1004294-80-7
1004294-80-7 結(jié)構(gòu)式
基本信息
1-異吲哚酮-6-硼酸頻哪醇酯
1-異吲哚啉酮-6-硼酸頻哪醇酯
6-(四甲基-1,3,2-二噁硼戊環(huán)-2-基)-2,3-二氫-1H-異吲哚-1-酮
6-(4,4,5,5-四甲基-1,3,2-三氧雜戊硼烷-2-基)-異吲哚啉-1-酮
isoindolin-1-one-6-boronic acid pinacol ester
(3-OXOISOINDOLIN-5-YL)BORONIC ACID PINACOL ESTER
1-Oxo-2,3-dihydro-isoindole-6-boronic acid picol ester
1-Oxo-2,3-dihydro-isoindole-6-boronic acid pinacol ester
6-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)isoindolin-1-one
2,3-Dihydro-1H-isoindol-1-one-6-boronic acid pinacol ester
2,3-dihydro-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
(2,3-Dihydro-3-oxo-1H-isoindol-5-yl)boronic acid, pinacol ester
6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one
物理化學(xué)性質(zhì)
制備方法
675109-26-9
73183-34-3
1004294-80-7
以6-溴-2,3-二氫-異吲哚-1-酮和聯(lián)硼酸頻那醇酯為原料合成6-(4,4,5,5-四甲基-[1,3,2]二氧雜硼雜環(huán)戊烷-2-基)-2,3-二氫-異吲哚-1-酮的一般步驟:向6-溴-2,3-二氫-異吲哚-1-酮(1當(dāng)量)的無水二惡烷(0.1M)溶液中加入雙(頻哪醇)二硼(1.1當(dāng)量)、乙酸鉀(3.5當(dāng)量)和1,1'-雙(二苯基膦)二茂鐵(dppf,0.05當(dāng)量)。將反應(yīng)混合物用氮?dú)饷摎?0分鐘。隨后,加入二氯(1,1'-雙(二苯基膦)二茂鐵)鈀(II)(PdCl2(dppf),0.05當(dāng)量),并將混合物再次脫氣5分鐘。在氮?dú)獗Wo(hù)下,將反應(yīng)混合物加熱至70℃反應(yīng)2小時(shí),然后升溫至120℃繼續(xù)反應(yīng)16小時(shí)。反應(yīng)完成后,將混合物在乙酸乙酯(EtOAc)和水之間分配。水相用乙酸乙酯進(jìn)一步萃取,合并有機(jī)相,用硫酸鎂(MgSO4)干燥,過濾后真空濃縮。殘余物用乙酸乙酯超聲處理,懸浮液通過燒結(jié)漏斗過濾,收集的灰色固體干燥后可直接用于下一步反應(yīng),無需進(jìn)一步純化。產(chǎn)物6-(4,4,5,5-四甲基-[1,3,2]二氧雜硼雜環(huán)戊烷-2-基)-2,3-二氫-異吲哚-1-酮的收率為82%,純度為29%,主要雜質(zhì)為硼酸。LC-MS(ESP)分析顯示m/z:519.5 [2M + H]+,保留時(shí)間(R/T)為3.38分鐘。
參考文獻(xiàn):
[1] Patent: WO2008/23161, 2008, A1. Location in patent: Page/Page column 117
[2] Journal of Medicinal Chemistry, 2013, vol. 56, # 23, p. 9542 - 9555
[3] Patent: WO2017/107089, 2017, A1. Location in patent: Page/Page column 37; 38
[4] Patent: WO2017/68412, 2017, A1. Location in patent: Page/Page column 208; 209
[5] Journal of Medicinal Chemistry, 2018, vol. 61, # 11, p. 4978 - 4992
