26663-77-4
26663-77-4 结构式
基本信息
苯并咪唑-5-甲酸甲酯
苯并[D]咪唑-5 - 羧酸甲酯
苯并咪唑-5-甲酸甲酯(CAS号:26663-77-4)
5-(Methoxycarbonyl)benziMidazole
Methyl 5-BenziMidazolecarboxylate
METHYL BENZIMIDAZOLE-5-CARBOXYLATE
MethylBenzimidazole-5-carboxylate>
METHYL 1H-BENZIMIDAZOLE-5-CARBOXYLATE
methyl 1H-benzo[d]imidazole-6-carboxylate
methyl 1H-benzo[d]imidazole-5-carboxylate
5-BenziMidazolecarboxylic Acid Methyl Ester
Benzimidazole-5-carboxylic acid methyl ester
物理化学性质
制备方法
67-56-1
15788-16-6
26663-77-4
以甲醇和1H-苯并咪唑-5-羧酸为原料合成苯并咪唑-5-甲酸甲酯的一般步骤: (a)甲基1H-苯并咪唑-5-羧酸酯的合成 将亚硫酰氯(0.135 mL,1.85 mmol)缓慢滴加到1H-苯并咪唑-5-羧酸(0.300 g,1.85 mmol)的甲醇(50.0 mL)溶液中。将反应混合物回流12小时。反应完成后,将混合物倒入饱和碳酸氢钠水溶液中,充分搅拌。分离有机层,水层用乙酸乙酯(3×15 mL)萃取。合并有机层,用无水硫酸镁干燥,过滤,减压浓缩,得到紫色固体产物,收率为90%。粗产物无需进一步纯化即可用于后续反应。[MS (ES+) m/e 177 [M + H]+]。
参考文献:
[1] Patent: WO2005/82901, 2005, A1. Location in patent: Page/Page column 91
[2] Patent: WO2013/26914, 2013, A1. Location in patent: Page/Page column 125
[3] Patent: WO2007/103755, 2007, A2. Location in patent: Page/Page column 111
[4] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 20, p. 2925 - 2930
[5] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 24, p. 3161 - 3164
