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6-溴-3-碘咪唑并[1,2-a]吡嗪 | 1245644-42-1

中文名称
6-溴-3-碘咪唑并[1,2-a]吡嗪
中文别名
6-溴-3-碘咪唑并[1,2-A]吡嗪
英文名称
6-bromo-3-iodoimidazo[1,2-a]pyrazine
英文别名
——
6-溴-3-碘咪唑并[1,2-a]吡嗪化学式
CAS
1245644-42-1
化学式
C6H3BrIN3
mdl
——
分子量
323.918
InChiKey
QQRGSZAMEYFXCS-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

  • 密度:
    2.64

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    11
  • 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:
    30.2
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090
  • 危险性防范说明:
    P261,P280,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H332,H335
  • 储存条件:
    存储条件为2-8°C,避光,惰性气体环境。

SDS

SDS:86e044b18ddb9a73cfce722037666ad2
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 6-Bromo-3-iodoimidazo[1,2-a]pyrazine
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 6-Bromo-3-iodoimidazo[1,2-a]pyrazine
CAS number: 1245644-42-1

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, refrigerated.
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: C6H3BrIN3
Molecular weight: 323.9

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, hydrogen Iodide.

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:
    6-溴-3-碘咪唑并[1,2-a]吡嗪N-甲基吗啉(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloridepotassium phosphate四(三苯基膦)钯potassium carbonate三氟乙酸 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 55.0h, 生成 4-(6-(4-(4-amino-4-methylpiperidine-1-carbonyl)-3-fluorophenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile
    参考文献:
    名称:
    BICYCLIC HETEROCYCLIC DERIVATIVES AS MNK1 AND MNK2 MODULATORS AND USES THEREOF
    摘要:
    本发明涉及某些化合物(例如咪唑吡嗪、咪唑吡啶、咪唑吡嗪和咪唑嘧啶化合物),这些化合物作为MAP激酶相互作用激酶MNK2a、MNK2b、MNK1a和MNK1b的抑制剂。本发明还涉及包含这些化合物的药物组合物,以及利用这些化合物制备用于预防和治疗疾病(例如增生性疾病(例如癌症)、炎症性疾病、阿尔茨海默病)的药物的用途,以及治疗这些疾病的方法。
    公开号:
    US20140371199A1
  • 作为产物:
    描述:
    2-溴吡嗪[4,5-a]并吡咯N-碘代丁二酰亚胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 10.0h, 以530 mg的产率得到6-溴-3-碘咪唑并[1,2-a]吡嗪
    参考文献:
    名称:
    [EN] SUBSTITUTED BENZOFURAN COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES
    [FR] COMPOSÉS BENZOFURANES SUBSTITUÉS ET LEURS PROCÉDÉS D'UTILISATION POUR LE TRAITEMENT DE MALADIES VIRALES
    摘要:
    本发明涉及一种具有式(I)的化合物,该化合物可用作丙型肝炎病毒(HCV)NS5B聚合酶抑制剂,以及该类化合物的合成,以及利用该类化合物抑制HCV NS5B聚合酶活性,用于治疗或预防HCV感染,以及在基于细胞的系统中抑制HCV病毒复制和/或病毒产生。
    公开号:
    WO2013034048A1
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文献信息

