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5-溴-N-(2-甲氧基乙基)嘧啶-2-胺 | 886365-79-3

中文名称
5-溴-N-(2-甲氧基乙基)嘧啶-2-胺
中文别名
(5-溴-2-嘧啶)-(2-甲氧基乙基)-胺
英文名称
5-bromo-N-(2-methoxyethyl)pyrimidin-2-amine
英文别名
5-Bromo-2-(2-methoxyethylamino)pyrimidine
5-溴-N-(2-甲氧基乙基)嘧啶-2-胺化学式
CAS
886365-79-3
化学式
C7H10BrN3O
mdl
——
分子量
232.08
InChiKey
HIDHZHFCKYPDIW-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    12
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    47
  • 氢给体数:
    1
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933599090
  • 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:
    应存放在室温、避光且充满惰性气体的环境中。

SDS

SDS:d01c79116f86ecb44ae422b50ac9a2c2
查看
Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 5-Bromo-(2-methoxyethylamino)pyrimidine
Synonyms: 5-Bromo-N-(2-methoxyethyl)pyrimidin-2-amine

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

Section 3. Composition/information on ingredients.
Ingredient name: 5-Bromo-(2-methoxyethylamino)pyrimidine
CAS number: 886365-79-3

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: C7H10BrN3O
Molecular weight: 232.1

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.

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

反应信息

  • 作为反应物:
    描述:
    5-溴-N-(2-甲氧基乙基)嘧啶-2-胺potassium phosphate1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 XPhos Pd G2 、 potassium acetate 作用下, 以 1,4-二氧六环 为溶剂, 反应 4.5h, 生成 (6-{2-[(2-methoxyethyl)amino]pyrimidin-5-yl}-2-pyridyl)methyl N-carbamimidoylcarbamate
    参考文献:
    名称:
    [EN] PYRIDINYL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF AS AOC3 INHIBITORS
    [FR] DÉRIVÉS DE PYRIDINYLE, COMPOSITIONS PHARMACEUTIQUES ET UTILISATIONS DE CEUX-CI EN TANT QU'INHIBITEURS D'AOC3
    摘要:
    该发明涉及公式(I)中的新吡啶基衍生物,其中R1和A如描述和索赔中所定义,其用作药物,用于其治疗用途的方法以及含有它们的药物组合物。
    公开号:
    WO2017194453A1
  • 作为产物:
    描述:
    5-溴-2-氯嘧啶2-甲氧基乙胺potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 6.0h, 以92.3%的产率得到5-溴-N-(2-甲氧基乙基)嘧啶-2-胺
    参考文献:
    名称:
    [EN] HETEROARYL COMPOUNDS AND PHARMACEUTICAL APPLICATIONS THEREOF
    [FR] COMPOSÉS HÉTÉROARYLES ET LEURS APPLICATIONS PHARMACEUTIQUES
    摘要:
    本发明提供的是一种杂环芳基化合物或其立体异构体、几何异构体、互变异构体、消旋体、N-氧化物、水合物、溶剂合物、代谢物、药学上可接受的盐或其前药,以及含有本文所披露的化合物的药物组合物。本发明还提供的是使用本文所披露的化合物或其药物组合物制造用于治疗自身免疫疾病或增殖性疾病的药物。
    公开号:
    WO2016000615A1
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文献信息

