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2-溴-4-甲基-5-氨基吡啶 | 156118-16-0

中文名称
2-溴-4-甲基-5-氨基吡啶
中文别名
2-溴-5-氨基-4-甲基吡啶;6-溴-4-甲基-3-氨基吡啶;3-氨基-6-溴-4-甲基吡啶
英文名称
6-bromo-4-methylpyridin-3-amine
英文别名
6-bromo-4-methylpyridin-3-ylamine;5-amino-2-bromo-4-methylpyridine
2-溴-4-甲基-5-氨基吡啶化学式
CAS
156118-16-0
化学式
C6H7BrN2
mdl
MFCD08277280
分子量
187.039
InChiKey
MVDBPMJQCXZKRB-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    306.9±37.0 °C(Predicted)
  • 密度:
    1.593±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    38.9
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 危险等级:
    6.1
  • 海关编码:
    2933399090
  • 危险品运输编号:
    UN 2811
  • 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

SDS:54a77bfe0aa51f6133080d739db35d6a
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Bromo-4-methyl-5-aminopyridine
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 2-Bromo-4-methyl-5-aminopyridine
CAS number: 156118-16-0

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.

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.

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.

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:

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.

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: C6H7BrN2
Molecular weight: 187

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.

Section 11. Toxicological information
No data.

Section 12. Ecological information
No data.

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.

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

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.


SECTION 16 - ADDITIONAL INFORMATION
N/A

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-溴-4-甲基-5-氨基吡啶硫酸 、 sodium nitrite 作用下, 以 为溶剂, 反应 24.5h, 以52%的产率得到6-溴-4-甲基-3-羟基吡啶
    参考文献:
    名称:
    [EN] PYRROLO[2,3-C]PYRIDINES AS IMAGING AGENTS FOR NEUROFIBRILARY TANGLES
    [FR] PYRROLO [2,3-C] PYRIDINES EN TANT QU'AGENTS D'IMAGERIE D'ENCHEVÊTREMENTS NEUROFIBRILLAIRES
    摘要:
    公开了式(I)的吡咯吡啶化合物或其药学上可接受的盐,这些化合物可能适用于成像tau聚集体、β-折叠聚集体、β-淀粉样聚集体或α-突触核蛋白聚集体,因此在结合和成像阿尔茨海默病患者的tau聚集体方面是有用的。更具体地,这些化合物被用作正电子发射断层扫描(PET)成像中的示踪剂,用于研究体内脑部的tau沉积,以便诊断阿尔茨海默病和其他以tau病理为特征的神经退行性疾病。此外,这些化合物对于测量治疗阿尔茨海默病和其他以tau病理为特征的神经退行性疾病的临床疗效是有用的。
    公开号:
    WO2015188368A1
  • 作为产物:
    参考文献:
    名称:
    通过构象约束发现(1H-吡唑并[3,4-c]吡啶-5-基)磺酰胺类似物作为乙型肝炎病毒衣壳装配调节剂。
    摘要:
    在临床前和临床研究中,均已建议乙型肝炎病毒(HBV)衣壳装配调节剂(CAMs)是有效的抗HBV药物。除了阻断HBV复制外,CAM还可以减少共价闭合环状DNA(cccDNA)的形成,这说明了HBV感染的持续性。在这里,我们通过限制氨基磺酰基苯甲酰胺衍生物的构象,描述了作为新的CAM化学型的(1 H-吲唑-5-基)磺酰胺和(1 H-吡唑并[3,4- c ]吡啶-5-基)磺酰胺的发现。 。铅优化导致化合物56的EC 50值为0.034μM,在小鼠肝微粒体中具有良好的代谢稳定性。为了增加溶解度,氨基酸前药(制备65)及其柠檬酸盐(67)。在基于水动力注射的HBV感染小鼠模型中,化合物67剂量依赖性地抑制HBV复制,而56则由于其次优溶解性而未显示体内抗HBV活性。这类化合物可作为开发新型抗HBV药物的起点。
    DOI:
    10.1021/acs.jmedchem.0c00292
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文献信息

