4-羟基-8-三氟甲基喹啉-3-甲酸 | 23779-95-5

• 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-羟基-8-三氟甲基喹啉-3-甲酸
• 中文别名: 4-羟基-8-三氟甲基喹啉-3-羧酸
• 英文名称: 4-hydroxy-8-(trifluoromethyl)quinoline-3-carboxylic acid
• 英文别名: 4-hydroxy-8-trifluoromethylquinoline-3-carboxylic acid；4-hydroxy-8-trifluoromethyl-quinoline-3-carboxylic acid；4-hydroxy-8-trifluoromethyl-3-quinoline-carboxylic acid；4-hydroxy-8-trifluoromethyl-3-quinolinecarboxylic acid；3-Carboxy-4-hydroxy-8-trifluormethyl-chinolin；4-oxo-8-(trifluoromethyl)-1H-quinoline-3-carboxylic acid
• CAS: 23779-95-5
• 化学式: C₁₁H₆F₃NO₃
• mdl: MFCD00047603
• 分子量: 257.169
• InChiKey: GQZVPBYGGIQINZ-UHFFFAOYSA-N

物化性质

• 熔点：
  292 °C(Solv: acetone (67-64-1))
• 沸点：
  380.3±42.0 °C(Predicted)
• 密度：
  1.594±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  66.4
• 氢给体数：
  2
• 氢受体数：
  7

安全信息

• 危险等级：
  IRRITANT
• 危险品标志：
  Xi
• 海关编码：
  2933499090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 4-Hydroxy-8-(trifluoromethyl)quinoline-3-carboxylic acid
Synonyms:

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

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Section 3. Composition/information on ingredients.
Ingredient name: 4-Hydroxy-8-(trifluoromethyl)quinoline-3-carboxylic acid
CAS number: 23779-95-5

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Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

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Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

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Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

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Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

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Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

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Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C11H6F3NO3
Molecular weight: 257.2

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Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, nitrogen oxides, hydrogen fluoride.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

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Section 14. Transportation information
Non-harzardous for air and ground transportation.

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Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  4-羟基-8-三氟甲基喹啉-3-甲酸 在 三氯氧磷 作用下， 反应 20.42h， 生成 4-氯-8-(三氟甲基)喹啉
  参考文献：
  名称：

  对恶性疟原虫疟疾具有高效力的不对称双喹啉

  摘要：

  在现代药物开发的历史中，基于喹啉的支架一直是抗疟药物的中流砥柱，包括许多青蒿素联合疗法 (ACTs)。尽管在寻找新型抗疟支架方面取得了很大进展，但喹啉可能仍然有用，特别是如果发现了此类非常有效的化合物。我们在此报告了结构-活性关系 (SAR) 研究的结果，该研究评估了潜在的不对称双喹啉抗疟原虫药物候选物，该研究使用针对细胞培养中完整寄生虫的体外活性。发现许多不对称双喹啉对氯喹敏感和对氯喹具有抗性的恶性疟原虫寄生虫均具有高度效力。

  DOI：

  10.3390/molecules25092251
• 作为产物：
  描述：

  邻氨基三氟甲苯 在 对甲苯磺酸 、 sodium hydroxide 作用下， 以 苯 为溶剂， 反应 25.5h， 生成 4-羟基-8-三氟甲基喹啉-3-甲酸
  参考文献：
  名称：

  对恶性疟原虫疟疾具有高效力的不对称双喹啉

  摘要：

  在现代药物开发的历史中，基于喹啉的支架一直是抗疟药物的中流砥柱，包括许多青蒿素联合疗法 (ACTs)。尽管在寻找新型抗疟支架方面取得了很大进展，但喹啉可能仍然有用，特别是如果发现了此类非常有效的化合物。我们在此报告了结构-活性关系 (SAR) 研究的结果，该研究评估了潜在的不对称双喹啉抗疟原虫药物候选物，该研究使用针对细胞培养中完整寄生虫的体外活性。发现许多不对称双喹啉对氯喹敏感和对氯喹具有抗性的恶性疟原虫寄生虫均具有高度效力。

  DOI：

  10.3390/molecules25092251

文献信息

• Quinolines useful in treating cardiovascular disease
  申请人：Collini D. Michael

  公开号：US20050131014A1

  公开（公告）日：2005-06-16

  This invention provides compounds of formula I that are useful in the treatment or inhibition of LXR mediated diseases.

