201677-59-0

基本信息
(R)-N-(2-(芐氧基)-5-(2-溴-1-羥基乙基)苯基)甲酰胺
(R)-N-(2-(芐氧基)-5-(2-溴-1-羥基乙基)苯基)甲酰胺 1KG
Arformoterol Impurity 21
(R)-N-(2-(benzyloxy)-5-(2-bromo-1-hydroxyethyl)phenyl)formamide
(R)-N-[5-(2-Bromo-1-hydroxyethyl)-2-(phenylmethoxy)phenyl]formamide
N-[5-[(1R)-2-Bromo-1-hydroxyethyl]-2-(phenylmethoxy)phenyl]formamide
N-[5-((1R)-2-bromo-1-hydroxyethyl)-2-(phenylmethoxy)phenyl]carboxamide
Formamide,N-[5-[(1R)-2-bromo-1-hydroxyethyl]-2-(phenylmethoxy)phenyl]-
物理化學(xué)性質(zhì)
制備方法

64-18-6

188690-82-6

201677-59-0
一般步驟:向Parr氫化釜中加入PtO2催化劑和溶解于混合溶劑THF(25 mL)與甲苯(25 mL)中的(R)-1-(4-芐氧基-3-硝基苯基)-2-溴乙醇(3.60 g,10.22 mmol)。在氫氣氛圍下,于室溫、55 psi壓力下振蕩反應(yīng)14小時(shí)。反應(yīng)完成后,釋放氫氣壓力。向反應(yīng)混合物中直接加入甲酸(0.65 mL,17.23 mmol)和乙酸酐(1.10 mL,11.65 mmol)的混合液。將新形成的混合物在室溫下繼續(xù)攪拌16小時(shí)。反應(yīng)結(jié)束后,通過硅藻土墊過濾以移除催化劑,濾液經(jīng)旋轉(zhuǎn)蒸發(fā)濃縮。所得殘余物通過柱色譜法(硅膠為固定相,洗脫劑為30:70至50:50的乙酸乙酯/己烷梯度)進(jìn)行純化,得到目標(biāo)產(chǎn)物(R)-N-(2-(芐氧基)-5-(2-溴-1-羥基乙基)苯基)甲酰胺(5),為白色固體(3.62 g,收率>99%)。產(chǎn)物結(jié)構(gòu)經(jīng)1H NMR(300 MHz,CDCl3)確認(rèn):δ 2.95(s,1H),3.52(m,1H),3.60(m,1H),4.85(m,1H),5.08(s,2H),6.96(d,1H),7.13(dd,1H),7.39(m,5H),7.88(br s,1H),8.37(dd,1H)。
參考文獻(xiàn):
[1] Patent: WO2007/146867, 2007, A2. Location in patent: Page/Page column 51-52
[2] Patent: US2011/275623, 2011, A1. Location in patent: Page/Page column 27