486422-08-6

基本信息
3-(4,4,5,5-四甲基-1,3,2-二噁硼戊環(huán)-2-基)苯磺酰胺
BENZENESULFONAMIDE-3-BORONIC ACID PINACOL ESTER
3-aMinosulfonyl-phenylboronic acid pinacol ester
3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1-sulfonamide
3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonaMide
Benzenesulfonamide, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
物理化學(xué)性質(zhì)
制備方法

89599-01-9

73183-34-3

486422-08-6
以3-溴苯磺酰胺(0.620 g,2.63 mmol)、醋酸鉀(KOAc,1.032 g,10.52 mmol)和PdCl2(dppf)2(0.100 g,0.137 mmol)為原料,在氬氣保護(hù)下,將其溶于二惡烷(20 mL)中,鼓泡氬氣10分鐘以除氧。隨后,向反應(yīng)體系中加入雙(頻哪醇合)二硼(1.000 g,3.94 mmol),密封反應(yīng)容器,于110℃下攪拌反應(yīng)24小時(shí)。反應(yīng)完成后,將混合物冷卻至室溫,通過硅藻土過濾。濾液經(jīng)減壓濃縮后,殘留物通過硅膠柱層析純化(洗脫劑:石油醚/乙酸乙酯,梯度從4:1至1:1),得到目標(biāo)產(chǎn)物3-(4,4,5,5-四甲基-1,3,2-二氧雜硼雜環(huán)戊烷-2-基)苯磺酰胺(0.663 g,收率89%)為白色固體。產(chǎn)物經(jīng)NMR(DMSO-d6,HMDSO)表征:δ 8.14(ddd,J = 2.0, 1.1, 0.5 Hz,1H),7.93(ddd,J = 7.9, 2.0, 1.3 Hz,1H),7.85(td,J = 1.2, 7.4 Hz,1H),7.59(ddd,J = 7.9, 7.4, 0.5 Hz,1H),1.32(s,12H)。LCMS(ESI)m/z:284.0 [M + H]+。
參考文獻(xiàn):
[1] Patent: WO2016/129983, 2016, A1. Location in patent: Page/Page column 35
[2] Patent: US2016/318895, 2016, A1. Location in patent: Paragraph 0339