3-吡咯烷-1-苯胺 | 115833-93-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 中文名称: 3-吡咯烷-1-苯胺
• 中文别名: 3-(1-吡咯烷基)苯胺
• 英文名称: 3-(pyrrolidin-1-yl)aniline
• 英文别名: N-m-aminophenylpyrrolidine；3-pyrrolidin-1-ylaniline
• CAS: 115833-93-7
• 化学式: C₁₀H₁₄N₂
• mdl: MFCD05259334
• 分子量: 162.235
• InChiKey: DNPBFTQZONVQDX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  12
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  29.3
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 危险等级：
  IRRITANT
• 危险品标志：
  Xi
• 海关编码：
  2933990090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 3-(Pyrrolidin-1-yl)aniline
Synonyms:

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

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Section 3. Composition/information on ingredients.
Ingredient name: 3-(Pyrrolidin-1-yl)aniline
CAS number: 115833-93-7

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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.
Store in closed vessels, refrigerated.
Storage:

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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
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C10H14N2
Molecular weight: 162.2

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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
Non-harzardous for air and ground transportation.

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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

反应信息

• 作为反应物：
  描述：

  3-吡咯烷-1-苯胺 在 硫酸 、 sodium nitrite 作用下， 以 水 为溶剂， 反应 16.0h， 以94.4%的产率得到3-(1-吡咯烷)苯酚
  参考文献：
  名称：

  间二烷胺基苯酚的合成方法

  摘要：

  间二烷胺基苯酚的合成方法，其特征为：第一步，将间二烷胺基酰基苯胺和硫酸水溶液混合均匀并加热至50~110℃，保温反应得到含间二烷胺基苯胺的硫酸水溶液；第二步，继续滴加亚硝酸钠水溶液，亚硝酸钠水溶液的滴加温度为‑10~20℃，滴毕于5~30℃保温，得到含间二烷胺基苯胺重氮盐的硫酸水溶液；第三步，含间二烷胺基苯胺重氮盐的硫酸水溶液直接加热至45~110℃，保温，发生重氮盐的水解反应，冷却后处理，得产物间二烷胺基苯酚；三步反应所需的硫酸在第一步反应中一次性投加完毕；三步反应在一锅内分步完成。本发明方法具有原料价格低廉、来源充足，合成工艺安全性高，产品收率高，三废污染较少等特点，具有较高工业化价值。

  公开号：

  CN109134281B
• 作为产物：
  描述：

  1-(3-硝基苯基)-吡咯烷 在 palladium on activated charcoal 氢气 作用下， 以 甲醇 、 乙酸乙酯 为溶剂， 反应 2.5h， 以100%的产率得到3-吡咯烷-1-苯胺
  参考文献：
  名称：

  苯氧乙酸衍生物的合成作为胃泌素/胆囊收缩素-B受体的强效拮抗剂。二。

  摘要：

  合成了一系列苯氧基乙酰苯胺衍生物，并评估了它们对人胃泌素/胆囊收缩素（CCK）-B和CCK-A受体的拮抗活性。在合成的化合物中，2- [3- [3- [N- [2-（N-甲基-N-苯基氨基甲酰基甲氧基）苯基] -N-（N-甲基-N-苯基氨基甲酰基甲基）氨基甲酰基甲基]-脲基]苯基]乙酸（20i，DA-3934）对胃泌素/ CCK-B受体表现出高亲和力，对CCK-A受体表现出高选择性。DA-3934及其甲酯衍生物以剂量依赖的方式抑制大鼠五肽胃泌素诱导的胃酸分泌。

  DOI：

  10.1248/cpb.46.951

文献信息

• スクアリリウム化合物
  申请人：株式会社日本触媒

  公开号：JP2017179131A

  公开（公告）日：2017-10-05

  【課題】極性溶媒中での安定性に優れたスクアリリウム化合物とこれを含む溶液および樹脂組成物を提供する。【解決手段】下記式（１）で表されることを特徴とするスクアリリウム化合物。［式（１）中、Ｒ1〜Ｒ8はそれぞれ独立して、水素原子、有機基または極性官能基を表し、Ａ1およびＡ2はそれぞれ独立して、カルボニル基またはスルホニル基を表し、Ｘは有機連結基を表す。］【選択図】図１

