5-溴-2-(三氟甲氧基)苯甲腈 | 1210906-15-2

• 物质功能分类: 有机原料 - 有机氟化合物 - 氟苯腈系列
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 中文名称: 5-溴-2-(三氟甲氧基)苯甲腈
• 中文别名: 2-三氟甲氧基-5-溴苯腈；5-溴-2-(三氟甲氧基)苯腈
• 英文名称: 5-bromo-2-(trifluoromethoxy)benzonitrile
• CAS: 1210906-15-2
• 化学式: C₈H₃BrF₃NO
• 分子量: 266.017
• InChiKey: XYVAUHKIIHYPAX-UHFFFAOYSA-N

物化性质

• 沸点：
  244℃
• 密度：
  1.75
• 闪点：
  101℃

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  33
• 氢给体数：
  0
• 氢受体数：
  5

安全信息

• 海关编码：
  2926909090
• 危险性防范说明：
  P280,P305+P351+P338
• 危险性描述：
  H302

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 5-Bromo-2-(trifluoromethoxy)benzonitrile
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: 5-Bromo-2-(trifluoromethoxy)benzonitrile
CAS number: 1210906-15-2

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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: C8H3BrF3NO
Molecular weight: 266

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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, hydrogen bromide.

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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

制备方法与用途

应用：2-三氟甲氧基-5-溴苯腈可用作有机合成中间体和医药中间体，在实验室研发过程中及医药化工合成中发挥重要作用。

反应信息

• 作为反应物：
  描述：

  5-溴-2-(三氟甲氧基)苯甲腈 在 tris-(dibenzylideneacetone)dipalladium(0) 、 1,3-二氯-5,5-二甲基海因 、 溶剂黄146 、 N,N-二异丙基乙胺 、 4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下， 以 1,4-二氧六环 、 水 、 乙腈 为溶剂， 反应 23.0h， 生成 3-cyano-N-[1-(3,4-dichlorophenyl)-2-(dimethylamino)ethyl]-4-(trifluoromethoxy)benzenesulfonamide
  参考文献：
  名称：

  [EN] MODULATORS OF PROTEIN PHOSPHATASE 2A (PP2A) AND METHODS USING SAME
  [FR] MODULATEURS DE LA PROTÉINE PHOSPHATASE 2A (PP2A) ET LEURS PROCÉDÉS D'UTILISATION

  摘要：

  本公开涉及部分与蛋白磷酸酶2A（PP2A）的化学调节剂有关，包括式（I）的化合物。本公开的化合物在治疗、预防和/或改善癌症、糖尿病、自身免疫疾病、固体器官移植排斥、移植物抗宿主病、慢性阻塞性肺疾病（COPD）、非酒精性脂肪性肝病、腹主动脉瘤、慢性肝病、心力衰竭、神经退行性疾病和心肌肥厚方面具有用处。

  公开号：

  WO2022167866A1
• 作为产物：
  描述：

  5-溴-2-三氟甲氧基苯甲醛 在 盐酸羟胺 、 1-丙基磷酸酐 、 三乙胺 作用下， 以 乙酸乙酯 为溶剂， 反应 8.0h， 以86%的产率得到5-溴-2-(三氟甲氧基)苯甲腈
  参考文献：
  名称：

  ピペリジニルピラゾロピリジン誘導体の結晶

  摘要：

  具有LECITHIN CHOLESTEROL ACYLTRANSFERASE（LCAT）活化作用的化合物，用作动脉硬化症、动脉硬化性心脏病、冠状动脉性心脏病（心力衰竭、心肌梗塞、心绞痛、心脏缺血、心血管障碍和血管形成性再狭窄等）、脑血管疾病（中风和脑梗塞等）、外周血管疾病（糖尿病血管并发症等）、脂质异常症、低HDL胆固醇血症、或肾脏疾病的治疗剂或预防剂，特别是作为抗动脉硬化剂的有效成分的有用化合物的提供。 解决方案：由通式（I）表示的化合物或其药理上可接受的盐的晶体。【其中，R可以是可取代的芳基，或者是可取代的杂环芳基。】【图像未包含】

  公开号：

  JP2015113323A

文献信息

• [EN] PYRROLIDINE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, AND THEIR USE IN THERAPY<br/>[FR] DÉRIVÉS DE PYRROLIDINE, COMPOSITIONS PHARMACEUTIQUES LES CONTENANT, ET LEUR UTILISATION EN THÉRAPIE
  申请人：ABBVIE DEUTSCHLAND

  公开号：WO2014140310A1

  公开（公告）日：2014-09-18

  The present invention relates to pyrrolidine derivatives of formula (I), or a physiologically tolerated salt thereof. The invention relates to pharmaceutical compositions comprising such pyrrolidine derivatives, and the use of such pyrrolidine derivatives for therapeutic purposes. The pyrrolidine derivatives are GlyT1 inhibitors.

