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对二乙胺基吡啶 | 36075-06-6

中文名称
对二乙胺基吡啶
中文别名
2-二乙氨基吡啶;二乙基氨基吡啶;2-二乙基氨基吡啶
英文名称
2-(diethylamino)pyridine
英文别名
N,N-diethylpyridin-2-amine;2-Diethylaminopyridine
对二乙胺基吡啶化学式
CAS
36075-06-6
化学式
C9H14N2
mdl
MFCD00059777
分子量
150.224
InChiKey
XRPITCBWOUOJTH-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:
    118 °C / 27mmHg
  • 密度:
    0.97
  • 稳定性/保质期:
    如果遵照规格使用和储存,则不会分解,未有已知危险反应。

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.444
  • 拓扑面积:
    16.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933399090
  • 储存条件:
    请将贮藏器密封,并存放在阴凉、干燥处。同时,确保工作环境有良好的通风或排气设施。

SDS

SDS:29ea2ac6003a398d3efca57db640a070
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2-Diethylaminopyridine
SAFETY DATA SHEET

Section 1. IDENTIFICATION
Product name: 2-Diethylaminopyridine

Section 2. HAZARDS IDENTIFICATION
GHS classification
PHYSICAL HAZARDS
Category 4
Flammable liquids
HEALTH HAZARDS Not classified
Not classified
ENVIRONMENTAL HAZARDS
GHS label elements, including precautionary statements
None
Pictograms or hazard symbols
Signal word Warning
Combustible liquid
Hazard statements
Precautionary statements:
Keep away from flames and hot surfaces.
[Prevention]
Wear protective gloves and eye/face protection.
Store in a well-ventilated place. Keep cool.
[Storage]
[Disposal] Dispose of contents/container through a waste management company authorized by
the local government.

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substance/mixture: Substance
Components: 2-Diethylaminopyridine
>97.0%(T)
Percent:
CAS Number: 36075-06-6
N-(2-Pyridyl)diethylamine
Synonyms:
Chemical Formula: C9H14N2

Section 4. FIRST AID MEASURES
Inhalation: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
Get medical advice/attention if you feel unwell.
Skin contact: Remove/Take off immediately all contaminated clothing. Rinse skin with
water/shower. If skin irritation or rash occurs: Get medical advice/attention.
Eye contact: Rinse cautiously with water for several minutes. Remove contact lenses, if present
and easy to do. Continue rinsing. If eye irritation persists: Get medical
advice/attention.
Get medical advice/attention if you feel unwell. Rinse mouth.
Ingestion:
Protection of first-aiders: A rescuer should wear personal protective equipment, such as rubber gloves and air-
tight goggles.
2-Diethylaminopyridine

Section 5. FIRE-FIGHTING MEASURES
Suitable extinguishing Dry chemical, foam, carbon dioxide.
media:
Unsuitable extinguishing Water (It may scatter and spread fire.)
media:
Specific hazards arising Take care as it may decompose upon combustion or in high temperatures to
from the chemical: generate poisonous fume.
Precautions for firefighters: Fire-extinguishing work is done from the windward and the suitable fire-extinguishing
method according to the surrounding situation is used. Uninvolved persons should
evacuate to a safe place. In case of fire in the surroundings: Remove movable
containers if safe to do so.
Special protective When extinguishing fire, be sure to wear personal protective equipment.
equipment for firefighters:

Section 6. ACCIDENTAL RELEASE MEASURES
Use personal protective equipment. Keep people away from and upwind of spill/leak.
Personal precautions,
protective equipment and Ensure adequate ventilation. Entry to non-involved personnel should be controlled
emergency procedures: around the leakage area by roping off, etc.
Environmental precautions: Prevent product from entering drains.
Methods and materials for Absorb spilled material in a suitable absorbent (e.g. rag, dry sand, earth, saw-dust).
containment and cleaning In case of large amount of spillage, contain a spill by bunding. Adhered or collected
up: material should be promptly disposed of, in accordance with appropriate laws and
regulations.
Prevention of secondary Remove all sources of ignition. Fire-extinguishing devices should be prepared in
hazards: case of a fire. Use spark-proof tools and explosion-proof equipment.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Technical measures: Handling is performed in a well ventilated place. Wear suitable protective equipment.
Prevent generation of vapour or mist. Keep away from flames and hot surfaces. Take
measures to prevent the build up of electrostatic charge. Use explosion-proof
equipment. Wash hands and face thoroughly after handling.
Use a closed system, ventilation.
Advice on safe handling: Avoid contact with skin, eyes and clothing.
Conditions for safe storage, including any
incompatibilities
Keep container tightly closed. Store in a cool, dark and well-ventilated place.
Storage conditions:
Store away from incompatible materials such as oxidizing agents.
Comply with laws.
Packaging material:

Section 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
Engineering controls: Install a closed system or local exhaust as possible so that workers should not be
exposed directly. Also install safety shower and eye bath.
Personal protective equipment
Respiratory protection: Vapor respirator. Follow local and national regulations.
Hand protection: Protective gloves.
Safety glasses. A face-shield, if the situation requires.
Eye protection:
Skin and body protection: Protective clothing. Protective boots, if the situation requires.

