858116-66-2

基本信息
5-溴-1-(三異丙基硅烷基)-1H-吡咯并[2,3-B]吡啶
N-triisopropylsilyl-5-bromo-7-azaindole
5-Bromo-1-triisopropylsilanyl-7-azaindole
n-Triisopropylsilyl-5-bromo-7-azaindole 98%
5-Bromo-1-(triisopropylsilyl)pyrrolo[2,3-b]pyridine
5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE
(5-Bromopyrrolo[2,3-b]pyridin-1-yl)-triisopropyl-silane
5-broMo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine
5-BROMO-1-TRIISOPROPYLSILANYL-1H-PYRROLO[2,3-B]PYRIDINE-2
(5-bromo-1-pyrrolo[2,3-b]pyridinyl)-tri(propan-2-yl)silane
物理化學性質(zhì)
制備方法

13154-24-0

858116-66-2
以三異丙基氯硅烷為原料合成1-三異丙基硅基-5-溴-7-氮雜吲哚的一般步驟:在室溫條件下,將氫化鈉(0.63 g,25.15 mmol)分批加入到攪拌的5-溴-7-氮雜吲哚(3.3 g,16.75 mmol)的四氫呋喃(THF,50 mL)溶液中,持續(xù)攪拌15分鐘。隨后,加入三異丙基氯硅烷(5.3 mL,25.15 mmol),將反應混合物加熱至80℃并維持3小時。反應完成后,蒸發(fā)除去溶劑,將殘余物溶解于水(50 mL)中。水層用乙酸乙酯(EtOAc,3×50 mL)萃取,有機相用無水硫酸鈉(Na2SO4)干燥后,減壓濃縮。粗產(chǎn)物通過Biotage HPFC系統(tǒng)(洗脫劑:10%乙酸乙酯/己烷)進行純化,得到目標化合物5-溴-1-(三異丙基硅基)-1H-吡咯并[2,3-b]吡啶,為白色固體(5.2 g,收率88%)。質(zhì)譜分析顯示分子離子峰m/z 355(M + 1)。
參考文獻:
[1] Patent: WO2005/103050, 2005, A2. Location in patent: Page/Page column 180
[2] Patent: WO2006/128692, 2006, A2. Location in patent: Page/Page column 158
[3] Patent: US2007/49615, 2007, A1. Location in patent: Page/Page column 62-63
[4] Patent: US2007/49615, 2007, A1. Location in patent: Page/Page column 68