  本发明涉及式(I)的吡咯烷衍生物，或其生理耐受盐。该发明涉及包含此类吡咯烷衍生物的药物组合物，以及利用此类吡咯烷衍生物进行治疗的用途。这些吡咯烷衍生物是GlyT1抑制剂。
• ピペリジニルピラゾロピリジン誘導体の結晶
  申请人：第一三共株式会社

  公开号：JP2015113323A

  公开（公告）日：2015-06-22

  【課題】レシチンコレステロールアセチルトランスフェラーゼ（ＬＣＡＴ）活性化作用を有し、動脈硬化症、動脈硬化性心疾患、冠状動脈性心疾患（心不全、心筋梗塞、狭心症、心虚血、心血管障害及び血管形成性再狭窄を含む）、脳血管疾患（脳卒中及び脳梗塞を含む）、末梢血管疾患（糖尿病血管合併症を含む）、脂質異常症、低ＨＤＬコレステロール血症、若しくは、腎疾患の治療剤又は予防剤、特に、抗動脈硬化剤の有効成分として有用な化合物の提供。【解決手段】一般式（Ｉ）で表される化合物、又はその薬理上許容される塩の結晶。[Ｒは、置換されてよいアリール基、又は、置換されてよいヘテロアリール基。］【選択図】なし

  具有LECITHIN CHOLESTEROL ACYLTRANSFERASE（LCAT）活化作用的化合物，用作动脉硬化症、动脉硬化性心脏病、冠状动脉性心脏病（心力衰竭、心肌梗塞、心绞痛、心脏缺血、心血管障碍和血管形成性再狭窄等）、脑血管疾病（中风和脑梗塞等）、外周血管疾病（糖尿病血管并发症等）、脂质异常症、低HDL胆固醇血症、或肾脏疾病的治疗剂或预防剂，特别是作为抗动脉硬化剂的有效成分的有用化合物的提供。 解决方案：由通式（I）表示的化合物或其药理上可接受的盐的晶体。【其中，R可以是可取代的芳基，或者是可取代的杂环芳基。】【图像未包含】
• Tetrahydroimidazo(1,5-D)[1,4]Oxazepine Derivative
  申请人：Eisai R&D Management Co., Ltd.

  公开号：US20140243316A1

  公开（公告）日：2014-08-28

  A compound represented by the following formula (I) or a pharmaceutically acceptable salt thereof works as an mGluR2 antagonist, and is applicable as a therapeutic agent for neurological disorders related to glutamate dysfunction and diseases involving the mGluR2, such as Alzheimer's disease: wherein R is a hydrogen atom, a C 1-6 alkyl group or the like, R 1 is a C 1-6 alkyl group, a C 1-6 alkoxy group or the like, R 2 is a halogen atom, a C 1-6 alkyl group, a C 1-6 alkoxy group or the like, R 3 is a hydrogen atom, a C 1-6 alkyl group or the like, and R 4 is a C 1-6 alkyl group or the like.

  以下公式（I）表示的化合物或其药用可接受盐作为mGluR2拮抗剂，可用作治疗与谷氨酸功能障碍相关的神经疾病和涉及mGluR2的疾病，如阿尔茨海默病：其中R是氢原子、C1-6烷基或类似物，R1是C1-6烷基、C1-6甲氧基或类似物，R2是卤素原子、C1-6烷基、C1-6甲氧基或类似物，R3是氢原子、C1-6烷基或类似物，R4是C1-6烷基或类似物。
• [EN] N-[2-(1 -BENZYLPIPERIDIN-4-YL)ETHYL]-4-(PYRAZIN-2-YL)-PIPERAZINE-1 -CARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS MUSCARINIC RECEPTOR 4 (M4) ANTAGONISTS FOR TREATING NEUROLOGICAL DISEASES<br/>[FR] DÉRIVÉS DE N-[2-(1-BENZYLPIPÉRIDIN-4-YL)ÉTHYL]-4-(PYRAZIN-2-YL)-PIPÉRAZINE-1-CARBOXAMIDE ET COMPOSÉS APPARENTÉS EN TANT QU'ANTAGONISTES DU RÉCEPTEUR MUSCARINIQUE 4 (M4) POUR LE TRAITEMENT DE MALADIES NEUROLOGIQUES
  申请人：NEUROCRINE BIOSCIENCES INC