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Physical state (20°C): Liquid
Clear
Form:
Colour: Pale yellow - Greyish reddish yellow
No data available
Odour:
pH: No data available
Melting point/freezing point:No data available
Boiling point/range: 118°C/3.6kPa
Flash point: No data available
2-Diethylaminopyridine

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Flammability or explosive
limits:
Lower: No data available
Upper: No data available
Relative density: 0.97
Solubility(ies):
[Water] No data available
No data available
[Other solvents]

Section 10. STABILITY AND REACTIVITY
Chemical stability: Stable under proper conditions.
Possibility of hazardous No special reactivity has been reported.
reactions:
Conditions to avoid: Open flame
Incompatible materials: Oxidizing agents
Hazardous decomposition Carbon monoxide, Carbon dioxide, Nitrogen oxides (NOx)
products:

Section 11. TOXICOLOGICAL INFORMATION
Acute Toxicity: No data available
Skin corrosion/irritation: No data available
Serious eye No data available
damage/irritation:
Germ cell mutagenicity: No data available
Carcinogenicity:
IARC = No data available
No data available
NTP =
Reproductive toxicity: No data available

Section 12. ECOLOGICAL INFORMATION
Ecotoxicity:
Fish: No data available
Crustacea: No data available
Algae: No data available
Persistence / degradability: No data available
Bioaccumulative No data available
potential(BCF):
Mobility in soil
Log Pow: No data available
Soil adsorption (Koc): No data available
Henry's Law No data available
constant(PaM3/mol):

Section 13. DISPOSAL CONSIDERATIONS
Recycle to process, if possible. Consult your local regional authorities. You may be able to burn in a chemical
incinerator equipped with an afterburner and scrubber system. Observe all federal, state and local regulations when
disposing of the substance.

Section 14. TRANSPORT INFORMATION
Hazards Class: Does not correspond to the classification standard of the United Nations
UN-No: Not listed

Section 15. REGULATORY INFORMATION
Safe management ordinance of dangerous chemical product (State Council announces on January 26, 2002
and revised on February 16,2011): Safe use and production, the storage of a dangerous chemical, transport,
loading and unloading were prescribed.
2-Diethylaminopyridine


SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

  • 作为反应物:
    描述:
    对二乙胺基吡啶silver(II) fluoride 作用下, 以 乙腈 为溶剂, 反应 1.0h, 以75%的产率得到N,N-diethyl-6-fluoropyridin-2-amine
    参考文献:
    名称:
    受经典胺化反应启发的吡啶和二嗪的选择性 CH 氟化
    摘要:
    氟化吡啶 将氟取代基附加到碳中心通常用于调节药物和农业化学研究中的小分子特性。然而,氟化通常需要使用腐蚀性、危险的试剂。Fier 和 Hartwig (p. 956) 提出了一种异常温和且方便的方案,用于氟化吡啶和相关含氮芳烃中与氮相邻的碳位点。该反应需要用二氟化银处理并在室温下快速进行。温和的氟化方法可以帮助生产医学研究中感兴趣的化合物。氟化杂环广泛存在于药物、农用化学品和材料中。然而,将氟结合到杂芳烃中的反应范围有限并且可能是危险的。我们提出了一种广泛适用且安全的方法,用于使用市售的氟化银 (II) 对吡啶和二嗪中的单个碳氢键进行位点选择性氟化。反应在环境温度下在 1 小时内发生,并且对氮附近的氟化具有唯一的选择性。温和的条件允许获得具有重要医学意义的化合物的氟化衍生物,以及通过随后的氟化物亲核置换制备的一系列 2-取代吡啶。机理研究表明,经典的吡啶胺化途径可适用于广泛范围的氮杂环的选择性氟化。反应在环境温度下在
    DOI:
    10.1126/science.1243759
  • 作为产物:
    描述:
    2-diethylamino-5-iodopyridine 在 盐酸indium 作用下, 以 为溶剂, 反应 10.0h, 以53%的产率得到对二乙胺基吡啶
    参考文献:
    名称:
    Dehalogenation and Barbier-Type Hydroxyalkylation of π-Deficient Haloheterocycles Using Indium
    摘要:
    The reaction of pi-deficient haloheterocycles with indium metal in water gave corresponding dehalogenated heterocycles. The use of diluted hydrochloric acid instead of water accelerated the reductive reactivity of indium metal. Furthermore, Barbier-type additions proceeded by reactions of alpha-iodoheterocycles with indium in the presence of pivalaldehyde.
    DOI:
    10.3987/com-08-s(f)95
  • 作为试剂:
    描述:
    4-羟基-3,5-二甲基苯甲酸对二乙胺基吡啶 吡啶氯化亚砜 、 sodium chloride 、 碳酸氢钠三乙胺 作用下, 以 二氯甲烷 为溶剂, 生成 1,10-bis(3',5'-dimethyl-4'-acetoxyphenyl-carbonyl)-1,10-diaza-4,7,13,16-tetraoxacyclooctadecane
    参考文献:
    名称:
    US6087502
    摘要:
    公开号:
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文献信息

