3-(吡咯啉-1-基磺酰)砒啶 | 26103-51-5

• 物质功能分类: 原料药 - 人工合成抗感染类药 - 磺胺类药及增效剂
• 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: 3-(吡咯啉-1-基磺酰)砒啶
• 中文别名: 3-(吡咯啉-1-基磺酰)吡啶
• 英文名称: 3-(pyrrolidin-1-ylsulfonyl)pyridine
• 英文别名: 3-pyrrolidin-1-ylsulfonylpyridine
• CAS: 26103-51-5
• 化学式: C₉H₁₂N₂O₂S
• 分子量: 212.272
• InChiKey: MXJUPPYEPZUGLP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  58.6
• 氢给体数：
  0
• 氢受体数：
  4

安全信息

• 危险品标志：
  Xi
• 海关编码：
  2935009090

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
Product Name: 3-(Pyrrolidin-1-ylsulfonyl)pyridine
Synonyms: 3-(1-pyrrolidinylsulfonyl)pyridine; 1-(Pyridin-3-ylsulfonyl)pyrrolidine

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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-ylsulfonyl)pyridine
CAS number: 26103-51-5

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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: C9H12N2O2S
Molecular weight: 212.3

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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, sulfur 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：

  vinylidene-1,1-diphosphonic acid 、 3-(吡咯啉-1-基磺酰)砒啶 以 水 为溶剂， 反应 2.0h， 以66%的产率得到Hydroxy-[1-phosphono-2-(3-pyrrolidin-1-ylsulfonylpyridin-1-ium-1-yl)ethyl]phosphinate
  参考文献：
  名称：

  Activity of Nitrogen-Containing and Non-Nitrogen-Containing Bisphosphonates on Tumor Cell Lines

  摘要：

  We synthesized and tested three series of bisphosphonates for their activity in inhibiting the growth of three human tumor cell lines: MCF-7 (breast), NCI-H460 (lung), and SF-268 (CNS). The first series of compounds consisted of 49 nitrogen-containing bisphosphonates, the most active species being a tetrakispivaloyloxymethyl (POM) ester, having an (average) IC50 of 6.8 mu M. The second series of compounds consisted of nine terphenylbisphosphonates, the most active species also being a POM ester, having an IC50 of 2.2 mu M. The third series of compounds consisted of seven halogen or cyanophenylbisphosphonates, the most active species again being a POM ester, having an IC50 of 500 nM. Taken together, these results are of interest because they show that bisphosphonate esters can have potent activity against a variety of tumor cell lines, with the most active terphenyl-and halophenyl-containing species having IC50 values similar to 10-40x lower than the most potent commercially available bisphosphonates.

  DOI：

  10.1021/jm060280e
• 作为产物：
  描述：

  3-吡啶磺酸 在 五氯化磷 作用下， 以 苯 为溶剂， 反应 3.5h， 生成 3-(吡咯啉-1-基磺酰)砒啶
  参考文献：
  名称：

  Regioselective Lithiation of 3-Pyridylsulfonic Acid Derivatives: A Convenient Route to Various New 4-Substituted 3-Pyridylsulfonamides

  摘要：

  DOI：

  10.1055/s-1983-30528

文献信息

• Iodine-catalyzed sulfonylation of sulfonyl hydrazides with <i>tert</i>-amines: a green and efficient protocol for the synthesis of sulfonamides
  作者：Jinyang Chen、Xiaoran Han、Lan Mei、Jinchuan Liu、Kui Du、Tuanwu Cao、Qiang Li

  DOI：10.1039/c9ra07361b

  日期：——

  This study provides a direct, sustainable and eco-friendly method for the synthesis of various sulfonamides via the sulfonylation of sulfonyl hydrazides with tert-amines. The method utilizes sulfonyl hydrazides to oxidize and couple with tertiary amines through selective cleavage of C–N bonds. In this reaction, molecular iodine was used as the catalyst and t-butyl hydroperoxide was used as the oxidant

