3-氰基-1H-吲哚-6-羧酸甲酯 | 1000576-51-1

• 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: 3-氰基-1H-吲哚-6-羧酸甲酯
• 中文别名: 吲哚-6-甲酸甲酯-3-甲腈
• 英文名称: methyl 3-cyano-1H-indole-6-carboxylate
• CAS: 1000576-51-1
• 化学式: C₁₁H₈N₂O₂
• 分子量: 200.197
• InChiKey: YBZVEPCMUWGFNW-UHFFFAOYSA-N

物化性质

• 沸点：
  413.5±25.0 °C(Predicted)
• 密度：
  1.33±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  65.9
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2933990090
• 危险性防范说明：
  P280,P305+P351+P338
• 危险性描述：
  H302
• 储存条件：
  2-8°C

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: Methyl 3-cyanoindole-6-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: Methyl 3-cyanoindole-6-carboxylate
CAS number: 1000576-51-1

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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.
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: C11H8N2O2
Molecular weight: 200.2

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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

制备方法与用途

吲哚-6-甲酸甲酯-3-甲腈常用于有机合成和医药中间体等领域。

反应信息

• 作为反应物：
  描述：

  3-氰基-1H-吲哚-6-羧酸甲酯 在 吡啶 、 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 硼酸三异丙酯 、 potassium carbonate 、 caesium carbonate 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 生成 Methyl 3-cyano-1-ethyl-2-[4-(ethylsulfonylamino)phenyl]indole-6-carboxylate
  参考文献：
  名称：

  发现N-（4'-（吲哚-2-基）苯基）磺酰胺作为HCV复制的新型抑制剂

  摘要：

  合成了一系列新颖的2-苯基吲哚类似物，并在亚基因组HCV复制子抑制试验中评估了其活性。鉴定了几种在苯环上含有小烷基磺酰胺的化合物，它们相对于基因型1b复制子表现出亚微摩尔EC 50值。其中， 相对于细胞毒性，化合物25d有效抑制1b复制子（EC 50 = 0.17μM），选择性为147倍。化合物25d在人肝微粒体存在下稳定，在大鼠中具有良好的药代动力学特征，IV半衰期为4.3小时，口服生物利用度（F）为58％。

  DOI：

  10.1016/j.bmcl.2013.04.050
• 作为产物：
  描述：

  吲哚-6-甲酸甲酯 、 苯乙腈 在 copper(l) iodide 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 34.0h， 以82%的产率得到3-氰基-1H-吲哚-6-羧酸甲酯
  参考文献：
  名称：

  用苄基氰化物作为氰化物阴离子替代物对吲哚的氰化

  摘要：

  已经实现了用苄基氰化物作为氰化物阴离子替代物对吲哚进行铜介导的直接氰化。该级联反应在温和的反应条件下提供了3-氰基吲哚，具有良好的收率和优异的产率，并具有各种官能团耐受性。

  DOI：

  10.1016/j.tet.2013.03.089

文献信息

• Cyanation of indoles with benzyl cyanide as the cyanide anion surrogate
  作者：Lianpeng Zhang、Qiaodong Wen、Jisong Jin、Chen Wang、Ping Lu、Yanguang Wang

  DOI：10.1016/j.tet.2013.03.089

  日期：2013.5

  A copper-mediated direct cyanation of indoles with benzyl cyanide as the cyanide anion surrogate has been achieved. The cascade reaction furnished 3-cyanoindoles under mild reaction conditions in good to excellent yields with various functional groups tolerance.

  已经实现了用苄基氰化物作为氰化物阴离子替代物对吲哚进行铜介导的直接氰化。该级联反应在温和的反应条件下提供了3-氰基吲哚，具有良好的收率和优异的产率，并具有各种官能团耐受性。
• Discovery of N-(4′-(indol-2-yl)phenyl)sulfonamides as novel inhibitors of HCV replication
  作者：Guangming Chen、Hongyu Ren、Anthony Turpoff、Alexander Arefolov、Richard Wilde、James Takasugi、Atiyya Khan、Neil Almstead、Zhengxian Gu、Takashi Komatsu、Connie Freund、Jamie Breslin、Joseph Colacino、Jean Hedrick、Marla Weetall、Gary M. Karp

  DOI：10.1016/j.bmcl.2013.04.050

  日期：2013.7

  A series of novel 2-phenylindole analogs were synthesized and evaluated for activity in subgenomic HCV replicon inhibition assays. Several compounds containing small alkyl sulfonamides on the phenyl ring exhibiting submicromolar EC50 values against the genotype 1b replicon were identified. Among these, compound 25d potently inhibited the 1b replicon (EC50 = 0.17 μM) with 147-fold selectivity with respect

  合成了一系列新颖的2-苯基吲哚类似物，并在亚基因组HCV复制子抑制试验中评估了其活性。鉴定了几种在苯环上含有小烷基磺酰胺的化合物，它们相对于基因型1b复制子表现出亚微摩尔EC 50值。其中， 相对于细胞毒性，化合物25d有效抑制1b复制子（EC 50 = 0.17μM），选择性为147倍。化合物25d在人肝微粒体存在下稳定，在大鼠中具有良好的药代动力学特征，IV半衰期为4.3小时，口服生物利用度（F）为58％。