2-氨基-4-氰基吡啶 | 42182-27-4

• 物质功能分类: 医药中间体 - 吡啶类化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 中文名称: 2-氨基-4-氰基吡啶
• 中文别名: 2-氨基异烟腈
• 英文名称: 4-cyanopyridin-2-amine
• 英文别名: 2-amino-isonicotinonitrile；2-amino-4-cyanopyridine；2-aminopyridine-4-carbonitrile；4-cyano-2-aminopyridine
• CAS: 42182-27-4
• 化学式: C₆H₅N₃
• mdl: MFCD03791310
• 分子量: 119.126
• InChiKey: GEEAYLFEIFJFGP-UHFFFAOYSA-N

物化性质

• 熔点：
  146-148°C
• 沸点：
  297.7±20.0 °C(Predicted)
• 密度：
  1.23±0.1 g/cm3(Predicted)
• 稳定性/保质期：

  常规情况下不会分解，也没有危险反应。

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  9
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  62.7
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 危险等级：
  6.1
• 危险品标志：
  Xi
• 安全说明：
  S26,S36/37/39
• 危险类别码：
  R20/21/22,R36/37/38
• 海关编码：
  2933399090
• 危险品运输编号：
  3439
• 危险类别：
  6.1
• 包装等级：
  III
• 危险性防范说明：
  P261,P280,P301+P312,P302+P352,P304+P340,P305+P351+P338,P312,P332+P313,P337+P313
• 危险性描述：
  H302,H312,H315,H319,H332
• 储存条件：
  密封、阴凉、干燥处保存。

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 2-Amino-4-cyanopyridine
Synonyms:

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H302: Harmful if swallowed
H315: Causes skin irritation
H318: Causes serious eye damage
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
P280: Wear protective gloves/protective clothing/eye protection/face protection
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing

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Section 3. Composition/information on ingredients.
Ingredient name: 2-Amino-4-cyanopyridine
CAS number: 42182-27-4

---

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.

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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.

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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.

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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.
Storage: Store in closed vessels.

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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.

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Section 9. Physical and chemical properties
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C6H5N3
Molecular weight: 119.1

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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.

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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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.

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Section 14. Transportation information
UN Number: UN3439 Class: 6.1 Packing group: III
Proper shipping name: NITRILES, TOXIC, SOLID, N.O.S. (2-Amino-4-cyanopyridine)

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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.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

氨基吡啶及其衍生物 用途

氨基吡啶是一种重要的精细化工中间体，广泛应用于医药和农药等领域。其中，2-氨基-4-氰基吡啶作为mGluR2拮抗剂，可用于治疗中枢神经系统疾病。

合成方法

合成2-氨基-4-氰基吡啶的方法多样：

1. 以2-氨基吡啶为原料，依次经过氮氧化反应、硝化反应、氨基保护、还原反应、席曼反应以及氨基脱保护反应制备。此路线涉及多个危险的化学反应步骤，且合成路径较长，总收率较低。

2. 另一种方法是使用2-氯-4-氰基吡啶为起始物料与氨水发生氨解反应来制备目标化合物。

3. 还可以采用2-硝基-4-氰基吡啶经铁粉还原的方法进行合成。

相关化学反应方程式如下图所示：


反应信息

• 作为反应物：
  描述：

  2-氨基-4-氰基吡啶 在 四(三苯基膦)钯 盐酸 、 N-溴代丁二酰亚胺(NBS) 、 sodium carbonate 、 肼 、 sodium nitrite 作用下， 以 1,4-二氧六环 、 乙二醇二甲醚 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 42.0h， 生成 6-(2,4-dichloro-phenyl)-[1,2,4]triazolo[4,3-a]pyridine-7-carbonitrile
  参考文献：
  名称：

  WO2007/113226

  摘要：

  公开号：
• 作为产物：
  描述：

  2-氨基吡啶 在 吡啶 、 sodium periodate 、 硫酸 、 碘 、 溶剂黄146 作用下， 以 水 为溶剂， 反应 4.5h， 生成 2-氨基-4-氰基吡啶
  参考文献：
  名称：

  [EN] ORGANIC COMPOUNDS
  [FR] COMPOSÉS ORGANIQUES

  摘要：

  揭示了新型苯并呋喃衍生物。这些衍生物具有S1P1受体活性和/或疾病修饰活性，并可用于治疗与动物和/或人类的免疫、血管和神经系统相关的疾病或症状。

  公开号：

  WO2014063199A1
• 作为试剂：
  描述：

  2-((4-Methoxybenzyl)amino)isonicotinonitrile 在 水 、 乙酸乙酯 、 ethyl acetate petroleum ether 、 2-氨基-4-氰基吡啶 作用下， 以 三氟乙酸 为溶剂， 反应 3.0h， 以This resulted in 1.8 g (crude) of 2-aminoisonicotinonitrile as a yellow solid的产率得到2-氨基-4-氰基吡啶
  参考文献：
  名称：

