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3-氨基-5-甲氧基吡啶 | 64436-92-6

中文名称
3-氨基-5-甲氧基吡啶
中文别名
5-甲氧基-吡啶-3-基胺
英文名称
3-amino-5-methoxypyridine
英文别名
5-methoxypyridin-3-amine;5-methoxy-3-aminopyridine;3-Amino-5-methoxypyridin
3-氨基-5-甲氧基吡啶化学式
CAS
64436-92-6
化学式
C6H8N2O
mdl
——
分子量
124.142
InChiKey
CTQPCFFQBYXOAJ-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

  • 熔点:
    64-65 °C(Solv: benzene (71-43-2))
  • 沸点:
    166-168 °C(Press: 15 Torr)
  • 密度:
    1.139±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    9
  • 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:
    48.1
  • 氢给体数:
    1
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2933399090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335
  • 储存条件:
    2-8°C

SDS

SDS:05ba1f3c3ab6bc5e6775fc8414bb6459
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Material Safety Data Sheet

Section 1. Identification of the substance
Product Name: 5-Methoxypyridin-3-amine
Synonyms:

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

Section 3. Composition/information on ingredients.
Ingredient name: 5-Methoxypyridin-3-amine
CAS number: 64436-92-6

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: C6H8N2O
Molecular weight: 124.1

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.

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:
    3-氨基-5-甲氧基吡啶盐酸ferrous(II) sulfate heptahydrateN-溴代丁二酰亚胺(NBS)正丁基锂硫酸 、 sodium 3-nitrobenzene sulfonate 、 硼酸过氧化苯甲酰 作用下, 以 四氢呋喃甲醇四氯化碳 为溶剂, 反应 12.0h, 生成 (3-methoxy[1,5]naphthyridin-4-yl)methyl bromide
    参考文献:
    名称:
    Process Development of a Novel Azetidinyl Ketolide Antibiotic
    摘要:
    Process development and the multikilogram synthesis of a novel azetidinyl ketolide antibiotic is described. Starting with clarithromycin, the eight-step synthesis features several telescoped operations and direct isolations, which results in a significant improvement in throughput and a major reduction in solvent usage and waste stream volume over the first scale-up campaign. Particular highlights of this effort include the development of an efficient synthesis of 3-hydroxy-1,5-naphthyridine-4-carbaldehyde via a Skraup process and engineering a robust final API synthesis. We also discovered a crystalline monotosylate salt that addressed significant formulation and degradation issues experienced when using the noncrystalline freebase.
    DOI:
    10.1021/op300064b
  • 作为产物:
    描述:
    1-苄基-3,5-哌啶二酮 在 palladium on activated charcoal 吡啶sodium hydroxide盐酸羟胺氢气 作用下, 25.0~65.0 ℃ 、405.3 kPa 条件下, 反应 1.0h, 生成 3-氨基-5-甲氧基吡啶
    参考文献:
    名称:
    Tamura, Yasumitsu; Fujita, Masanobu; Chen, Ling Ching, Heterocycles, 1981, vol. 15, # 2, p. 871 - 874
    摘要:
    DOI:
  • 作为试剂:
    描述:
    4-methoxy-1,8,10-triazatricyclo[7.4.0.02,7]trideca-2(7),3,5,8,10,12-hexaene-11-carboxylic acid 在 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium-3-oxide hexafluorophosphate 、 N,N-二异丙基乙胺3-氨基-5-甲氧基吡啶 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 16.5h, 生成 4-methoxy-N-(5-methoxypyridin-3-yl)-1,8,10-triazatricyclo[7.4.0.02,7]trideca-2(7),3,5,8,10,12-hexaene-11-carboxamide
    参考文献:
    名称:
    PROBES FOR IMAGING HUNTINGTIN PROTEIN
    摘要:
    提供了包含化合物I式的成像剂,或其药学上可接受的盐,以及它们的使用方法。
    公开号:
    US20170056535A1
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文献信息

