5-甲氧基吲哚啉 | 21857-45-4

• 物质功能分类: 医药中间体 - 吲哚类化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 中文名称: 5-甲氧基吲哚啉
• 英文名称: 5-methoxyindoline
• 英文别名: 5-methoxy-2,3-dihydro-1H-indole
• CAS: 21857-45-4
• 化学式: C₉H₁₁NO
• 分子量: 149.192
• InChiKey: YYDYAQAVAHKFJO-UHFFFAOYSA-N

物化性质

• 沸点：
  282.6±29.0 °C(Predicted)
• 密度：
  1.076±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  21.3
• 氢给体数：
  1
• 氢受体数：
  2

安全信息

• 海关编码：
  2933990090
• 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：
  | 2-8°C |

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 5-Methoxy-2,3-dihydroindoline
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: 5-Methoxy-2,3-dihydroindoline
CAS number: 21857-45-4

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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: C9H11NO
Molecular weight: 149.2

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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：

  5-甲氧基吲哚啉 在 五氧化二碘 作用下， 以 二甲基亚砜 为溶剂， 以67%的产率得到5-甲氧基靛红
  参考文献：
  名称：

  一种基于吲哚的高效方法，利用I 2 O 5作为氧化剂合成靛红

  摘要：

  已经探索了以高收率利用无机高价I 2 O 5合成基于吲哚的靛红的有效方法，该方法成功地实现了在无金属，温和条件下，在广泛的底物范围内从吲哚向靛红的转化。

  DOI：

  10.1016/j.tetlet.2017.03.060
• 作为产物：
  描述：

  5-甲氧基吲哚 在 sodium cyanoborohydride 、 溶剂黄146 作用下， 反应 2.0h， 以90%的产率得到5-甲氧基吲哚啉
  参考文献：
  名称：

  供体-受体Stenhouse加合物的光致异构化途径上的亮点

  摘要：

  供体-受体Stenhouse加合物（DASA）是负性光致变色材料，在各种应用中都具有广阔的前景。优化其开关特性的关键是对光开关机制的详细了解，但目前尚无。在这里，我们描述了DASA光开关及其主要中间体的光化步骤，并结合了超快可见光和IR泵浦光谱仪和TD-DFT计算进行了研究。将时间分辨的红外光谱与DFT计算进行比较，可以清楚地确定中间体的结构，从而确认光吸收会诱导顺序反应路径，其中C 2 –C 3的Z–E光异构化随后是围绕C的旋转3 –C4和随后的热环化步骤。第一代和第二代DASA在氯化溶剂中具有共同的光异构化机制，在激发态的动力学和寿命方面存在显着差异。第二代DASA的光生中间体在低温下光聚集，并用时间分辨光谱进行探测，证明了异构化过程的光可逆性。综上所述，这些结果在分子水平上提供了DASA异构化途径的详细描述。

  DOI：

  10.1021/jacs.7b09081
• 作为试剂：
  描述：

  对硝基苯甲醛 、 水杨酰肼 在 5-甲氧基吲哚啉 作用下， 以 aq. phosphate buffer 、 N,N-二甲基甲酰胺 为溶剂， 生成 N'-[(4-nitrophenyl)methylidene]-2-hydroxybenzohydrazide
  参考文献：
  名称：

  在中性条件下，吲哚啉催化酰基//肟缩合。

  摘要：

  酰基hydr的形成已广泛应用于材料科学和生物标记中。然而，它们在中性条件下的凝结速率缓慢，限制了其应用。在本文中，具有电子给体基团的二氢吲哚被报道为新的催化剂支架，其可以通过亚胺离子中间体催化酰基hydr，和肟的形成。在中性条件下，这种新型催化剂显示出比传统苯胺催化反应高出15倍的速率增强。鉴定出的二氢吲哚催化剂已成功应用于水凝胶的形成。

  DOI：

  10.1021/acs.orglett.0c02128

文献信息

• Npy antagonists, preparation and uses
  申请人：Botez Iuliana

  公开号：US20090233910A1

  公开（公告）日：2009-09-17

  The present invention concerns novel compounds, their preparation and their uses, therapeutic uses in particular. More specifically it concerns derivative compounds having at least two aromatic cycles, their preparation and their uses, in particular in the area of human or animal health. These compounds have an affinity for the biological receptors of neuropeptide Y, NPY, present in the central and peripheral nervous systems. The compounds of the invention are preferably NPY antagonists, and more particularly antagonists of sub-type NPY Y1, and can therefore be used for the therapeutic or prophylactic treatment of any disorder involving NPY. The present invention also concerns pharmaceutical compositions containing said compounds, their preparation and their uses, as well as treatment methods using said compounds.