  BORON-CONTAINING SMALL MOLECULES

  摘要：

  本发明涉及6-取代苯并氧硼烷化合物等物品，以及它们用于治疗细菌感染的用途。

  公开号：

  US20110212918A1

文献信息

• Fragment-to-Hit-to-Lead Discovery of a Novel Pyridylurea Scaffold of ATP Competitive Dual Targeting Type II Topoisomerase Inhibiting Antibacterial Agents
  作者：Gregory S. Basarab、John I. Manchester、Shanta Bist、P. Ann Boriack-Sjodin、Brian Dangel、Ruth Illingworth、Brian A. Sherer、Shubha Sriram、Maria Uria-Nickelsen、Ann E. Eakin

  DOI：10.1021/jm401208b

  日期：2013.11.14

  The discovery and optimization of a new class of bacterial topoisomerase (DNA gyrase and topoisomerase IV) inhibitors binding in the ATP domain are described. A fragment molecule, 1-ethyl-3-(2-pyridyl)urea, provided sufficiently potent enzyme inhibition (32 μM) to prompt further analogue work. Acids and acid isosteres were incorporated at the 5-pyridyl position of this fragment, bridging to a key asparagine

  描述和发现了一种新型的结合在ATP域中的细菌拓扑异构酶（DNA促旋酶和拓扑异构酶IV）抑制剂。片段分子1-乙基-3-（2-吡啶基）脲提供了足够强的酶抑制作用（32μM），可促进进一步的类似工作。在该片段的5-吡啶基位置掺入了酸和酸等排体，桥接至关键的天冬酰胺残基，改善了酶抑制作用，并产生了可测量的抗菌活性。由于有利的亲脂性相互作用，在4-吡啶基位置的CF 3-噻唑取代基改善了抑制能力。与革兰氏阳性病原体金黄色葡萄球菌和肺炎链球菌相比，具有良好的抗菌活性和革兰氏阴性病原流感嗜血杆菌和卡他莫拉菌。前体代谢物的掺入和突变分析研究支持双分子拓扑异构酶抑制作用的作用方式，DNA合成的阻断。化合物35在小鼠金黄色葡萄球菌疾病模型中是有效的，其中证明了菌落形成单位相对于对照减少了4.5个对数。
• Metal-Free Regioselective Alkylation of Imidazo[1,2-a]pyridines with N-Hydroxyphthalimide Esters under Organic Photoredox Catalysis
  作者：Can Jin、Bin Sun、Tengwei Xu、Liang Zhang、Rui Zhu、Jin Yang、Min Xu

  DOI：10.1055/s-0039-1691567

  日期：2020.3

  A visible-light-induced direct C–H alkylation of imidazo[1,2-a]pyridines has been developed. It proceeds at room temperature by employing inexpensive Eosin Y as a photocatalyst and alkyl N-hydroxyphthalimide (NHP) esters as alkylation reagents. A variety of NHP esters derived from aliphatic carboxylic acids (primary, secondary, and tertiary) were tolerated in this protocol, giving the corresponding

  已开发出可见光诱导的咪唑并 [1,2-a] 吡啶直接 C-H 烷基化。它通过使用廉价的曙红 Y 作为光催化剂和烷基 N-羟基邻苯二甲酰亚胺 (NHP) 酯作为烷基化试剂在室温下进行。该协议允许使用源自脂肪族羧酸（初级、二级和三级）的各种 NHP 酯，从而以中等至极好的收率提供相应的 C-5 烷基化产品。机理研究表明，该过程涉及自由基脱羧偶联途径。
• FLAP MODULATORS
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：US20150259357A1

  公开（公告）日：2015-09-17

  The present invention relates to compounds of Formula (I), or a form thereof, wherein ring A, R 1 , R 2 , R 3 , R 3 ′, L, W, and V are as defined herein, useful as FLAP modulators. The invention also relates to pharmaceutical compositions comprising compounds of Formula (I). Methods of making and using the compounds of Formula (I) are also within the scope of the invention

  本发明涉及式（I）的化合物，或其形式，其中环A，R1，R2，R3，R3'，L，W和V如本文所定义，可用作FLAP调节剂。该发明还涉及包含式（I）化合物的药物组合物。制备和使用式（I）化合物的方法也属于本发明的范围。
• [EN] AZAINDAZOLES AS BTK KINASE MODULATORS AND USE THEREOF<br/>[FR] AZAINDAZOLES COMME MODULATEURS DE LA KINASE BTK ET LEUR UTILISATION
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2011019780A1

  公开（公告）日：2011-02-17

  Compounds having the formula (I), and enantiomers, and diastereomers, pharmaceutically-acceptable salts, thereof, (I) are useful as kinase modulators, including Btk modulation, wherein A1, A2, A3, R4, are as defined herein.

  具有化学式(I)的化合物，以及其对映体、非对映异构体、药用可接受的盐，(I)可用作激酶调节剂，包括Btk调节，在此处定义了A1、A2、A3、R4。
• 苯并咪唑类衍生物及其药学用途
  申请人：上海美悦生物科技发展有限公司

  公开号：CN110343089A

  公开（公告）日：2019-10-18

  本发明公开了一种苯并咪唑类衍生物及其药学用途，特别是公开了一种如式I所示的苯并咪唑类衍生物及其在制备治疗和/或预防血栓形成或血栓栓塞病症的药物中的用途。