54232-43-8

基本信息
6-溴-5-甲氧基皮考啉酸
6-溴-5-甲氧基-2-羧酸吡啶
6-溴-5-甲氧基-2-吡啶甲酸
6-溴-5-甲氧基吡啶-2-羧酸
5-甲氧基-6-溴吡啶-2-甲酸
6-溴-5-甲氧基-2-吡啶羧酸
5-溴-4-甲氧基-2-羧酸吡啶
6-bromo-5-methoxypyridine-2-carboxylicaci
6-bromo-5-methoxypyridine-2-carboxylic acid
2-Bromo-3-methoxypyridine-6-carboxylic acid
6-BROMO-5-METHOXY-2-PYRIDINECARBOXYLIC ACID
2-Pyridinecarboxylic acid, 6-bromo-5-methoxy-
6-Bromo-5-methoxy-2-pyridinecarboxylic acid ,97%
6-Bromo-5-Methoxy-2-Pyridinecarboxylic Acid 6-Bromo-5-Methoxy-2-Pyridinecarboxylic Acid ,97%
物理化學(xué)性質(zhì)
制備方法

24207-22-5

54232-43-8
以2-溴-3-甲氧基-6-甲基吡啶(760 mg,3.76 mmol)為起始原料,將其溶解于15 mL水中。隨后,向該溶液中加入高錳酸鉀(KMnO4,1.49 g,9.40 mmol)。將反應(yīng)混合物在80℃下加熱攪拌3小時(shí)。反應(yīng)完成后,通過薄層色譜(TLC)監(jiān)測反應(yīng)進(jìn)程。用10%鹽酸(HCl)將反應(yīng)混合物的pH值調(diào)節(jié)至4,然后通過硅藻土過濾。濾液用50 mL乙酸乙酯(EA)萃取。有機(jī)層經(jīng)硫酸鎂(MgSO4)干燥后過濾,濃縮濾液,得到5-甲氧基-6-溴吡啶-2-甲酸,為白色固體(665 mg,2.87 mmol,收率75%),產(chǎn)物無需進(jìn)一步純化。1H NMR(400 MHz,DMSO-d6)δ 13.22(s,1H,OH),8.05(d,J = 8.0 Hz,1H),7.60(d,J = 8.0 Hz,1H),4.02(s,3H)。
參考文獻(xiàn):
[1] Journal of Organic Chemistry, 1996, vol. 61, # 14, p. 4623 - 4633
[2] Patent: EP3255042, 2017, A2. Location in patent: Paragraph 0122; 0125
[3] Tetrahedron Letters, 1995, vol. 36, # 30, p. 5319 - 5322
[4] Patent: WO2014/78690, 2014, A1. Location in patent: Paragraph 00201
[5] Patent: WO2016/29214, 2016, A1. Location in patent: Page/Page column 148