  本发明涉及新颖化合物，它们的制备和用途，特别是在治疗方面的用途。更具体地说，它涉及至少具有两个芳香环的衍生化合物，它们的制备和用途，特别是在人类或动物健康领域。这些化合物对存在于中枢和外周神经系统中的神经肽Y（NPY）的生物受体具有亲和力。本发明的化合物优选为NPY拮抗剂，更具体地说是NPY Y1亚型的拮抗剂，因此可用于治疗或预防涉及NPY的任何疾病。本发明还涉及含有所述化合物的药物组合物，其制备和用途，以及使用所述化合物的治疗方法。
• Flavin/I₂ -Catalyzed Aerobic Oxidative C-H Sulfenylation of Aryl-Fused Cyclic Amines
  作者：Xinpeng Jiang、Zongchen Zhao、Zhifeng Shen、Keda Chen、Liyun Fang、Chuanming Yu

  DOI：10.1002/ejoc.202000508

  日期：2020.7.7

  A metal‐free aerobic oxidative C–H sulfenylation of aryl‐fused cyclic amines with various thiols was developed with excellent functional compatibility. While flavin I catalyzed the C–H sulfenylation of indolines to afford 3‐sulfenylindoles, flavin II enabled transformations resulting in substitution at the position para to the N atom on the aryl ring to obtain 6‐sulfenylquinolines.

  芳基稠合的环胺与各种硫醇的无金属好氧氧化C–H亚磺酰化反应具有出色的功能相容性。虽然黄素我催化的二氢吲哚的C-H亚磺酰化，得到3- sulfenylindoles，黄素II启用导致取代在位置变换对位到Ñ在芳环上原子，得到6- sulfenylquinolines。
• Ru(<scp>ii</scp>)-Catalyzed C7-acyloxylation of indolines with carboxylic acids
  作者：Pinaki Bhusan De、Sonbidya Banerjee、Sourav Pradhan、Tharmalingam Punniyamurthy

  DOI：10.1039/c8ob01603h

  日期：——

  Ruthenium-catalyzed site-selective C7-acyloxyation of indolines with carboxylic acids is presented that can be oxidized to indoles with diverse functional groups.

  铑催化的选择性C7-酰氧化反应将吲哚与羧酸进行作用，可氧化为具有多种功能基团的吲哚化合物。
• Divergent Dehydrogenative Coupling of Indolines with Alcohols
  作者：Xue Jiang、Weijun Tang、Dong Xue、Jianliang Xiao、Chao Wang

  DOI：10.1021/acscatal.6b03667

  日期：2017.3.3

  The dehydrogenative coupling of indolines with alcohols catalyzed by an iridium complex has been achieved to afford both N- and C3-alkylated indoles selectively, by simply changing the addition time of a base additive. The iridacycle catalyst plays multiple roles in these reactions, which dehydrogenates both amines and alcohols and catalyzes the coupling reactions. Mechanistic studies reveal that a

  通过简单地改变基础添加剂的添加时间，已经实现了二氢吲哚与被铱络合物催化的醇的脱氢偶联，从而选择性地提供了N-和C3-烷基化的吲哚。iridacycle催化剂在这些反应中起多种作用，使胺和醇都脱氢并催化偶联反应。机理研究表明，借用氢-脱氢过程和脱氢-借入氢过程分别涉及N-烷基化和C3-烷基化反应。C3-烷基化反应涉及两个sp3碳中心的直接偶联。
• A General Method for N-Methylation of Amines and Nitro Compounds with Dimethylsulfoxide
  作者：Xue Jiang、Chao Wang、Yawen Wei、Dong Xue、Zhaotie Liu、Jianliang Xiao

  DOI：10.1002/chem.201303802

  日期：2014.1.3

  DMSO methylates a broad range of amines in the presence of formic acid, providing a novel, green and practical method for amine methylation. The protocol also allows the one‐pot transformation of aromatic nitro compounds into dimethylated amines in the presence of a simple iron catalyst.

  DMSO在甲酸存在下将多种胺甲基化，为胺甲基化提供了一种新颖，绿色且实用的方法。该协议还允许在简单的铁催化剂存在下将芳香族硝基化合物单锅转化为二甲基化胺。

表征谱图