化学合成。
化学合成; 寡核苷酸合成; 多肽合成
合成路线 1(1. 合成:51644-96-3)
产率:72%
合成条件:at 20℃; for 4.50 h; Cooling with ice
实验步骤:一般程序:在30分钟内,将二碳酸二叔丁酯(22g,100mmol)的MeOH(20mL)溶液加入搅拌的1,4-二氨基丁烷(25,1.8g,20mmol)的MeOH溶液中( 在冰冷却下160mL)。 在室温下搅拌4小时后,减压除去溶剂。 通过硅胶柱色谱法(CHCl 3:MeOH:aq.NH 3 = 10:1:0.1)纯化残余物,得到标题化合物(26),收率83%。
参考文献:
- [1] European Journal of Organic Chemistry, 1998, # 5, p. 853 - 859 [2] ACS Medicinal Chemistry Letters, 2017, vol. 8, # 6, p. 614 - 617 [3] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 20, p. 7145 - 7155 [4] Journal of Medicinal Chemistry, 2004, vol. 47, # 20, p. 4933 - 4940 [5] Chemical and Pharmaceutical Bulletin, 2015, vol. 63, # 5, p. 326 - 333 [6] Organic and Biomolecular Chemistry, 2012, vol. 10, # 27, p. 5258 - 5265 [7] Journal of Medicinal Chemistry, 1997, vol. 40, # 16, p. 2643 - 2652 [8] Tetrahedron Letters, 1996, vol. 37, # 4, p. 551 - 554 [9] Bulletin of the Korean Chemical Society, 2010, vol. 31, # 11, p. 3353 - 3358 [10] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 21, p. 5740 - 5743 [11] Patent: WO2008/136631, 2008, A1. Location in patent: Page/Page column 5; 12-13 [12] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2005, vol. 60, # 1, p. 89 - 98 [13] Journal of Medicinal Chemistry, 1989, vol. 32, # 2, p. 391 - 396 [14] Journal of Medicinal Chemistry, 1998, vol. 41, # 13, p. 2175 - 2179 [15] European Journal of Medicinal Chemistry, 2004, vol. 39, # 11, p. 975 - 988 [16] Journal of Organic Chemistry, 2005, vol. 70, # 16, p. 6230 - 6241 [17] Patent: US4604378, 1986, A [18] Patent: US4826813, 1989, A [19] Journal of Medicinal Chemistry, 2008, vol. 51, # 15, p. 4388 - 4391 [20] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 17, p. 6354 - 6359 [21] Chinese Chemical Letters, 2014, vol. 25, # 12, p. 1545 - 1549 [22] Patent: WO2014/202775, 2014, A1. Location in patent: Sheet 14/33 [23] Chemical Biology and Drug Design, 2015, vol. 85, # 2, p. 145 - 152 [24] Bioorganic Chemistry, 2018, vol. 80, p. 649 - 654