  本发明提供了式I化合物的用途，它们在治疗或抑制LXR介导的疾病中是有用的。
• 4-Hydroxy-3-quinolinecarboxamides with antiarthritic and analgesic activities
  作者：Francois Clemence、Odile Le Martret、Francoise Delevallee、Josette Benzoni、Alain Jouanen、Simone Jouquey、Michel Mouren、Roger Deraedt

  DOI：10.1021/jm00402a034

  日期：1988.7

  by the oral route as antiinflammatory agents in carrageenin-induced foot edema and adjuvant-induced arthritis and as analgesic agents in the acetic acid induced writhing test. Among the most active molecules, some have shown both analgesic and acute antiinflammatory activities. Others, such as compounds 24, 37, and 52, were only powerful peripherally acting analgesics. Compound 52, being active at 1

  已经合成了一系列的4-羟基-3-喹啉甲酰胺，并通过口服途径评价了角叉菜胶引起的足部水肿和佐剂引起的关节炎中的抗炎药，以及乙酸引起的扭体试验中的镇痛药。在最活跃的分子中，有些已经显示出止痛和急性抗炎活性。其他化合物，例如化合物24、37和52，仅是有效的外周镇痛药。活性为1 mg / kg（ED50）的化合物52是该系列中最有效的化合物。一些在2位上被醇，酯或胺官能团取代的类似物显示出与吡罗昔康相同的有效抗关节炎活性，并且在炎症和伤害感受的急性试验中也具有活性。他们抑制了微摩尔浓度的环氧合酶和5-脂氧合酶的活性。化合物102（RU 43526）显示出有效的抗关节炎活性（佐剂诱发的关节炎，ED50 = 0.7 mg / kg，口服）和胃肠道耐受性（ED100大于250 mg / kg，口服），因此，目前正在接受广泛的药理评估。
• MODULATORS OF ATP-BINDING CASSETTE TRANSPORTERS
  申请人：Sheth Urvi

  公开号：US20120309758A1

  公开（公告）日：2012-12-06

  The present invention relates to modulators of ATP-Binding Cassette (“ABC”) transporters or fragments thereof, including Cystic Fibrosis Transmembrane Conductance Regulator, compositions thereof, and methods therewith. The present invention also relates to methods of treating ABC transporter mediated diseases using such modulators.

  本发明涉及调节ATP结合盒（“ABC”）转运蛋白或其片段的调节剂，包括囊性纤维化跨膜传导调节蛋白，以及相关的组合物和方法。本发明还涉及使用这些调节剂治疗ABC转运蛋白介导的疾病的方法。
• [EN] QUINOLYL AMIDE DERIVATIVES AS CCR-5 ANTAGONISTS<br/>[FR] DERIVES DE QUINOLYLE AMIDE ANTAGONISTES DE CCR-5
  申请人：SCHERING AG

  公开号：WO2004113323A1

  公开（公告）日：2004-12-29

  The present invention relates to a series of compounds which are CCR-5 receptor antagonists of the general formula (I): or a pharmaceutically acceptable salt thereof, wherein the variables are defined herein.

  本发明涉及一系列化合物，其为一般式(I)的CCR-5受体拮抗剂，或其药学上可接受的盐，其中变量在此处定义。
• Synthesis of 4-(Phenylamino)quinoline-3-carboxamides as a Novel Class of Gastric H+/K+-ATPase Inhibitors.
  作者：Minoru UCHIDA、Kenji OTSUBO、Jun MATSUBARA、Tadaaki OHTANI、Seiji MORITA、Katsuya YAMASAKI

  DOI：10.1248/cpb.43.693

  日期：——

  In search for inhibitors of gastric H+/K+-ATPase, 4-(phenylamino)quinoline-3-carboxamides were synthesized and evaluated for antisecretory activity against histamine-induced gastric acid secretion in rats. These compounds were synthesized by condensation of aniline derivatives with N-substituted 4-chloroquinoline-3-carboxamides, which were obtained from treatment of 4(1H)-quinolinone-3-carboxylic acid

  为了寻找胃H + / K + -ATP酶的抑制剂，合成了4-（苯氨基）喹啉-3-羧酰胺并评估了其对组胺诱导的大鼠胃酸分泌的抗分泌活性。这些化合物是通过将苯胺衍生物与N-取代的4-氯喹啉-3-羧酰胺缩合而合成的，后者是由亚硫酰氯处理4（1H）-喹啉酮-3-羧酸而获得的。大多数化合物抑制大鼠中组胺诱导的胃酸分泌。其中，N-烯丙基-4-（2-乙基苯基氨基）喹啉-3-羧酰胺（4h）是最有效的抑制剂，并且作为候选抗溃疡药的分布最佳。该化合物显示出可逆的K +竞争性胃H + / K + -ATPase抑制活性。