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8-巯基喹啉

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8-巯基喹啉
英文名 8-Mercaptoquinoline
8-Quinolinethiol
识别
CAS号 491-33-8  checkY
PubChem 96028
ChemSpider 86692
SMILES
 
  • c1cc2cccnc2c(c1)S
InChI
 
  • 1/C9H7NS/c11-8-5-1-3-7-4-2-6-10-9(7)8/h1-6,11H
InChIKey MHTSJSRDFXZFHQ-UHFFFAOYAD
性质
化学式 C9H7NS
摩尔质量 161.22 g·mol⁻¹
外观 无色固体[1]
熔点 58.5 °C（331.6 K）[2]
沸点 296 °C（569 K）[3]
相关物质
相关化学品 8-羟基喹啉
8-氨基喹啉
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

8-巯基喹啉是一种有机化合物，化学式为C9H7NS，它是喹啉的8号位的氢被巯基取代得到的化合物。

制备

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喹啉和氯磺酸反应，得到喹啉-8-磺酰氯，它在甲苯中和三苯基膦反应，得到8-巯基喹啉。[4]

8-溴喹啉和甲硫醇钠反应，酸化后也能得到8-巯基喹啉。[5]

反应

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8-巯基喹啉可以作为螯合配体，和金属化合物反应生成相应的8-巯基喹啉配位化合物，如它和四氯合金(III)酸钠反应，可以得到8-巯基喹啉二氯化金[6]；和二氯化二(二甲基亚砜)合铂反应，生成LPtCl[SO(CH3)2]（L为8-巯基喹啉阴离子）[7]；和二氯化二乙腈合钯(II)反应，得到8-巯基喹啉钯(II)，配体中的硫和氮原子共同参与配位。[8]

8-巯基喹啉和氯化苄在碳酸钾的存在下于N,N-二甲基甲酰胺中反应，可以得到8-苄硫基喹啉。[9]它在乙醇溶液中和碘的氯仿溶液发生不可逆的氧化还原反应，生成(喹啉-8,8'-二硫化物)三碘化物，在该化合物中，喹啉𬭩阳离子通过π-π堆积相互作用形成二聚体。[10]它和溴乙烯反应，也能形成𬭩盐：[11]

它和二碘甲烷发生类似反应：[12]

参考文献

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  1. ^ Fleischer, Holger "Structural chemistry of complexes of (n - 1)d10nsm metal ions with β-N-donor substituted thiolate ligands (m=0, 2)" Coordination Chemistry Reviews 2005, volume 249, pp. 799-827. doi:10.1016/j.ccr.2004.08.024
  2. ^ Ponci, R.; Gialdi, F. Antibacterial action of quinoline derivatives. VIII. Preparation of some thiols, sulfides, and disulfides of quinoline. Farmaco, Edizione Scientifica, 1954. 9. 459-466. ISSN: 0430-0920.
  3. ^ Bankovskis, J.; Cera, L.; Ievins, A.; Luksa, E. Analytical application of 8-quinolinethiol (thiooxine) and its derivatives. XXVII. Production of anhydrous 8-mercaptoquinoline. Latvijas PSR Zinatnu Akademijas Vestis, Kimijas Serija, 1963. 2. 224-227. ISSN: 0002-3248.
  4. ^ Rao, Heng; Yu, Wen-Qian; Zheng, Hui-Qin; Bonin, Julien; Fan, Yao-Ting; Hou, Hong-Wei. Highly efficient photocatalytic hydrogen evolution from nickel quinolinethiolate complexes under visible light irradiation. Journal of Power Sources. 2016, 324: 253–260. ISSN 0378-7753. doi:10.1016/j.jpowsour.2016.05.095. 
  5. ^ Zajdel, Paweł; Marciniec, Krzysztof; Maślankiewicz, Andrzej; Grychowska, Katarzyna; Satała, Grzegorz; Duszyńska, Beata; Lenda, Tomasz; Siwek, Agata; Nowak, Gabriel; Partyka, Anna; Wróbel, Dagmara; Jastrzębska-Więsek, Magdalena; Bojarski, Andrzej J.; Wesołowska, Anna; Pawłowski, Maciej. Antidepressant and antipsychotic activity of new quinoline- and isoquinoline-sulfonamide analogs of aripiprazole targeting serotonin 5-HT1A/5-HT2A/5-HT7 and dopamine D2/D3 receptors. European Journal of Medicinal Chemistry. 2013, 60: 42–50. ISSN 0223-5234. doi:10.1016/j.ejmech.2012.11.042. 
  6. ^ Casado-Sánchez, Antonio; Martín-Santos, Cecilia; Padrón, José M.; Mas-Ballesté, Rubén; Navarro-Ranninger, Carmen; Alemán, José; Cabrera, Silvia. Effect of electronic and steric properties of 8-substituted quinolines in gold(III) complexes: Synthesis, electrochemistry, stability, interactions and antiproliferative studies. Journal of Inorganic Biochemistry. 2017, 174: 111–118. ISSN 0162-0134. doi:10.1016/j.jinorgbio.2017.06.004. 
  7. ^ Casado-Sánchez, Antonio; Uygur, Mustafa; González-Muñoz, Daniel; Aguilar-Galindo, Fernando; Nova-Fernández, José Luis; Arranz-Plaza, Judith; Díaz-Tendero, Sergio; Cabrera, Silvia; Mancheño, Olga García; Alemán, José. 8-Mercaptoquinoline as a Ligand for Enhancing the Photocatalytic Activity of Pt(II) Coordination Complexes: Reactions and Mechanistic Insights. The Journal of Organic Chemistry. 2019, 84 (10): 6437–6447. ISSN 0022-3263. doi:10.1021/acs.joc.9b00520. 
  8. ^ Moro, A. C.; Mauro, A. E.; Ananias, S. R.; Stevanato, A.; Legendre, A. O. Mono- and dinuclear palladium(II) compounds containing N,S donor ligands. Journal of Thermal Analysis and Calorimetry. 2007, 87 (3): 721–724. ISSN 1388-6150. doi:10.1007/s10973-006-7770-4. 
  9. ^ Hu, Shuai; Jin, Yi; Liu, Yanghan; Ljungman, Mats; Neamati, Nouri. Synthesis and mechanistic studies of quinolin-chlorobenzothioate derivatives with proteasome inhibitory activity in pancreatic cancer cell lines. European Journal of Medicinal Chemistry. 2018, 158: 884–895. ISSN 0223-5234. doi:10.1016/j.ejmech.2018.09.037. 
  10. ^ Chernov'yants, Margarita S.; Starikova, Zoya A.; Karginova, Anastasia O.; Kolesnikova, Tatiana S.; Tereznikov, Alexander Yu. Spectroscopic and structural investigation of interaction product of 8-mercaptoquinoline with molecular iodine. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2013, 115: 861–865. ISSN 1386-1425. doi:10.1016/j.saa.2013.06.119. 
  11. ^ Kim, J. C.; Lee, E. O.; Kim, J. D. The hemolytic characteristics of amphotericin B-containing egg PC liposomes. Yakche Hakhoechi, 1993. 23 (2): 111-118. ISSN: 0259-2347.
  12. ^ Kim, D. G.; Sokolova, S. V.; Lukina, V. V.; Volkova, S. A. Synthesis and properties of 2H-thiazolo[5,4,3-i,j]quinolinium halides. Izvestiya Vysshikh Uchebnykh Zavedenii, Khimiya i Khimicheskaya Tekhnologiya, 1993. 36 (11): 107-110. ISSN: 0579-2991.
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