  • HETEROARYL CARBOXAMIDE COMPOUNDS AS INHIBITORS OF RIPK2
    申请人:Boehringer Ingelheim International GmbH
    公开号:US20180072717A1
    公开(公告)日:2018-03-15
    The present invention relates to compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , X, Y, and HET are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes
    本发明涉及以下式(I)的化合物: 或其药学上可接受的盐,其中R 1 ,R 2 ,X,Y和HET如本文所定义。该发明还涉及包含这些化合物的药物组合物,使用这些化合物治疗各种疾病和紊乱的方法,制备这些化合物的过程以及在这些过程中有用的中间体。
  • [EN] BICYCLIC HETEROCYCLIC DERIVATIVES AS MNK1 AND MNK2 MODULATORS AND USES THEREOF<br/>[FR] DÉRIVÉS HÉTÉROCYCLIQUES BICYCLIQUES À TITRE DE MODULATEURS DE MNK1 ET MNK2 ET LEURS UTILISATIONS
    申请人:AGENCY SCIENCE TECH & RES
    公开号:WO2013147711A1
    公开(公告)日:2013-10-03
    The present invention relates to certain compounds (e.g., imidazopyrazine, imidazopyridine, imidazopyridazine and imidazpyrimidine compounds) that act as inhibitors of the MAP kinase interacting kinases MNK2a, MNK2b, MNK1a, and MNK1b. The present invention further relates to pharmaceutical compositions comprising these compounds, and to the use of the compounds for the preparation of a medicament for the prophylaxis and treatment of diseases (e.g., proliferative diseases (e.g., cancer), inflammatory diseases, Alzheimer's disease), as well as methods of treating these diseases.
    本发明涉及某些化合物(例如咪唑吡嗪、咪唑吡啶、咪唑吡嗪和咪唑嘧啶化合物),这些化合物作为MAP激酶相互作用激酶MNK2a、MNK2b、MNK1a和MNK1b的抑制剂。本发明还涉及包含这些化合物的药物组合物,以及利用这些化合物制备用于预防和治疗疾病(例如增生性疾病(例如癌症)、炎症性疾病、阿尔茨海默病)的药物的用途,以及治疗这些疾病的方法。
  • Nitrogen bicyclic compounds as inhibitors for Scyl1 and Grk5
    申请人:Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V.
    公开号:EP2818471A1
    公开(公告)日:2014-12-31
    The present invention relates to compounds assumed to be capable of modulating the activity of the proteins ScyI1 and Grk5, thereby regulating the expression and/or release of insulin as well as to pharmaceutical compositions containing such compounds and the use thereof especially for the treatment of a metabolic disease such as diabetes, obesity and impaired adipogenesis.
    本发明涉及假设能够调节蛋白质ScyI1和Grk5活性的化合物,从而调节胰岛素的表达和/或释放,以及包含此类化合物的药物组合物及其用途,特别是用于治疗糖尿病、肥胖和脂肪生成受损等代谢性疾病。
  • BICYCLIC HETEROARYL DERIVATIVES AS MNK1 AND MNK2 MODULATORS AND USES THEREOF
    申请人:Agency for Science, Technology and Research
    公开号:US20150038506A1
    公开(公告)日:2015-02-05
    The present invention relates to certain compounds (e.g., imidazopyrazine, imidazopyridine, imidazopyridazine and imidazpyrimidine compounds) that act as inhibitors of the MAP kinase interacting kinases MNK2a, MNK2b, MNK1a, and MNK1b. The present invention further relates to pharmaceutical compositions comprising these compounds, and to the use of the compounds for the preparation of a medicament for the prophylaxis and treatment of diseases (e.g., proliferative diseases (e.g., cancer), neurodegenerative diseases (e.g., Alzheimer's disease), metabolic diseases (e.g. diabetes), neurodevelopmental disorders (e.g. autism), or psychiatric disorders (e.g. schizophrenia or anxiety)) as well as methods of treating these diseases.
    本发明涉及某些化合物(例如,咪唑吡嗪、咪唑吡啶、咪唑吡嗪和咪唑嘧啶化合物),它们作为MAP激酶相互作用激酶MNK2a、MNK2b、MNK1a和MNK1b的抑制剂。本发明还涉及包含这些化合物的药物组合物,以及使用这些化合物制备预防和治疗疾病(例如增生性疾病(例如癌症),神经退行性疾病(例如阿尔茨海默病),代谢性疾病(例如糖尿病),神经发育障碍(例如自闭症),或精神障碍(例如精神分裂症或焦虑症))的药物以及治疗这些疾病的方法。
  • SUBSTITUED BENZOFURAN COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES
    申请人:McComas Casey C.
    公开号:US20150246902A1
    公开(公告)日:2015-09-03
    The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.
    本发明涉及式(I)的化合物,这些化合物可用作丙型肝炎病毒(HCV)NS5B聚合酶抑制剂,以及这些化合物的合成,以及使用这些化合物来抑制HCV NS5B聚合酶活性,治疗或预防HCV感染,并在细胞系统中抑制HCV病毒复制和/或病毒产生。
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