  该研究为通过磺酰肼与叔胺磺酰化合成各种磺胺类药物提供了一种直接、可持续和环保的方法。该方法利用磺酰肼氧化并通过选择性裂解 C-N 键与叔胺偶联。在该反应中，分子碘用作催化​​剂，叔丁基过氧化氢用作氧化剂。
• TBAI-catalyzed selective synthesis of sulfonamides and β-aryl sulfonyl enamines: coupling of arenesulfonyl chlorides and sodium sulfinates with <i>tert</i>-amines
  作者：Hongmei Jiang、Xiaoyue Tang、Zhihui Xu、Huixian Wang、Kang Han、Xiaolan Yang、Yuanyuan Zhou、Yong-Lai Feng、Xian-Yong Yu、Qingwen Gui

  DOI：10.1039/c8ob02992j

  日期：——

  A simple, practical and metal-free method has been developed for the synthesis of sulfonamides and β-arylsulfonyl enamines via the selective cleavage of C–N and C–H bonds through the iodine-catalyzed oxidation of arenesulfonyl chlorides and sodium sulfinates with tert-amines. The method uses commercially available inexpensive catalysts and oxidants, and has a wide substrate scope and operational simplicity

  一种简单，实用和不含金属的方法已被开发用于磺酰胺和β-芳基磺酰基的烯胺的合成通过的C-N和C-H键的选择性裂解通过芳烃磺酰基氯化物和钠基亚磺酸盐的碘催化氧化用叔-胺类。该方法使用可商购的廉价催化剂和氧化剂，并且具有广泛的底物范围和操作简便性。
• Facile One-Pot Synthesis of Aromatic and Heteroaromatic Sulfonamides
  作者：Rina Pandya、Takashi Murashima、Livio Tedeschi、Anthony G. M. Barrett

  DOI：10.1021/jo034643j

  日期：2003.10.1

  A series of arene and heteroarene sulfonamides were prepared in one vessel from aryl and heteroaryl bromides via conversion into the corresponding Grignard reagents using either magnesium or isopropylmagnesium chloride and subsequent reaction with sulfur dioxide, sulfuryl chloride, and an amine.

  在一个容器中，由芳基和杂芳基溴化物通过使用镁或异丙基氯化镁转化为相应的格氏试剂，然后与二氧化硫，硫酰氯和胺反应，制备了一系列芳烃和杂芳基磺酰胺。
• DABCO-<i>Bis</i>(sulfur dioxide), DABSO, as a Convenient Source of Sulfur Dioxide for Organic Synthesis: Utility in Sulfonamide and Sulfamide Preparation
  作者：Holly Woolven、Carlos González-Rodríguez、Isabel Marco、Amber L. Thompson、Michael C. Willis

  DOI：10.1021/ol201957n

  日期：2011.9.16

  The charge-transfer complex generated from the combination of DABCO and sulfur dioxide, DABSO, is a bench-stable colorless solid suitable for use in organic synthesis as a replacement for gaseous sulfur dioxide. The complex can be combined with Grignard reagents to form sulfinates, which can then be converted in situ to a series of sulfonamides. Alternatively, reaction with anilines and iodine leads

  由DABCO和二氧化硫（DABSO）的组合产生的电荷转移络合物是适合于有机合成的气态稳定的无色固体，可替代气态二氧化硫。该配合物可以与格氏试剂结合形成亚磺酸盐，然后可以将其原位转化为一系列磺酰胺。备选地，与苯胺和碘的反应导致一系列磺酰胺的形成。在DABSO和2，3-二甲基丁二烯之间进行加溶剂提供相应的环丁砜。
• BREANT, P.;MARSAIS, F.;QUEGUINER, G., SYNTHESIS, BRD, 1983, N 10, 822-824
  作者：BREANT, P.、MARSAIS, F.、QUEGUINER, G.

  DOI：——

  日期：——