussed.

  本研究制备并鉴定了一系列 35 种取代的喹啉-2-羧酰胺和 33 种取代的萘-2-羧酰胺。对它们抑制菠菜叶绿体光合电子传递（PET）的活性进行了测试。还对合成的化合物进行了针对四种霉菌的体外初筛。N-环庚基喹啉-2-甲酰胺、N-环己基喹啉-2-甲酰胺和 N-(2-苯基乙基)喹啉-2-甲酰胺对结核杆菌的活性高于标准异烟肼。与标准异烟肼或吡嗪酰胺相比，N-环己基喹啉-2-甲酰胺和 N-(2-苯基乙基)喹啉-2-甲酰胺对结核杆菌的活性更高；与标准异烟肼或吡嗪酰胺相比，2-(吡咯烷-1-羰基)喹啉和 1-(2-萘甲酰基)吡咯烷对堪萨斯疫霉菌和副结核杆菌的活性更高。最有效的抗霉菌化合物对人类单核细胞白血病 THP-1 细胞系的毒性很小。最有效化合物 N-苄基-2-萘甲酰胺的 PET 抑制活性（以 IC50 值表示）为 7.5 μmol/L。本文讨论了所有化合物的结构-活性关系。
• Highly Chemoselective Transamidation of Unactivated Tertiary Amides by Electrophilic N−C(O) Activation by Amide‐to‐Acyl Iodide Re‐routing
  作者：Dongxu Zuo、Qun Wang、Long Liu、Tianzeng Huang、Michal Szostak、Tieqiao Chen

  DOI：10.1002/anie.202202794

  日期：2022.6.13

  The challenging transamidation of unactivated tertiary amides using equivalent amounts of amines has been accomplished via cooperative acid/iodide catalysis. The method provides a novel manifold to re-route the reactivity of unactivated and unreactive N,N-dialkyl amides through reactive acyl iodide intermediates, representing a powerful new activation mode of unactivated amide bonds.

  使用等量的胺对未活化的叔酰胺进行具有挑战性的转酰胺化反应是通过协同酸/碘化物催化完成的。该方法提供了一种新的方法，通过反应性酰碘中间体重新引导未活化和未反应性N,N-二烷基酰胺的反应性，代表了一种强大的未活化酰胺键的新活化模式。
• Amide-based inhibitors of p38α MAP kinase. Part 1: Discovery of novel N-pyridyl amide lead molecules
  作者：Gregory R. Luedtke、Kurt Schinzel、Xuefei Tan、Richland W. Tester、Imad Nashashibi、Yong-jin Xu、Sundeep Dugar、Daniel E. Levy、Joon Jung

  DOI：10.1016/j.bmcl.2010.02.088

  日期：2010.4

  A novel series of N-pyridyl amides as potent p38 alpha kinase inhibitors is described. Based on the structural similarities between the initial hit and a well-known imidazole pyrimidine series of p38 alpha inhibitors, potencies within the newly discovered series were quickly improved by installation of an (S)-alpha-methylbenzyl moiety at the 2-position of the pyridine ring. The proposed binding modes of the new series to p38 alpha were evaluated against SAR findings and provided rationale for further development of this series of molecules. (C) 2010 Elsevier Ltd. All rights reserved.