6-溴-1-氨基异喹啉 | 215453-26-2

• 物质功能分类: 医药中间体 - 杂环化合物 - 异喹啉类化合物
• 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: 6-溴-1-氨基异喹啉
• 中文别名: 6-溴异喹啉-1-胺；6-溴异喹啉-1-基胺
• 英文名称: 6-bromoisoquinolin-1-amine
• 英文别名: 1-amino-6-bromoisoquinoline
• CAS: 215453-26-2
• 化学式: C₉H₇BrN₂
• mdl: MFCD07374395
• 分子量: 223.072
• InChiKey: PZNNAAGLKCNZKE-UHFFFAOYSA-N

物化性质

• 沸点：
  380.7±27.0 °C(Predicted)
• 密度：
  1.649±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  38.9
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2933499090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335
• 储存条件：
  2-8°C

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 6-Bromoisoquinolin-1-amine
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: 6-Bromoisoquinolin-1-amine
CAS number: 215453-26-2

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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: C9H7BrN2
Molecular weight: 223.1

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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 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

用途

6-溴-1-氨基异喹啉在药物合成中被广泛应用于抗早孕药和凝血酶抑制剂等药物。

制备

1-氨基异喹啉可通过相应的羧酸衍生物经过重排反应制得，但需要预先保护N-2位，反应完成后去除保护基团。这一过程较为繁琐且产率较低。常见的6-溴-1-氨基异喹啉的制备方法是从6-溴-1-氯异喹啉出发，依次与对甲氧基苄胺进行反应并水解得到。其合成路线如下：

反应信息

• 作为反应物：
  描述：

  6-溴-1-氨基异喹啉 在 吡啶 、 正丁基锂 作用下， 生成 N-(6-formyl-1-isoquinolinyl)benzamide
  参考文献：
  名称：

  1-Aminoisoquinoline as benzamidine isoster in the design and synthesis of orally active thrombin inhibitors

  摘要：

  Replacement of the highly basic benzamidine moiety of NAPAP by the moderately basic 1-aminoisoquinoline moiety resulted in thrombin inhibitors with improved selectivity towards trypsin and enhanced Caco-2 cell permeability. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00069-4
• 作为产物：
  描述：

  6-溴异喹啉 在 乙酸铵 、 盐酸 、 氢氧化钾 、 间氯过氧苯甲酸 、 三氯氧磷 作用下， 生成 6-溴-1-氨基异喹啉
  参考文献：
  名称：

  1-Aminoisoquinoline as benzamidine isoster in the design and synthesis of orally active thrombin inhibitors

  摘要：

  Replacement of the highly basic benzamidine moiety of NAPAP by the moderately basic 1-aminoisoquinoline moiety resulted in thrombin inhibitors with improved selectivity towards trypsin and enhanced Caco-2 cell permeability. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00069-4

文献信息

• Identification of an imidazopyridine scaffold to generate potent and selective TYK2 inhibitors that demonstrate activity in an in vivo psoriasis model
  作者：Jun Liang、Anne Van Abbema、Mercedesz Balazs、Kathy Barrett、Leo Berezhkovsky、Wade S. Blair、Christine Chang、Donnie Delarosa、Jason DeVoss、Jim Driscoll、Charles Eigenbrot、Simon Goodacre、Nico Ghilardi、Calum MacLeod、Adam Johnson、Pawan Bir Kohli、Yingjie Lai、Zhonghua Lin、Priscilla Mantik、Kapil Menghrajani、Hieu Nguyen、Ivan Peng、Amy Sambrone、Steven Shia、Jan Smith、Sue Sohn、Vickie Tsui、Mark Ultsch、Karen Williams、Lawren C. Wu、Wenqian Yang、Birong Zhang、Steven Magnuson

  DOI：10.1016/j.bmcl.2017.08.022

  日期：2017.9

  identification of an imidazopyridine class of potent and selective TYK2 inhibitors, exemplified by prototype 6, through constraint of the rotatable amide bond connecting the pyridine and aryl rings of compound 1. Further optimization led to generation of compound 30 that potently inhibits the TYK2 enzyme and the IL-23 pathway in cells, exhibits selectivity against cellular JAK2 activity, and has good pharmacokinetic

  本文我们报道咪唑并吡啶类的有效和选择性抑制剂TYK2的，由原型例举的识别6，通过可旋转的酰胺键连接的化合物的吡啶和芳基环的约束1。进一步的优化导致了化合物30的产生，该化合物有效抑制细胞中的TYK2酶和IL-23途径，表现出对细胞JAK2活性的选择性，并具有良好的药代动力学特性。在小鼠体内，化合物30PK / PD模型以及咪喹莫特诱发的牛皮癣模型中，IL-17产生的剂量依赖性降低。在这种功效模型中，IL-17的降低伴随着耳厚度的降低，表明TYK2抑制作为牛皮癣患者的治疗方法的潜力。
• [EN] SULPHONYLAMINOPYRROLIDINONE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION<br/>[FR] DÉRIVÉS SULFONYLAMINOPYRROLIDINONE, PRÉPARATION ET APPLICATION THÉRAPEUTIQUE DE CEUX-CI
  申请人：SANOFI SA

  公开号：WO2013092756A1

  公开（公告）日：2013-06-27

  The invention relates to new sulphonylaminopyrrolidinone compounds having antithrombotic activity which, in particular, inhibit blood clotting factor IXa and/ or factor Xa, to processes for their preparation and to use thereof as drugs.

  这项发明涉及具有抗血栓活性的新磺胺基吡咯烷酮化合物，特别是抑制凝血因子IXa和/或Xa，以及它们的制备方法和作为药物的用途。
• Kinase inhibitors
  申请人：——

  公开号：US20030187026A1

  公开（公告）日：2003-10-02

  Compounds having the formula 1 are useful for inhibiting protein kinases. Also disclosed are compositions which inhibit protein kinases and methods of inhibiting protein kinases in a patient.

  具有以下化学式的化合物对抑制蛋白激酶很有用。还公开了抑制蛋白激酶的组合物以及在患者中抑制蛋白激酶的方法。
• RHO-ASSOCIATED PROTEIN KINASE INHIBITOR, PHARMACEUTICAL COMPOSITION COMPRISING SAME, AND USE THEREOF
  申请人：BEIJING TIDE PHARMACEUTICAL CO., LTD.

  公开号：US20220002266A1

  公开（公告）日：2022-01-06

  A Rho-associated protein kinase (ROCK) inhibitor represented by formula (I), a pharmaceutical composition comprising same, and a use thereof for preventing or treating ROCK-mediated diseases.

  一个由公式(I)表示的Rho相关蛋白激酶(ROCK)抑制剂，包含该抑制剂的药物组合物，以及用于预防或治疗ROCK介导的疾病的应用。
• NOVEL NAPHTHYRIDINES AND ISOQUINOLINES AND THEIR USE AS CDK8/19 INHIBITORS
  申请人：Merck Patent GmbH

  公开号：US20160016951A1

  公开（公告）日：2016-01-21

  The present invention relates to naphthyridine and isoquinoline compounds, and pharmaceutically acceptable compositions thereof, useful as inhibitors of CDK8/19, and for the treatment of CDK8/19-related disorders.

  本发明涉及萘啶和异喹啉化合物，以及由此组成的药物可接受的组合物，作为CDK8/19的抑制剂，用于治疗与CDK8/19相关疾病。