吲嗪-2-甲酸甲酯
外觀
![本頁使用了標題或全文手工轉換](http://upload.wikimedia.org/wikipedia/commons/thumb/c/cd/Zh_conversion_icon_m.svg/35px-Zh_conversion_icon_m.svg.png)
吲嗪-2-甲酸甲酯 | |
---|---|
![]() | |
識別 | |
CAS編號 | 16959-62-9 ![]() |
性質 | |
化學式 | C10H9NO2 |
摩爾質量 | 175.18 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
吲嗪-2-甲酸甲酯是一種有機化合物,化學式為C10H9NO2,它是吲嗪2號位的氫被甲氧羰基取代的產物。它可由β-羥基-α-亞甲基(吡啶-2-基)丙酸甲酯和乙酸酐回流(或和三甲基矽基重氮甲烷在室溫反應[1])得到。[2]它在鹼中水解,酸化後可以得到吲嗪-2-甲酸。[3]在碳酸銫和鈀催化下,它和3-氟氯苯反應,可以得到3-(3-氟苯基)吲嗪-2-甲酸甲酯。[4]
參考文獻
[編輯]- ^ Liusheng Zhu, Marc Vimolratana, Sean P. Brown, Julio C. Medina. A mild preparation of substituted indolizines and indole from simple aromatic precursors using (trimethylsilyl)diazomethane. Tetrahedron Letters. 2008-03, 49 (11): 1768–1770 [2022-10-10]. doi:10.1016/j.tetlet.2008.01.067. (原始內容存檔於2018-06-17) (英語).
- ^ Khethobole C Sekgota, Michelle Isaacs, Heinrich C Hoppe, Ronnett Seldon, Digby F Warner, Setshaba D Khanye, Perry T Kaye. Propylphosphonic acid anhydride–mediated amidation of Morita–Baylis–Hillman–derived indolizine-2-carboxylic acids. Journal of Chemical Research. 2021-07, 45 (7-8): 674–678 [2022-10-10]. ISSN 1747-5198. doi:10.1177/1747519820987156. (原始內容存檔於2022-10-17) (英語).
- ^ Saraghina M. D. Cunha, Ramon G. de Oliveira, Mário L. A. A. Vasconcellos. Microwave-assisted convenient syntheses of 2-indolizine derivatives from Morita-Baylis-Hillman adducts: new in silico potential ion channel modulators. Journal of the Brazilian Chemical Society. 2013-03, 24 (3): 432–438 [2022-10-10]. ISSN 0103-5053. doi:10.1590/S0103-50532013000300011. (原始內容存檔於2018-06-02) (英語).
- ^ Bo Liu, Zhi Wang, Ningjie Wu, Mingliang Li, Jingsong You, Jingbo Lan. Discovery of a Full-Color-Tunable Fluorescent Core Framework through Direct CH (Hetero)arylation of N-Heterocycles. Chemistry - A European Journal. 2012-02-06, 18 (6): 1599–1603 [2022-10-10]. doi:10.1002/chem.201103329 (英語).