  • [EN] NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF INFLAMMATORY DISORDERS<br/>[FR] NOUVEAUX COMPOSÉS ET COMPOSITIONS PHARMACEUTIQUES LES COMPRENANT POUR LE TRAITEMENT DE TROUBLES INFLAMMATOIRES
    申请人:GALAPAGOS NV
    公开号:WO2017012647A1
    公开(公告)日:2017-01-26
    The present invention discloses compounds according to Formula (I), wherein R1, R3, R4, R5, L1, and Cy are as defined herein. The present invention also provides compounds, methods for the production of said compounds of the invention, pharmaceutical compositions comprising the same and their use in allergic or inflammatory conditions, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IL6 and/or interferons. The present invention also methods for the prevention and/or treatment of the aforementioned diseases by administering a compound of the invention.
    本发明公开了根据式(I)的化合物,其中R1、R3、R4、R5、L1和Cy如本文所定义。本发明还提供了该发明的化合物、制备该化合物的方法、包括相同化合物的药物组合物以及它们在过敏或炎症症状、自身免疫疾病、增殖性疾病、移植排斥、涉及软骨周转障碍的疾病、先天软骨畸形和/或与IL6和/或干扰素过度分泌相关的疾病中的使用。本发明还提供了通过给予该发明的化合物来预防和/或治疗上述疾病的方法。
  • [EN] SUBSTITUTED PYRIDINE COMPOUNDS AS CRAC MODULATORS<br/>[FR] COMPOSÉS SUBSTITUÉS DE PYRIDINE EN TANT QUE MODULATEURS DE CRAC
    申请人:LUPIN LTD
    公开号:WO2013164769A1
    公开(公告)日:2013-11-07
    The present invention relates to compounds described herein Formula (I) and pharmaceutical acceptable salts thereof, which modulate the activity of calcium release- activated calcium (CRAC) channel. The invention also describes the compounds of Formula (I)and pharmaceutical compositions containing such compounds thereof for treating, managing, and/or lessening the severity of diseases, disorders, syndromes or conditions associated with the modulation of calcium release-activated calcium (CRAC) channel.
    本发明涉及式(I)描述的化合物以及其中医药可接受的盐,这些化合物能够调节钙释放激活钙(CRAC)通道的活性。该发明还描述了式(I)的化合物以及包含这些化合物的药物组合物,用于治疗、管理和/或减轻与调节钙释放激活钙(CRAC)通道相关联的疾病、障碍、综合征或状况的严重性。
  • [EN] INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE<br/>[FR] INHIBITEURS DE TYROSINE KINASE DE BRUTON ET LEURS PROCÉDÉS D'UTILISATION
    申请人:JANSSEN PHARMACEUTICA NV
    公开号:WO2018103058A1
    公开(公告)日:2018-06-14
    Compounds of formula (I') and methods of their use and preparation, as well as compositions comprising compounds of formula (I').
    公式(I')的化合物及其使用和制备方法,以及包含公式(I')化合物的组合物。
  • [EN] 3-(1H-PYRROLO[3,2-C]PYRIDIN-2-YL)-1H-PYRAZOLO[3,4-C]PYRIDINES AND THERAPEUTIC USES THEREOF<br/>[FR] 3-(1H-PYRROLO[3,2-C]PYRIDIN-2-YL)-1H-PYRAZOLO[3,4-C]PYRIDINES ET LEURS UTILISATIONS THÉRAPEUTIQUES
    申请人:SAMUMED LLC
    公开号:WO2017023984A1
    公开(公告)日:2017-02-09
    6-Azaindazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of a 6-azaindazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, fibrotic disorders, bone or cartilage diseases, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases and neurological conditions/disorders/diseases due to mutations or dysregulation of the Wnt pathway and/or of one or more of Wnt signaling components. Also provided are methods for treating Wnt-related disease states.
    披露了用于治疗各种疾病和病理的6-氮杂吲唑化合物。更具体地,本公开涉及使用6-氮杂吲唑化合物或其类似物,治疗通过Wnt途径信号激活所特征化的疾病(例如癌症、异常细胞增殖、血管生成、纤维化疾病、骨骼或软骨疾病和骨关节炎),调节由Wnt途径信号介导的细胞事件,以及由于Wnt途径和/或一个或多个Wnt信号组分的突变或失调而导致的遗传疾病和神经病理状况/障碍/疾病。还提供了治疗与Wnt相关疾病状态的方法。
  • [EN] NOVEL COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF FOR THE TREATMENT OF INFLAMMATORY DISORDERS<br/>[FR] NOUVEAUX COMPOSÉS ET COMPOSITIONS PHARMACEUTIQUES ASSOCIÉES POUR LE TRAITEMENT DE TROUBLES INFLAMMATOIRES
    申请人:GALAPAGOS NV
    公开号:WO2019076716A1
    公开(公告)日:2019-04-25
    The present invention discloses compounds according to Formula I: (Formula I) Wherein R1, L1, R2, L2, R3, Cy, and the subscript n are as defined herein. The present invention relates to compounds, methods for their production, pharmaceutical compositions comprising the same, and methods of treatment using the same, for the prophylaxis and/or treatment of allergic diseases, inflammatory diseases, metabolic diseases, autoinflammatory diseases, autoimmune diseases, proliferative diseases, transplantation rejection, diseases involving impairment of cartilage turnover, congenital cartilage malformations, and/or diseases associated with hypersecretion of IFNα, IL12 and/or IL23 by administering the compound of the invention.
    本发明公开了根据式I的化合物:(式I)其中R1,L1,R2,L2,R3,Cy和下标n如本文所定义。本发明涉及化合物、其生产方法、包括其在内的药物组合物,以及使用这些化合物进行预防和/或治疗过敏性疾病、炎症性疾病、代谢性疾病、自身炎症性疾病、自身免疫性疾病、增殖性疾病、移植排斥、涉及软骨周转受损、先天软骨畸形和/或与IFNα、IL12和/或IL23过度分泌相关的疾病的治疗方法。
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