  公开号：WO2017079641A1

  公开（公告）日：2017-05-11

  Provided herein are small molecule compounds of the following formula (I): or a stereoisomer, tautomer, solvate, ester or pharmaceutically acceptable salt thereof, wherein A, B, C, Li, L 2, Ri, R 2, R 3, R 4, R 5, w, x, y and z are as defined herein. Methods for treating diseases/ disorders by antagonizing muscarinic receptors, including specifically antagonizing muscarinic receptor 4 (M4), are also disclosed. Such diseases/disorders are e.g. neurological diseases/disorders such as e.g. Alzheimer's Disease, Lewy Body Dementia and the cognitive deficits associated with schizophrenia, Parkinson's Disease, drug induced Parkinsonism, dyskinesias, dystonia, chorea, levodopa induced dyskinesia, cerebral palsy, progressive supranuclear palsy, and Huntington's disease. Preferred compounds are e.g. N-[2-(l-benzylpiperidin-4-yl)ethyl]-4- (pyrazin-2-yl)-piperazine-1-carboxamide derivatives and related compounds wherein the pyrazine has been replaced by e.g. pyridazine, pyrimidine, pyridine or phenyl.

  本文提供了以下化学式（I）的小分子化合物，或其立体异构体、互变异构体、溶剂化合物、酯或药用可接受的盐，其中A、B、C、Li、L 2、Ri、R 2、R 3、R 4、R 5、w、x、y和z的定义如本文所述。还公开了通过拮抗毒蕈碱受体来治疗疾病/障碍的方法，包括特别是拮抗毒蕈碱受体4（M4）。这些疾病/障碍包括神经系统疾病/障碍，如阿尔茨海默病、路易体痴呆症以及与精神分裂症、帕金森病、药物引起的帕金森综合症、运动障碍、肌张力障碍、舞蹈症、左多巴诱发的运动障碍、脑瘫、进行性核上性麻痹和亨廷顿病相关的认知缺陷等。首选化合物是例如N-[2-(1-苄基哌啶-4-基)乙基]-4-(吡嗪-2-基)-哌嗪-1-甲酰胺衍生物和相关化合物，其中吡嗪已被取代为例如吡啶、嘧啶、吡啶或苯基。
• Piperidinylpyrazolopyridine derivative
  申请人：Daiichi Sankyo Company, Limited

  公开号：US09150575B2

  公开（公告）日：2015-10-06

  A compound represented by the general formula (I) or a pharmacologically acceptable salt thereof has an excellent LCAT-activating effect and is useful as an active ingredient in a therapeutic or prophylactic agent for arteriosclerosis, arteriosclerotic heart disease, coronary heart disease (including heart failure, myocardial infarction, angina pectoris, cardiac ischemia, cardiovascular disturbance, and restenosis caused by angiogenesis), cerebrovascular disease (including stroke and cerebral infarction), peripheral vascular disease (including diabetic vascular complications), dyslipidemia, hypo-HDL-cholesterolemia, or renal disease, particularly, an anti-arteriosclerotic agent, wherein R is an optionally substituted aryl group or an optionally substituted heteroaryl group.

  化合物的一般式为（I），或其药理学上可接受的盐，具有出色的LCAT激活作用，可用作治疗或预防动脉硬化、动脉硬化性心脏病、冠心病（包括心力衰竭、心肌梗塞、心绞痛、心肌缺血、心血管紊乱和由血管生成引起的再狭窄）、脑血管疾病（包括中风和脑梗塞）、周围血管疾病（包括糖尿病血管并发症）、血脂异常、低HDL胆固醇血症或肾脏疾病的治疗或预防剂的活性成分，特别是抗动脉硬化剂，其中R是可选取代的芳基或可选取代的杂环基。