  • [EN] BIARYLAMIDE INHIBITORS OF LEUKOTRIENE PRODUCTION<br/>[FR] INHIBITEURS BIARYLAMIDE DE PRODUCTION DE LEUKOTRIÈNES
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2012082817A1
    公开(公告)日:2012-06-21
    The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, wherein A, B, C, R1a, R1b, R2, R3, R4a and R4b 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.
    本发明涉及式(I)的化合物及其药学上可接受的盐,其中A、B、C、R1a、R1b、R2、R3、R4a和R4b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疾病的方法,制备这些化合物的方法以及在这些过程中有用的中间体。
  • [EN] BIARYL COMPOUNDS AND METHODS OF USE THEREOF<br/>[FR] COMPOSÉS BIARYLES ET PROCÉDÉS D'UTILISATION DE CEUX-CI
    申请人:AMBIT BIOSCIENCES CORP
    公开号:WO2011022473A1
    公开(公告)日:2011-02-24
    Provided herein are compounds for treatment of KIT, CSF-1R and/or FLT3 kinase mediated diseases. Also provided are pharmaceutical compositions comprising the compounds and methods of using the compounds and compositions.
    本文提供了用于治疗KIT、CSF-1R和/或FLT3激酶介导疾病的化合物。还提供了包含这些化合物的药物组合物以及使用这些化合物和组合物的方法。
  • [EN] INDAZOLE DERIVATIVES<br/>[FR] DÉRIVÉS D'INDAZOLE
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2013130855A1
    公开(公告)日:2013-09-06
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, and R6 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, to pharmaceutical compositions which contain them, and to their use for treating obesity and related diseases, disorders, and conditions associated with MetAP2.
    公开了Formula 1的化合物及其药用盐,其中R1、R2、R3、R4、R5和R6在规范中有定义。本公开还涉及制备Formula 1化合物的材料和方法,含有这些化合物的药物组合物,以及它们用于治疗肥胖和与MetAP2相关的疾病、紊乱和症状的用途。
  • COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR
    申请人:Ibrahim Prabha N.
    公开号:US20110183988A1
    公开(公告)日:2011-07-28
    Compounds and salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof and uses thereof are described. In certain aspects and embodiments, the described compounds or salts thereof, formulations thereof, conjugates thereof, derivatives thereof, forms thereof are active on each of B-Raf, B-Raf V600E and c-Raf-1 protein kinase. In certain aspects and embodiments, the described compounds are active in inhibiting proliferation of a Ras mutant cell line. Also described are methods of use thereof to treat diseases and conditions, including melanoma, glioma, glioblastoma, pilocytic astrocytoma, liver cancer, biliary tract cancer, cholangiocarcinoma, colorectal cancer, lung cancer, bladder cancer, gallbladder cancer, breast cancer, pancreatic cancer, thyroid cancer, kidney cancer, ovarian cancer, adrenocortical cancer, prostate cancer, gastrointestinal stromal tumors, medullary thyroid cancer, tumor angiogenesis, acute myeloid leukemia, chronic myelomonocytic leukemia, childhood acute lymphoblastic leukemia, plasma cell leukemia, and multiple myeloma.
    描述了化合物及其盐、制剂、共轭物、衍生物、形式和用途。在某些方面和实施例中,所述的化合物或其盐、制剂、共轭物、衍生物、形式对B-Raf、B-Raf V600E和c-Raf-1蛋白激酶均具有活性。在某些方面和实施例中,所述的化合物在抑制Ras突变细胞系增殖方面具有活性。还描述了使用它们治疗疾病和病况的方法,包括黑色素瘤、胶质瘤、胶质母细胞瘤、毛细胞星形细胞瘤、肝癌、胆管癌、胆管细胞癌、结直肠癌、肺癌、膀胱癌、胆囊癌、乳腺癌、胰腺癌、甲状腺癌、肾癌、卵巢癌、肾上腺皮质癌、前列腺癌、胃肠道间质瘤、髓样甲状腺癌、肿瘤血管生成、急性髓系白血病、慢性髓细胞/单核细胞白血病、儿童急性淋巴细胞白血病、浆细胞白血病和多发性骨髓瘤。
  • BIARYL COMPOUNDS AND METHODS OF USE THEREOF
    申请人:Abraham Sunny
    公开号:US20130035326A1
    公开(公告)日:2013-02-07
    Provided herein are compounds for treatment of KIT, CSF-1R and/or FLT3 kinase mediated diseases. Also provided are pharmaceutical compositions comprising the compounds and methods of using the compounds and compositions.
    本文提供了用于治疗KIT、CSF-1R和/或FLT3激酶介导的疾病的化合物。还提供了包含这些化合物的制药组合物以及使用这些化合物和组合物的方法。
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