860457-92-7

基本信息
3-溴吲哚-6-甲酸甲酯
3-溴-1H-吲哚-6-羧酸甲酯
1H-吲哚-6-羧酸,3-溴-,甲酯
Methyl 3-broMo-1H-indole-6-carboxylate
3-Bromo-1H-indole-6-carboxylic acid methyl ester
1H-Indole-6-carboxylic acid, 3-bromo-, methyl ester
物理化學(xué)性質(zhì)
制備方法

50820-65-0

860457-92-7
在氮?dú)鈿夥障?,?H-吲哚-6-羧酸甲酯(1.00g,5.71mmol)溶解于無(wú)水DMF(10mL)中。在-60℃下,緩慢滴加N-溴代琥珀酰亞胺(NBS,1.04g,5.84mmol)的無(wú)水DMF(10mL)溶液,滴加時(shí)間超過(guò)20分鐘。反應(yīng)混合物在-60℃下攪拌,隨后在3小時(shí)內(nèi)緩慢升溫至室溫。反應(yīng)完成后,用乙酸乙酯(100mL)和水(20mL,重復(fù)三次)萃取。合并有機(jī)層,真空濃縮除去溶劑。殘余物通過(guò)硅膠柱色譜純化,洗脫劑為石油醚和乙酸乙酯(乙酸乙酯比例從0%開(kāi)始梯度增加),得到3-溴吲哚-6-甲酸甲酯(1.41g,收率98%)。產(chǎn)物經(jīng)1H NMR(600MHz,CD3OD)表征:δ8.15(s,1H),7.80(d,J = 6.0Hz,1H),7.50(m,2H),3.94(s,3H)。
參考文獻(xiàn):
[1] Patent: WO2017/197240, 2017, A1. Location in patent: Page/Page column 204
[2] Patent: WO2009/147121, 2009, A1. Location in patent: Page/Page column 35
[3] Advanced Synthesis and Catalysis, 2018, vol. 360, # 4, p. 626 - 630
[4] Patent: US2005/165049, 2005, A1. Location in patent: Page/Page column 15
[5] Patent: WO2017/184658, 2017, A1. Location in patent: Page/Page column 19; 20