3,4-二氫-2-喹喔啉酮
| 3,4-二氫-2-喹喔啉酮 | |
|---|---|
| |
| 識別 | |
| CAS號 | 59564-59-9 
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| SMILES |
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| 性質 | |
| 化學式 | C8H8N2O |
| 摩爾質量 | 148.16 g·mol−1 |
| 外觀 | 灰白色固體[1]或米黃色固體[2] |
| 熔點 | 136~138 °C[2] |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
3,4-二氫-2-喹喔啉酮是一種有機化合物，化學式為C8H8N2O。它可用於IHCH-7113的合成。[3]
合成與反應
它可由N-(2-硝基苯基)甘氨酸甲酯和連二亞硫酸鈉在二甲基亞碸中反應得到，[1]或由鄰苯二胺和氯乙酸在氨水中加熱製得。[4]
參考文獻
- ^ 1.0 1.1 Pankaj Gupta, Surabhi Panday, Amitava Hazra, and Joydev K. Laha. Metal- and Additive-Free Intramolecular Direct Amidation of Ester Functionality within a Nitroarene Framework: Facile Access to Azaheterocycles. ACS Sustainable Chem. Eng. 2023, 11, 48, 17031–17037. doi:10.1021/acssuschemeng.3c05103.
- ^ 2.0 2.1 Pavan Sudheer Akula, Bor-Cherng Hong and Gene-Hsiang Lee. Visible-light-induced C(sp3)–H activation for a C–C bond forming reaction of 3,4-dihydroquinoxalin-2(1H)-one with nucleophiles using oxygen with a photoredox catalyst or under catalyst-free conditions. RSC Adv., 2018,8, 19580-19584. doi:10.1039/C8RA03259A.
- ^ Robichaud, Albert J.; Lee, Taekyu; Deng, Wei; Mitchell, Ian S.; Yang, Michael G.; Haydar, Simon; Chen, Wenting; McClung, Christopher D.; Calvello, Emilie J.; Zawrotny, David M. Substituted heterocycle fused gamma-carbolines. 2004. US20040220178.
- ^ Mohammed K. Ibrahim, Ibrahim H. Eissa, Abdallah E. Abdallah, Ahmed M. Metwaly, M.M. Radwan, M.A. ElSohly. Design, synthesis, molecular modeling and anti-hyperglycemic evaluation of novel quinoxaline derivatives as potential PPARγ and SUR agonists. Bioorganic & Medicinal Chemistry. 2017. 25 (4). doi:10.1016/j.bmc.2017.01.015.
- ^ Shuocheng Wan, Jie Wang, Congde Huo. Copper catalyzed aerobic oxidative amination of 3,4-dihydroquinoxalin-2(1H)-ones. Tetrahedron Letters, 2021. 78. doi:10.1016/j.tetlet.2021.153271.