4-三氟甲基-2-羟基喹啉 | 25199-84-2

• 物质功能分类: 医药中间体 - 杂环化合物 - 喹啉类化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 中文名称: 4-三氟甲基-2-羟基喹啉
• 中文别名: 4-三氟甲基-2(1H)-喹啉；2-羟基-4-三氟甲基喹啉
• 英文名称: 4-(trifluoromethyl)quinolin-2(1H)-one
• 英文别名: 4-trifluoromethyl-2(1H)-quinolinone；4-(trifluoromethyl)-1H-quinolin-2-one
• CAS: 25199-84-2
• 化学式: C₁₀H₆F₃NO
• 分子量: 213.159
• InChiKey: UUROBWTVZZNDFD-UHFFFAOYSA-N

物化性质

• 熔点：
  >240°C
• 沸点：
  284 ºC
• 密度：
  1.391
• 闪点：
  126 ºC

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  15
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  29.1
• 氢给体数：
  1
• 氢受体数：
  4

安全信息

• 安全说明：
  S24/25
• 海关编码：
  2933499090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H315,H319,H335

制备方法与用途

4-三氟甲基-2-羟基喹啉在药物领域有着广泛的应用，常作为抗菌、抗病毒、抗炎及抗肿瘤药物的重要中间体。

反应信息

• 作为反应物：
  描述：

  4-三氟甲基-2-羟基喹啉 在 palladium on activated charcoal 硫酸 、 氢气 、 硝酸 作用下， 反应 0.33h， 生成 6-氨基-4-三氟甲基喹啉-2-酮 2-羟基-4-三氟甲基-6-氨基喹啉
  参考文献：
  名称：

  Novel selective androgen receptor modulators: SAR studies on 6-bisalkylamino-2-quinolinones

  摘要：

  A series of selective androgen receptor modulators (SARMs) with a wide spectrum of receptor modulating activities was developed based on optimization of the 4-substituted 6-bisalkylamino-2-quinolinones (3). Significance of the trifluoromethyl group on the side chains and its interactions with amino acid residues within the androgen receptor (AR) ligand binding domain are discussed. A representative analog (9) was tested orally in a rodent model of hypogonadism and demonstrated desirable tissue selectivity. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.01.001
• 作为产物：
  描述：

  1-Isocyanato-2-(3,3,3-trifluoroprop-1-en-2-yl)benzene 以 氘代苯 为溶剂， 生成 4-三氟甲基-2-羟基喹啉
  参考文献：
  名称：

  Kinetic and Computational Studies of a Novel Pseudopericyclic Electrocyclization. The First Evidence for Torquoselectivity in a 6-π System

  摘要：

  DOI：

  10.1021/ja972701a

文献信息

• Compounds with anti-cancer activity
  申请人：Kawabe Takumi

  公开号：US20080275057A1

  公开（公告）日：2008-11-06

  Novel substituted azole diones are provided that kill cells, suppress cell proliferation, suppress cell growth, abrogate the cell cycle G2 checkpoint and/or cause adaptation to G2 cell cycle arrest. Methods of making and using the invention compounds are provided. The invention provides substituted azole diones to treat cell proliferation disorders. The invention includes the use of substituted azole diones to selectively kill or suppress cancer cells without additional anti-cancer treatment. The invention includes the use of cell cycle G2-checkpoint-abrogating substituted azole diones to selectively sensitize cancer cells to DNA damaging reagents, treatments and/or other types of anti-cancer reagents.

  提供了一种新型的取代咪唑二酮，可以杀死细胞，抑制细胞增殖，抑制细胞生长，废除细胞周期G2检查点和/或导致对G2细胞周期阻滞的适应。提供了制备和使用该发明化合物的方法。该发明提供了取代咪唑二酮来治疗细胞增殖紊乱。该发明包括使用取代咪唑二酮来选择性地杀死或抑制癌细胞，而无需额外的抗癌治疗。该发明包括使用细胞周期G2检查点废除的取代咪唑二酮来选择性地使癌细胞对DNA损伤试剂、治疗和/或其他类型的抗癌试剂产生敏感性。
• [EN] SUBSTITUTED AZOLE DIONE COMPOUNDS WITH ANTIVIRAL ACTIVITY<br/>[FR] COMPOSÉS AZOLE DIONE SUBSTITUÉS À ACTIVITÉ ANTIVIRALE
  申请人：STEMLINE THERAPEUTICS INC

  公开号：WO2021194954A1

  公开（公告）日：2021-09-30

  Provided herein are methods of using substituted azole dione compounds for treatment of viral infections.

  本文提供了使用替代咪唑二酮化合物治疗病毒感染的方法。
• [EN] COMPOUNDS FOR INHIBITION OF ALPHA 4β7 INTEGRIN<br/>[FR] COMPOSÉS POUR INHIBITION DE L'INTÉGRINE ALPHA 4β7
  申请人：GILEAD SCIENCES INC

  公开号：WO2020092401A1

  公开（公告）日：2020-05-07

  The present disclosure provides a compound of Formula (I); or a pharmaceutically acceptable salt thereof as described herein. The present disclosure also provides pharmaceutical compositions comprising a compound of Formula (I), processes for preparing compounds of Formula (I), and therapeutic methods for treating inflammatory disease.

  本公开提供一种如下所述的化合物的化学式(I)；或其药用可接受的盐。本公开还提供包括化合物的药物组合物的制备方法，制备化合物的方法和治疗炎症性疾病的治疗方法。
• Quinoline, tetrahydroquinoline and pyrimidine derivatives as mch antagonist
  申请人：Taisho Pharmaceutical Co. Ltd.

  公开号：EP1464335A3

  公开（公告）日：2007-05-09

  The present invention relates to compounds of the Formula (I) wherein Q is: which act as MCH receptor antagonists. These compositions are useful in pharmaceutical compositions whose use includes prophylaxis or treatment of improving memory function, sleeping and arousal, anxiety, depression, mood disorders, seizure, obesity, diabetes, appetite and eating disorders, cardiovascular disease, hypertension, dyslipidemia, myocardial infarction, binge eating disorders including bulimia, anorexia, mental disorders including manic depression, schizophrenia, delirium, dementia, stress, cognitive disorders, attention deficit disorder, substance abuse disorders and dyskinesias including Parkinson's disease, epilepsy, and addiction.

  这项发明涉及式(I)的化合物 其中Q是： 这些化合物作为MCH受体拮抗剂。这些组合物在制药组合物中的使用包括预防或治疗改善记忆功能、睡眠和觉醒、焦虑、抑郁、情绪障碍、癫痫、肥胖、糖尿病、食欲和进食障碍、心血管疾病、高血压、血脂异常、心肌梗死、暴食障碍，包括暴食症、厌食症、精神障碍，包括躁郁症、精神分裂症、谵妄、痴呆、压力、认知障碍、注意力缺陷障碍、物质滥用障碍和运动障碍，包括帕金森病、癫痫和成瘾症。
• Novel Sulfonaminoquinoline Hepcidin Antagonists
  申请人：Buhr Wilm

  公开号：US20120214803A1

  公开（公告）日：2012-08-23

  The present invention relates to novel hepcidin antagonists, pharmaceutical compositions comprising them and the use thereof as medicaments for the use in the treatment of iron metabolism disorders, such as, in particular, iron deficiency diseases and anemias, in particular anemias in connection with chronic inflammatory diseases.

  本发明涉及新型肝铁蛋白拮抗剂，包括它们的药物组合物以及将其用作药物治疗铁代谢紊乱，特别是铁缺乏病和贫血等疾病，特别是与慢性炎症性疾病相关的贫血。