  • [EN] 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS<br/>[FR] 1H-PYRAZOLO [4,3-B] PYRIDINES EN TANT QU'INHIBITEURS DE PDE1
    申请人:H LUNDBECK AS
    公开号:WO2018007249A1
    公开(公告)日:2018-01-11
    The present invention provides 1H-pyrazolo[4,3-b]pyridin-7-amines of formula (I) as PDE1 inhibitors and their use as a medicament, in particular for the treatment of neurodegenerative disorders and psychiatric disorders.
    本发明提供了式(I)的1H-吡唑并[4,3-b]吡啶-7-胺作为PDE1抑制剂,并将其用作药物,特别用于治疗神经退行性疾病和精神疾病。
  • MACROCYCLES AS PDE1 INHIBITORS
    申请人:H. Lundbeck A/S
    公开号:US20190185489A1
    公开(公告)日:2019-06-20
    The present invention provides macrocycles of formula (I) as PDE1 inhibitors and their use as a medicament, in particular for the treatment of neurodegenerative disorders and psychiatric disorders.
    本发明提供了式(I)的大环化合物作为PDE1抑制剂,并将其用作药物,特别用于治疗神经退行性疾病和精神疾病。
  • 1H-PYRAZOLO[4,3-B]PYRIDINES AS PDE1 INHIBITORS
    申请人:H. Lundbeck A/S
    公开号:US20190194189A1
    公开(公告)日:2019-06-27
    The present invention provides 1H-pyrazolo[4,3-b]pyridines of formula (I) as PDE1 inhibitors and their use as a medicament, in particular for the treatment of neurodegenerative disorders and psychiatric disorders.
    本发明提供了式(I)的1H-吡唑并[4,3-b]吡啶类化合物作为PDE1抑制剂,并将其用作药物,特别用于治疗神经退行性疾病和精神疾病。
  • NITROGEN-CONTAINING HETEROCYCLIC COMPOUND OR SALT THEREOF
    申请人:FUJIFILM Corporation
    公开号:US20150322063A1
    公开(公告)日:2015-11-12
    A compound represented by Formula [1] (in the formula, Z 1 represents N, CH, or the like; X 1 represents NH or the like; R 1 represents a heteroaryl group or the like; each of R 2 , R 3 , and R 4 represents a hydrogen atom, a halogen atom, an alkoxy group, or the like; and R 5 represents a heteroaryl group or the like) or salt thereof.
    由式[1]表示的化合物(在该式中,Z表示N、CH或类似物;X表示NH或类似物;R表示杂环烷基或类似物;R2、R3和R4中的每一个表示氢原子、卤原子、烷氧基或类似物;R5表示杂环烷基或类似物)或其盐。
  • [EN] 1,3 DI-SUBSTITUTED CYCLOBUTANE OR AZETIDINE DERIVATIVES AS HEMATOPOIETIC PROSTAGLANDIN D SYNTHASE INHIBITORS<br/>[FR] DÉRIVÉS D'AZÉTIDINE OU DE CYCLOBUTANE 1,3-DISUBSTITUÉS UTILISÉS COMME INHIBITEURS DE LA PROSTAGLANDINE D SYNTHASE HÉMATOPOÏÉTIQUE (H-PGDS)
    申请人:GLAXOSMITHKLINE IP DEV LTD
    公开号:WO2018069863A1
    公开(公告)日:2018-04-19
    A compound of formula (I), wherein R, R1, R2, R3, Y, Y1, a, X, and Z are as defined herein. The compounds of the present invention are inhibitors of hematopoietic prostaglandin D synthase (H-PGDS) and can be useful in the treatment of Duchenne Muscular Dystrophy. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting H-PGDS activity and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.
    式(I)的化合物,其中R、R1、R2、R3、Y、Y1、a、X和Z的定义如本文所述。本发明的化合物是造血前列腺素D合成酶(H-PGDS)的抑制剂,可用于治疗杜兴氏肌肉萎缩症。因此,本发明进一步涉及包含本发明化合物的药物组合物。本发明还进一步涉及使用本发明化合物或包含本发明化合物的药物组合物来抑制H-PGDS活性和治疗相关疾病的方法。
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