17759-30-7

基本信息
(4-甲基氨基-2-甲烷磺?;?嘧啶-5-基)-甲醇
(4-(甲基氨基)-2-(甲硫基)嘧啶-5-基)甲醇
4-(MethylaMino)-2-(Methylthio)-5-pyriMidineMethanol
4-(Methylamino)-2-(methylthio)pyrimidine-5-methanol
5-Pyrimidinemethanol, 4-(methylamino)-2-(methylthio)-
(4-MethylaMino-2-MethylsulfanylpyriMidin-5-yl)Methanol
(4-(MethylaMino)-2-(Methylthio )pyriMidin-5-yl)Methanol
(4-MethylaMino-2-Methanesulfanyl-pyriMidin-5-yl)-Methanol
物理化學(xué)性質(zhì)
制備方法

76360-82-2

17759-30-7
以4-甲胺基-2-甲硫基-5-嘧啶甲酸乙酯為原料合成(4-甲基氨基-2-甲烷磺?;?嘧啶-5-基)-甲醇的一般步驟如下:在氬氣保護(hù)下,將氫化鋁鋰(11.48 g,302 mmol)懸浮于裝有頂置式攪拌器的2 L三頸燒瓶中的600 mL無(wú)水四氫呋喃(THF)中。另取250 mL圓底燒瓶,將4-甲基氨基-2-甲硫基-5-嘧啶羧酸乙酯(43.71 g,0.192 mol)溶解于200 mL無(wú)水THF中,并通過套管轉(zhuǎn)移至250 mL加料漏斗中。在室溫下,將嘧啶溶液緩慢滴加至氫化鋁鋰懸浮液中,滴加時(shí)間控制在30分鐘。滴加完畢后,繼續(xù)攪拌反應(yīng)1小時(shí)。隨后,在30分鐘內(nèi)小心滴加25 mL水以淬滅反應(yīng)。接著,依次加入25 mL 15%(w/v)的氫氧化鈉水溶液和75 mL水,此時(shí)反應(yīng)混合物由淺綠色褪色并形成淺綠色漿液,繼續(xù)攪拌1小時(shí)。反應(yīng)完成后,通過真空過濾去除沉淀的鋁鹽,并用乙酸乙酯(EtOAc)充分洗滌固體。將濾液濃縮,得到淺黃色漿液。將該漿液懸浮于250 mL的25% EtOAc/己烷混合溶劑中,通過真空過濾分離無(wú)色固體。經(jīng)真空干燥后,得到31.9 g(產(chǎn)率90%)目標(biāo)產(chǎn)物(4-甲基氨基-2-甲硫基-嘧啶-5-基)-甲醇,其光譜數(shù)據(jù)與文獻(xiàn)報(bào)道一致。
參考文獻(xiàn):
[1] Patent: WO2004/63195, 2004, A1. Location in patent: Page 53-54
[2] Patent: WO2006/71940, 2006, A2. Location in patent: Page/Page column 355
[3] Patent: WO2008/33999, 2008, A2. Location in patent: Page/Page column 88
[4] Journal of Medicinal Chemistry, 2011, vol. 54, # 7, p. 2255 - 2265
[5] Patent: US2003/207900, 2003, A1. Location in patent: Page/Page column 15