5-硝基-1H-吲哚-1-甲酸叔丁酯 | 166104-19-4

• 物质功能分类: 医药中间体 - 杂环化合物 - 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-硝基-1H-吲哚-1-甲酸叔丁酯
• 中文别名: N-Boc-5-硝基吲哚
• 英文名称: tert-butyl 5-nitro-1H-indole-1-carboxylate
• 英文别名: tert-butyl 5-nitroindole-1-carboxylate
• CAS: 166104-19-4
• 化学式: C₁₃H₁₄N₂O₄
• 分子量: 262.265
• InChiKey: GSHXPDVMVVLYLH-UHFFFAOYSA-N

物化性质

• 熔点：
  115℃

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  77
• 氢给体数：
  0
• 氢受体数：
  4

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

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: tert-butyl 5-nitroindole-1-carboxylate
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: tert-butyl 5-nitroindole-1-carboxylate
CAS number: 166104-19-4

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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: C13H14N2O4
Molecular weight: 262.3

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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-硝基-1H-吲哚-1-甲酸叔丁酯 在 potassium carbonate 作用下， 以 甲醇 、 水 为溶剂， 反应 0.25h， 以98%的产率得到5-硝基吲哚
  参考文献：
  名称：

  NH-杂芳烃的氨基甲酸叔丁酯在碱性条件下的轻度脱保护

  摘要：

  摘要 回流下的甲醇碳酸钾水溶液已被证明是吲哚、吲唑、咔唑、噻唑并吲哚和吡咯的氨基甲酸叔丁酯的高效脱保护剂。该方法是一种温和的方法，尤其适用于带有吸电子基团的 NH-杂芳烃。

  DOI：

  10.1080/00397910600634480
• 作为产物：
  描述：

  二碳酸二叔丁酯 、 5-硝基吲哚 在 吡啶 、 4-二甲氨基吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以99%的产率得到5-硝基-1H-吲哚-1-甲酸叔丁酯
  参考文献：
  名称：

  钯催化的芳基卤化锂与芳基锌酸锂的交叉偶联：异美体宁G的类似物的合成及其作为GSK-3β抑制剂的评价

  摘要：

  使用钯催化的三有机锌酸锂的交叉偶联反应已合成了异构体G的几种类似物。后者已被制备deprotonative锂化，随后使用的ZnCl转移金属化2 TMEDA（0.33当量）。 交叉偶联-杂环-钯-锌-锂

  DOI：

  10.1055/s-0029-1217003

文献信息

• [EN] AZABENZIMIDAZOLES AND THEIR USE AS AMPA RECEPTOR MODULATORS<br/>[FR] AZABENZIMIDAZOLES ET LEUR UTILISATION EN TANT QUE MODULATEURS DES RÉCEPTEURS AMPA
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2016176460A1

  公开（公告）日：2016-11-03

  Provided herein are compounds of Formula (I), and pharmaceutically acceptable salts, N-oxides, or solvates thereof, [formula (I) should be inserted here]. Also provided herein are pharmaceutical compositions comprising compounds of Formula (I) and methods of using compounds of Formula (I).

  本文件提供了公式(I)的化合物，以及药学上可接受的盐、N-氧化物或溶剂化物[此处应插入公式(I)]。此外，还提供了包含公式(I)化合物的药物组合物以及使用公式(I)化合物的方法。
• Palladium-Catalyzed Reduction of <i>N</i>-(<i>tert</i>-Butoxycarbonyl)indoles by Polymethylhydrosiloxane
  作者：Srivari Chandrasekhar、Debjit Basu、Ch. Raji Reddy

  DOI：10.1055/s-2007-966029

  日期：——

  The palladium-catalyzed [10% Pd(OH)2/C] reduction of N-(tert-butoxycarbonyl)indoles to the corresponding N-(tert-butoxy­carbonyl)indolines is described. Polymethylhydrosiloxane was used as reducing agent and the reaction proceeded smoothly at room temperature in short reaction times giving the products in good yields.

  描述了钯催化（10% Pd(OH)2/C）还原N-叔丁氧羰基吲哚为相应N-叔丁氧羰基二氢吲哚的过程。使用聚甲基氢硅氧烷作为还原剂，在室温下短时间内反应顺利进行，产率良好。
• Visible‐Light Catalyzed [1+2+2] Cycloaddition Reactions Enabled by the Formation of Methylene Nitrones
  作者：Jing Guo、Ying Xie、Wen‐Tian Zeng、Qiao‐Lei Wu、Jiang Weng、Gui Lu

  DOI：10.1002/adsc.202000858

  日期：2020.12.8

  Nitrones are key intermediates in organic synthesis. Herein, we report the first photo‐redox synthesis of methylene nitrone intermediates from nitroarenes and arylamines. The highly reactive methylene nitrones are in situ trapped by alkenes to afford various isoxazolidines. This three‐component reaction features the use of N,N‐dimethylanilines or N‐aryl glycines as C1 building blocks, which allow for

  硝基是有机合成中的关键中间体。本文中，我们报道了由硝基芳烃和芳基胺进行的光催化还原亚甲基中间体中间体。高反应性的亚甲基硝基酮被烯烃原位捕获，得到各种异恶唑烷。此三组分反应的特征是使用N，N-二甲基苯胺或N-芳基甘氨酸作为C1结构单元，可从简单的起始原料进行一锅形式的正式[1 + 2 + 2]环加成。在温和的条件下，可以以中等至良好的收率获得各种有用的异恶唑烷。机理研究支持通过选择性的N-CH 3键裂解和亚甲基转移形成亚甲基硝酮。
• Palladium-Catalyzed Cross-Couplings of Lithium Arylzincates with Aromatic Halides: Synthesis of Analogues of Isomeridianin G and Evaluation as GSK-3β Inhibitors
  作者：Florence Mongin、Anne Seggio、Ghislaine Priem、Floris Chevallier

  DOI：10.1055/s-0029-1217003

  日期：2009.11

  Several analogues of isomeridianin G have been synthesized using palladium-catalyzed cross-coupling reactions of lithium triorganozincates as a key step. The latter have been prepared by deprotonative lithiation followed by transmetalation using ZnCl2˙TMEDA (0.33 equiv). cross-coupling - heterocycles - palladium - zinc - lithium

  使用钯催化的三有机锌酸锂的交叉偶联反应已合成了异构体G的几种类似物。后者已被制备deprotonative锂化，随后使用的ZnCl转移金属化2 TMEDA（0.33当量）。 交叉偶联-杂环-钯-锌-锂
• Deprotection of N-BOC compounds
  申请人：Choy Jason Chi-Chung

  公开号：US20090203910A1

  公开（公告）日：2009-08-13

  Organic compounds having nitrogen atoms protected with t-butoxycarbonyl are effectively deprotected by heating in a fluorinated alcohol solution.

  具有叔丁氧羰基保护的含氮有机化合物可以通过在氟代醇溶液中加热来有效去保护。