  • Transition-Metal-Free Amination of Pyridine-2-sulfonyl Chloride and Related <i>N</i>-Heterocycles Using Magnesium Amides
    作者:Moritz Balkenhohl、Cyril François、Daniela Sustac Roman、Pauline Quinio、Paul Knochel
    DOI:10.1021/acs.orglett.6b03703
    日期:2017.2.3
    A new transition-metal-free amination of pyridine-2-sulfonyl chloride and related N-heterocycles using magnesium amides of type R2NMgCl·LiCl is reported. Additionally, the directed ortho-magnesiation of pyridine-2-sulfonamides using TMPMgCl·LiCl was investigated. Reaction of the magnesium intermediates with various electrophiles and subsequent amination using magnesium amides led to a range of 2,3-functionalized
    的吡啶-2-磺酰氯的新过渡金属-自由胺化和相关Ñ -heterocycles使用类型R的镁酰胺2 NMgCl·LiCl报道。另外,研究了使用TMPMgCl·LiCl对吡啶-2-磺酰胺的定向邻位放大。镁中间体与各种亲电试剂的反应以及随后使用氨基酰胺进行的胺化反应产生了一系列的2,3-官能化吡啶。另外,进行提供氮杂吲哚和氮杂咔唑的环化反应。
  • Modulators of Cystic Fibrosis Transmembrane Conductance Regulator
    申请人:VERTEX PHARMACEUTICALS INCORPORATED
    公开号:US20160095858A1
    公开(公告)日:2016-04-07
    The present invention features a compound of formula I: or a pharmaceutically acceptable salt thereof, where R 1 , R 2 , R 3 , W, X, Y, Z, n, o, p, and q are defined herein, for the treatment of CFTR mediated diseases, such as cystic fibrosis. The present invention also features pharmaceutical compositions, method of treating, and kits thereof.
    本发明涉及一种具有以下化学式I的化合物: 或其药用可接受的盐,其中R 1 ,R 2 ,R 3 ,W,X,Y,Z,n,o,p和q在此处定义,用于治疗CFTR介导的疾病,如囊性纤维化。本发明还涉及药物组合物、治疗方法和相关工具包。
  • Amination of 2‐Pyridinesulfonic and 8‐Quinolinesulfonic Acids with Magnesium Amides
    作者:Moritz Balkenhohl、Vasiliki Valsamidou、Paul Knochel
    DOI:10.1002/ejoc.201900057
    日期:2019.9
    The amination of 2‐pyridine‐ and 8‐quinolinesulfonic acids using magnesium amides is reported. Various amides reacted with N‐heterocyclic sulfonic acids, leading to aminopyridines and aminoquinolines in up to 98 % yield. Various amines important in medicinal chemistry, such as the antidepressant amoxapine, were suitable for these aminations.
    据报道,使用酰胺化氨基的2-吡啶基和8-喹啉磺酸被胺化。各种酰胺与N-杂环磺酸反应,生成氨基吡啶和氨基喹啉,产率高达98%。在药物化学中很重要的各种胺,例如抗抑郁药阿莫沙平,都适合于这些胺化反应。
  • PROCESS FOR THE SYNTHESIS OF RAMELTEON AND ITS INTERMEDIATES
    申请人:Kansal Vinod Kumar
    公开号:US20090281176A1
    公开(公告)日:2009-11-12
    A process for the preparation of ramelteon and intermediates useful in the process. The process suitable for industrial scale provides increased yield and/or greater purity with fewer process steps.
    一种用于制备拉莫替昔的方法和在该过程中有用的中间体。这种适用于工业规模的方法提供了更高的产量和/或更高的纯度,且步骤更少。
  • Acyclic tertiary amines as nucleophiles in substitution reactions of aromatic and heteroaromatic halides
    作者:Kiyoshi Matsumoto、Shiro Hashimoto、Shinichi Otani
    DOI:10.1039/c39910000306
    日期:——
    Even acyclic tertiary amines such as triethylamine, tri-n-propylamine and tri-n-butylamine, which have been believed to be inert to aromatic and heteroaromatic halides, underwent SNAr reactions with aromatic and heteroaromatic halides to give the dialkylamino derivatives; in the case of monocyclic amines like N-methylpyrrolidine and N-methylpiperidine, the dealkylation being regioselective.
    甚至被认为对芳族和杂芳族卤化物呈惰性的无环叔胺,如三乙胺,三正丙胺和三正丁胺,也与芳族和杂芳族卤化物进行S N Ar反应,得​​到二烷基氨基衍生物;在单环的胺等的情况下Ñ -甲基吡咯烷和Ñ甲基哌啶,脱烷基化区域选择性被。
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