悉尼酮
| 悉尼酮 | |
|---|---|
| |
| IUPAC名 2H-Oxadiazol-5-one | |
| 别名 | 1,2,3-Oxadiazol-5(2H)-one |
| 识别 | |
| CAS号 | 534-24-7 
|
| PubChem | 12443168 |
| ChemSpider | 65792731 |
| SMILES |
|
| 性质 | |
| 化学式 | C2H2N2O2 |
| 摩尔质量 | 86.05 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
悉尼酮是一类含有第5位置有酮基的1,2,3-𫫇二唑的介离子杂环化合物。 [1][2][3] 跟其他介离子化合物一样，它们具有双极性。它们拥有正电荷和负电荷，在环上离域。根据近期[何时？]的电脑计算，悉尼酮和其他类似的介离子化合物不具有芳香性，“却通过电子和电荷离域在两个不同的区域里有良好的稳定性”。[4]悉尼酮的名称来自悉尼。
悉尼酮的酮基（=O）被亚胺基（=NH）取代，形成悉尼酮亚胺。它们出现于兴奋剂feprosidnine和美索卡的子结构里。
发现
[编辑]悉尼酮首次由Earl和Mackney于1935年制备，通过用乙酸酐将N-亚硝基-N-苯甘胺酸脱水环化制造。[5]后期工作表明这个方法通常可以应用于N-取代的氨基酸的亚硝胺。[2]
化学结构
[编辑]
参见
[编辑]参考文献
[编辑]- ^ 国际纯化学和应用化学联合会，化学术语概略，第二版。（金皮书）(1997)。在线校正版: (2006–) "sydnones"。doi:10.1351/goldbook.S05990
- ^ 2.0 2.1 Stewart, F. H. C. The Chemistry of the Sydnones. Chemical Reviews. 1 April 1964, 64 (2): 129–147. doi:10.1021/cr60228a004.
- ^ Browne, Duncan L.; Harrity, Joseph P.A. Recent developments in the chemistry of sydnones. Tetrahedron. January 2010, 66 (3): 553–568. doi:10.1016/j.tet.2009.10.085.
- ^ Simas, Alfredo. Are mesoionic compounds aromatic?. Canadian Journal of Chemistry. 1998, 76: 869–872. doi:10.1139/v98-065.
- ^ Earl, J. Campbell; Mackney, Alan W. 204. The action of acetic anhydride on N-nitrosophenylglycine and some of its derivatives. Journal of the Chemical Society (Resumed). 1935: 899. doi:10.1039/jr9350000899.
- S. Wiechmann; T. Freese; M. H. H. Drafz; E. G. Hübner; J. C. Namyslo; M. Nieger; A. Schmidt. Sydnone anions and abnormal N-heterocyclic carbenes of O-ethylsydnones. Characterizations, calculations and catalyses.. Chem. Commun. 2014, 50: 11822–11824. doi:10.1039/C4CC05461J
. - Claude V. Greco; Wayne H. Nyberg; C. C. Cheng . Synthesis of Sydnones and Sydnone Imines. Journal of Medicinal Chemistry. 1962, 5 (4): 861–865. doi:10.1021/jm01239a022.
- Wilson Baker; W. D. Ollis. Meso-ionic compounds. Quarterly Reviews, Chemical Society. 1957, 11: 15–30. doi:10.1039/QR9571100015.
- Joseph Fugger; Jack M. Tien; I. Moyer Hunsberger . The Preparation of Substituted Hydrazines. I. Alkylhydrazines via Alkylsydnones. J. Am. Chem. Soc. 1955, 77 (7): 1843–1848. doi:10.1021/ja01612a039.
- Jack M. Tien ; I. Moyer Hunsberger . The Preparation of Substituted Hydrazines. II.1 3-Pyridylhydrazine via the Phototropic N-(3-Pyridyl)-sydnone. J. Am. Chem. Soc. 1955, 77 (24): 6604–6607. doi:10.1021/ja01629a052. 88, 178 (1961);
- Jack M. Tien ; I. Moyer Hunsberger . Sydnones. III. Preparation and Interconversion of Mercurated Derivatives of N-(3-Pyridyl)-sydnone1-3a. J. Am. Chem. Soc. 1961, 83 (1): 178–182. doi:10.1021/ja01462a035.
- Alan R. Katritzky. Chem. Ind. . 1955: 521 . 缺少或
|title=为空 (帮助) - Alexander Lawson ; D. H. Miles . Some new mesoionic compounds. J. Chem. Soc. . 1959: 2865–2871. doi:10.1039/JR9590002865.
- J. Ogilvie; V. K. Miyamoto; Thomas C. Bruice. A Kinetic Study of the Reaction of a "Meso-ionic" Compound (Dehydrodithizone) with Haloacetates. J. Am. Chem. Soc. 1961, 83 (11): 2493–2495. doi:10.1021/ja01472a017.
- LEMONT B. KIER, LAURETTA E. FOX, D. DHAWAN & I. W. WATERS. A New Class of Central Nervous System Stimulants. Nature. 1962, 195 (4843): 817–818. Bibcode:1962Natur.195..817K. PMID 14455827. doi:10.1038/195817a0.
