791595-74-9
791595-74-9 结构式
基本信息
6-溴-1H-苯并咪唑-2-胺
5-溴-1H-苯并咪唑-2-胺
6-bromo-1H-Benzimidazol-2-amine
5-Bromo-1H-benzimidazol-2-amine
5-BROMO-1H-BENZIMIDAZOLE-2-AMINE
2-AMino-5-BroMo-1H-BenziMidazole
2-Amino-6-Bromo-1H-benzimidaZole
1H-Benzimidazol-2-amine, 6-bromo-
6-bromo-1H-1,3-benzodiazol-2-amine
2-AMINO-5(6)-BROMO-1H-BENZIMIDAZOLE
6-bromo-1H-benzo[d]imidazol-2-amine
物理化学性质
安全数据
制备方法
506-68-3
1575-37-7
791595-74-9
步骤A: 合成5-溴-1H-苯并咪唑-2-胺 [00400] 将4-溴-1,2-苯二胺(4g,21.39mmol)溶于甲醇(20mL)中,形成深棕色溶液。向该溶液中加入溴化氰(2.492g,23.52mmol)。反应过程中放热,几秒钟后甲醇开始沸腾。反应5分钟后,用乙酸乙酯(100mL)稀释反应混合物,依次用饱和碳酸氢钠水溶液(100mL)和饱和氯化钠溶液(100mL)洗涤。将有机层浓缩至几毫升后,通过硅胶柱色谱法(0-20%甲醇/乙酸乙酯梯度洗脱)纯化,得到5-溴-1H-苯并咪唑-2-胺(3.9g,18.39mmol,产率86%)为黑色固体。 1H NMR (400 MHz, DMSO-d6) δ ppm: 6.47 (br.s., 2H), 6.94-7.00 (m, 1H), 7.01-7.06 (m, 1H), 7.23 (d, J = 1.85 Hz, 1H), 8.70-11.33 (m, 1H); ES LC-MS m/z = 212.2 (Br 79, M + H)+, ES LC-MS m/z = 214.2 (Br 81, M + H)+.
参考文献:
[1] Angewandte Chemie - International Edition, 2012, vol. 51, # 21, p. 5226 - 5229
[2] Patent: US2013/136782, 2013, A1. Location in patent: Paragraph 0216; 0217
[3] Patent: WO2012/174312, 2012, A2. Location in patent: Page/Page column 283-284
[4] Patent: WO2008/42282, 2008, A2. Location in patent: Page/Page column 219-220
[5] Advanced Synthesis and Catalysis, 2018, vol. 360, # 10, p. 1943 - 1948