  【课题】提供在极性溶剂中稳定性优异的司卡利亚化合物及其包含的溶液和树脂组成物。【解决手段】特征为由下式（1）表示的司卡利亚化合物。［在式（1）中，R1至R8分别独立表示氢原子、有机基或极性官能团，A1和A2分别独立表示羧基或磺酰基，X表示有机连接基。］【选择图】图1
• Dipyrimidine Amines: A Novel Class of Chemokine Receptor Type 4 Antagonists with High Specificity
  作者：Aizhi Zhu、Weiqiang Zhan、Zhongxing Liang、Younghyoun Yoon、Hua Yang、Hans E. Grossniklaus、Jianguo Xu、Mauricio Rojas、Mark Lockwood、James P. Snyder、Dennis C. Liotta、Hyunsuk Shim

  DOI：10.1021/jm100786g

  日期：2010.12.23

  The C-X-C chemokine receptor type 4 (CXCR4)/stromal cell derived factor-1 (SDF-1 or CXCL12) interaction and the resulting cell signaling cascade play a key role in metastasis and inflammation. On the basis of the previously published CXCR4 antagonist 5 (WZ811), a series of novel nonpeptidic anti-CXCR4 small molecules have been designed and synthesized to improve potency. Following a structure−activity

  CXC 趋化因子受体 4 (CXCR4)/基质细胞衍生因子-1（SDF-1 或 CXCL12）相互作用和由此产生的细胞信号级联反应在转移和炎症中起关键作用。在先前发表的 CXCR4 拮抗剂5 (WZ811)的基础上，设计并合成了一系列新型非肽类抗 CXCR4 小分子以提高效力。根据大约5的结构-活性特征，发现了N , N '-(1, 4-亚苯基双(亚甲基)) dipyrimidin-2-amines 系列中更先进的化合物，并且显示出比5具有更高的 CXCR4 结合潜力和特异性。化合物26(508MCl) 是先导化合物，在三种体外试验中表现出亚纳摩尔的效力，包括竞争性结合、基质胶侵入和 Gα i环磷酸腺苷 (cAMP) 调节信号。此外，化合物26通过干扰三种小鼠模型中的 CXCR4 功能显示出有希望的效果：爪子炎症、Matrigel 栓塞血管生成和葡萄膜黑色素瘤微转移。这些数据表明，双嘧啶胺是独特的具有高效力和特异性的
• <i>N</i>-(1-Oxy-2-picolyl)oxalamic Acid as an Efficient Ligand for Copper-Catalyzed Amination of Aryl Iodides at Room Temperature
  作者：Yongbin Wang、Jing Ling、Yu Zhang、Ao Zhang、Qizheng Yao

  DOI：10.1002/ejoc.201500279

  日期：2015.7

  N-(1-Oxy-pyridin-2-ylmethyl)oxalamic acid was identified as efficient ligand for CuI-catalyzed amination of aryl halides at room temperature. In our catalytic system, N-arylation of cyclic secondary amines, primary amines, amino acids, and ammonia proceeded with moderate to excellent yields and high functional group tolerance.

  N-(1-Oxy-pyridin-2-ylmethyl) 草氨酸被确定为室温下 CuI 催化的芳基卤化物胺化的有效配体。在我们的催化系统中，环状仲胺、伯胺、氨基酸和氨的 N-芳基化以中等至优异的产率和高官能团耐受性进行。
• Phenylenediamine urotensin-II receptor antagonists and CCR-9 antagonists
  申请人：Wu Chengde

  公开号：US20050049286A1

  公开（公告）日：2005-03-03

  The present invention relates to urotensin II receptor antagonists, CCR-9 antagonists, pharmaceutical compositions containing them and their use.

  这项发明涉及尿泉素II受体拮抗剂、CCR-9拮抗剂、含有它们的药物组合物以及它们的用途。
• Noncatalytic Electrophilic Oxyalkylation of Anilines with 2-Trifluoroacetyl-1,3-benzothiazole
  作者：Pavel Mykhailiuk、Pavel Khodakovskiy、Dmitriy Volochnyuk、Andrey Tolmachev

  DOI：10.1055/s-0029-1218712

  日期：2010.5

  3-benzothiazole reacts with anilines to form the corresponding trifluoromethyl-substituted alcohols. The reaction regioselectivity (ortho/para) was shown to depend strongly on the structure of the aniline. meta-Substituted anilines tend to form the corresponding ortho-substituted products, in contrary to the previous literature data. anilines - Friedel-Crafts alkylation - ortho/para-substitution - trifluoromethyl

  2-三氟乙酰基-1,3-苯并噻唑与苯胺反应形成相应的三氟甲基取代的醇。反应区域选择性（邻位/对位）显示出强烈依赖于苯胺的结构。与先前的文献数据相反，间位取代的苯胺倾向于形成相应的邻位取代的产物。 苯胺-Friedel-Crafts烷基化-邻位/对位取代-三氟甲基醇-1,3-苯并噻唑