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2-溴-5-甲砜基吡啶 | 343262-51-1

中文名称
2-溴-5-甲砜基吡啶
中文别名
2-溴-5-(甲基磺酰)吡啶
英文名称
2-bromo-5-methanesulfonylpyridine
英文别名
2-bromo-5-(methylsulfonyl)pyridine;2-bromo-5-methylsulfonylpyridine
2-溴-5-甲砜基吡啶化学式
CAS
343262-51-1
化学式
C6H6BrNO2S
mdl
——
分子量
236.089
InChiKey
ZRXQHWYUAIXKRL-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:
    387.7±42.0 °C(Predicted)
  • 密度:
    1.678±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    55.4
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 危险品标志:
    Xn
  • 危险类别码:
    R22
  • 海关编码:
    2933399090
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险性描述:
    H302
  • 储存条件:
    室温且干燥

SDS

SDS:6c4a2298c0307d80dca598a4240dc311
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 2-Bromo-5-(methylsulfonyl)pyridine
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-5-(methylsulfonyl)pyridine
CAS number: 343262-51-1

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.
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: C6H6BrNO2S
Molecular weight: 236.1

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, sulfur oxides.

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
  • 下游产品
    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-5-甲砜基吡啶tris-(dibenzylideneacetone)dipalladium(0)caesium carbonate4,5-双二苯基膦-9,9-二甲基氧杂蒽三氟乙酸 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 1.0h, 生成 (R)-8-(2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethyl)-3-(5-(methylsulfonyl)pyridin-2-yl)-1-oxa-3,8-diazaspiro[4.5]decan-2-one
    参考文献:
    名称:
    [EN] INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL
    [FR] INHIBITEURS DU CANAL POTASSIQUE MÉDULLAIRE EXTERNE RÉNAL
    摘要:
    本发明提供了式I的化合物及其药学上可接受的盐,这些化合物是ROMK(Kir1.1)通道的抑制剂。这些化合物可用作利尿剂和/或钠利尿剂,并用于治疗和预防包括高血压、心力衰竭和慢性肾病在内的心血管疾病以及与过多盐分和水分潴留有关的疾病。
    公开号:
    WO2015017305A1
  • 作为产物:
    描述:
    2-溴-5-(硫代甲基)吡啶间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以95%的产率得到2-溴-5-甲砜基吡啶
    参考文献:
    名称:
    2-(3-二氟甲基-5-苯基吡唑-1-基)-5-甲磺酰吡啶(一种有效的,选择性的和口服活性的犬COX-2抑制剂)的体内和体外概况。
    摘要:
    描述了新型犬COX-2选择性抑制剂2-(3-二氟甲基-5-苯基吡唑-1-基)-5-甲磺酰吡啶的合成及其体外和体内特性。吡唑8在体外和离体全血测定中均表现出对犬COX-2的出色效价和选择性。这种新型的COX-2抑制剂在口服(po),静脉内(iv)和皮下(sc)给药后也显示出良好的药代动力学特征(pk),并且在犬滑膜炎模型中显示出出色的体内功效。
    DOI:
    10.1016/j.bmc.2004.11.048
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文献信息

