未明确具体用途,主要用于医药相关领域(基于参考文献推测)。
医药
合成路线 1(2. 合成:793-19-1)
产率:100%
合成条件:at 20℃; for 8 h; Reflux
实验步骤:在室温下,将苄胺(10.7g,0.1mol)的MeOH(50mL)溶液逐滴加入到丙烯酸甲酯(18.9g,0.022mol)的MeOH(100mL)溶液中。 将得到的混合物回流8小时,真空蒸发,得到27.9g产物,定量收率。 'H-NIVIR(400MHz,CDCl 3):7.28(m,5H),3.64(s,2H),3.59(s,6H),2.80(m,4H),2.47(m,4H)。
参考文献:
- [1] Patent: WO2017/15106, 2017, A1. Location in patent: Page/Page column 30 [2] Journal of Labelled Compounds and Radiopharmaceuticals, 2013, vol. 56, # 14, p. 722 - 725 [3] Planta Medica, 2017, vol. 83, # 5, p. 420 - 425 [4] Patent: US2017/274362, 2017, A1. Location in patent: Paragraph 0077-0079 [5] Patent: EP2570410, 2013, A1. Location in patent: Paragraph 0062 [6] Patent: US2013/231369, 2013, A1. Location in patent: Paragraph 0100 [7] Patent: CN106187863, 2016, A. Location in patent: Paragraph 0135; 0136; 0137 [8] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 8, p. 2161 - 2165 [9] Patent: EP1548016, 2005, A1. Location in patent: Page/Page column 15 [10] Synthetic Communications, 2007, vol. 37, # 18, p. 3143 - 3149 [11] Russian Journal of Organic Chemistry, 2003, vol. 39, # 1, p. 49 - 56 [12] Synthetic Communications, 2006, vol. 36, # 6, p. 795 - 801 [13] RSC Advances, 2018, vol. 8, # 9, p. 4531 - 4547 [14] Journal of the American Chemical Society, 1950, vol. 72, p. 3298 [15] Journal of pharmaceutical sciences, 1972, vol. 61, # 11, p. 1739 - 1745 [16] Journal of Heterocyclic Chemistry, 1990, vol. 27, # 7, p. 1885 - 1892 [17] Journal of Organic Chemistry, 2000, vol. 65, # 24, p. 8367 - 8371 [18] Journal of Heterocyclic Chemistry, 2013, vol. 50, # 6, p. 1374 - 1380 [19] Molecules, 2018, vol. 23, # 9,