433226-06-3
433226-06-3 結(jié)構(gòu)式
基本信息
Ethyl 2-amino-5-bromopyridine-3-carboxylate
3-Pyridinecarboxylic acid, 2-aMino-5-broMo-, ethyl ester
Ethyl 2-amino-5-bromopyridine-3-carboxylate, 2-Amino-5-bromo-3-(ethoxycarbonyl)pyridine
物理化學(xué)性質(zhì)
安全數(shù)據(jù)
制備方法
13362-26-0
433226-06-3
以2-氨基煙酸乙酯為原料合成2-氨基-5-溴煙酸乙酯的一般步驟:在0℃下,向攪拌的2-氨基煙酸乙酯(15g; 90.36mmol; 1當(dāng)量)的無水THF(150mL)溶液中分批加入N-溴代琥珀酰亞胺(NBS)(16g; 90.36mmol; 1當(dāng)量)。將得到的混合物在23℃下攪拌18小時(shí)。反應(yīng)完成后,將混合物倒入冰冷的飽和NaHCO3水溶液中,用乙酸乙酯(3×200mL)萃取有機(jī)組分。合并的有機(jī)層用鹽水溶液洗滌,用無水硫酸鈉干燥,過濾并減壓濃縮至干,得到2-氨基-5-溴煙酸乙酯(22g,100%),為灰白色固體。產(chǎn)物經(jīng)1H NMR(DMSO-d6)確認(rèn):δ 8.29(d, 1H, J = 3Hz),8.12(d, 1H, J = 2Hz),7.31(s, 2H),4.29(q, 2H, J = 7Hz),1.30(t, 3H, J = 7Hz)。LCMS分析結(jié)果:m/z = 245.0 [M + H]+, 247.0 [M + 2H]+, 保留時(shí)間(RT)= 3.34分鐘(程序P1,柱W)。
參考文獻(xiàn):
[1] Patent: WO2015/95128, 2015, A1. Location in patent: Paragraph 0239; 0242; 0243
[2] European Journal of Medicinal Chemistry, 2018, vol. 158, p. 236 - 246
[3] Patent: CN104402881, 2016, B. Location in patent: Paragraph 0022; 0023
[4] Patent: WO2007/67416, 2007, A2. Location in patent: Page/Page column 64; 134