  • [EN] AZOLE COMPOUNDS AS PIM INHIBITORS<br/>[FR] COMPOSÉS D'AZOLE UTILISÉS EN TANT QU'INHIBITEURS DES PIM
    申请人:AMGEN INC
    公开号:WO2012129338A1
    公开(公告)日:2012-09-27
    The invention relates to bicyclic compounds of formulas I and Ia, and salts thereof. In some embodiments, the invention relates to inhibitors or modulators of Pim-1 and/or Pim-2, and/or Pim-3 protein kinase activity or enzyme function. In still further embodiments, the invention relates to pharmaceutical compositions comprising compounds disclosed herein, and their use in the prevention and treatment of Pim kinase related conditions and diseases, preferably cancer.
    该发明涉及公式I和Ia的双环化合物及其盐。在某些实施例中,该发明涉及Pim-1和/或Pim-2和/或Pim-3蛋白激酶活性或酶功能的抑制剂或调节剂。在更进一步的实施例中,该发明涉及包含本文所披露的化合物的药物组合物,以及它们在预防和治疗Pim激酶相关疾病和病症,尤其是癌症中的用途。
  • [EN] FUSED RING COMPOUNDS AND USE THEREOF<br/>[FR] COMPOSÉS CYCLIQUES CONDENSÉS ET UTILISATION DE CEUX-CI
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2009125873A1
    公开(公告)日:2009-10-15
    The present invention aims to provide a glucokinase activator useful as a pharmaceutical agent such as an agent for the prophylaxis or treatment of diabetes, obesity and the like. The present invention provides a glucokinase activator containing a compound represented by the formula (I): wherein each symbol is defined in the specification, or a salt thereof or a prodrug thereof.
    本发明旨在提供一种葡萄糖激酶激活剂,可用作药用剂,如用于预防或治疗糖尿病、肥胖等疾病的药剂。本发明提供一种包含由式(I)表示的化合物的葡萄糖激酶激活剂:其中每个符号在规范中有定义,或其盐或前药。
  • Pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV)
    申请人:Madar J. David
    公开号:US20050215784A1
    公开(公告)日:2005-09-29
    The present invention relates to compounds that inhibit dipeptidyl peptidase IV (DPP-IV) and are useful for the prevention or treatment of diabetes, especially type II diabetes, as well as hyperglycemia, Syndrome X, hyperinsulinemia, obesity, atherosclerosis, and various immunomodulatory diseases.
    本发明涉及抑制二肽基肽酶IV(DPP-IV)的化合物,用于预防或治疗糖尿病,特别是II型糖尿病,以及高血糖、X综合征、高胰岛素血症、肥胖、动脉粥样硬化和各种免疫调节性疾病。
  • [EN] PHD INHIBITOR COMPOUNDS, COMPOSITIONS, AND USE<br/>[FR] COMPOSÉS INHIBITEURS DE PHD, COMPOSITIONS ET UTILISATION
    申请人:AKEBIA THERAPEUTICS INC
    公开号:WO2021188938A1
    公开(公告)日:2021-09-23
    The present invention provides, in part, novel small molecule inhibitors of PHD, having a structure according to Formula (A), and sub-formulas thereof: or a pharmaceutically acceptable salt thereof. The compounds provided herein can be useful for treatment of diseases including heart ( e.g. ischemic heart disease, congestive heart failure, and valvular heart disease), lung (e.g., acute lung injury, pulmonary hypertension, pulmonary fibrosis, and chronic obstructive pulmonary disease), liver (e.g. acute liver failure and liver fibrosis and cirrhosis), and kidney (e.g. acute kidney injury and chronic kidney disease) disease.
    本发明部分提供了PHD的新型小分子抑制剂,其结构符合式(A)及其亚式结构:或其药学上可接受的盐。本文提供的化合物可用于治疗包括心脏病(例如缺血性心脏病、充血性心力衰竭和瓣膜性心脏病)、肺部疾病(例如急性肺损伤、肺动脉高压、肺纤维化和慢性阻塞性肺疾病)、肝脏疾病(例如急性肝功能衰竭和肝纤维化和肝硬化)和肾脏疾病(例如急性肾损伤和慢性肾脏疾病)的疾病。
  • [EN] SUBSTITUTED CYCLOPROPYL COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF TREATMENT<br/>[FR] COMPOSÉS CYCLOPROPYLE SUBSTITUÉS, COMPOSITIONS CONTENANT DE TELS COMPOSÉS ET PROCÉDÉS DE TRAITEMENT
    申请人:MERCK SHARP & DOHME
    公开号:WO2011019538A1
    公开(公告)日:2011-02-17
    Substituted cyclopropyl compounds of the formula I: are disclosed as useful for treating or preventing type 2 diabetes and similar conditions. Pharmaceutically acceptable salts are included as well. The compounds are useful as agonists of the g-protein coupled receptor GPR-119.
    取代的环丙基化合物公式I:被披露为用于治疗或预防2型糖尿病和类似病症的有用物质。药物可接受的盐也包括在内。这些化合物作为G蛋白偶联受体GPR-119的激动剂是有用的。
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