76240-49-8

基本信息
6-溴二氮雜萘-1,4-二醇
6-溴-2,3-二氫酞嗪-1,4-二酮
1(2H)-PHTHALAZINE, 7-BROMO-4-HYDROXY
1(2H)-Phthalazinone, 7-bromo-4-hydroxy-
6-Bromo-2,3-dihydrophthalazine-1,4-dione
物理化學(xué)性質(zhì)
制備方法

86-90-8

76240-49-8
以5-溴異苯并呋喃-1,3-二酮為原料合成6-溴酞嗪-1,4-二醇的一般步驟如下:將4-溴鄰苯二甲酸酐(50g,0.22mol)溶于乙酸(150mL)中,攪拌并在125℃下加熱1小時。反應(yīng)完成后,將混合物冷卻至室溫,隨后在5分鐘內(nèi)緩慢滴加水合肼(11.25mL,0.23mol),此時觀察到濃稠白色固體的形成。繼續(xù)加入乙酸(50mL),并將混合物在125℃下再次加熱30分鐘。反應(yīng)混合物冷卻后,用乙酸(200mL)稀釋,并進(jìn)行過濾。濾餅用乙酸(3×100mL)洗滌,隨后在真空條件下干燥。將干燥后的固體溶解于5%(w/w)NaOH溶液(250mL)中,用乙酸(30mL)酸化懸浮液,產(chǎn)生濃稠的白色沉淀。過濾該混合物,濾餅依次用水(2×200mL)和甲醇(2×200mL)洗滌,最后在40℃下真空干燥,得到白色固體6-溴-2,3-二氫酞嗪-1,4-二酮(55g,0.23mol,產(chǎn)率定量)。產(chǎn)物結(jié)構(gòu)通過1H NMR(300MHz,DMSO-d6)確認(rèn):δ= 8.16(dd,J = 0.7,2.0Hz,1H),7.98(dd,J = 0.7,8.4 Hz,1H),7.93(d,J = 8.4 Hz,1H),1.84(s,2H)。
參考文獻(xiàn):
[1] Patent: WO2016/92326, 2016, A1. Location in patent: Paragraph 00326
[2] Angewandte Chemie - International Edition, 2007, vol. 46, # 10, p. 1684 - 1687
[3] Patent: WO2008/61108, 2008, A2. Location in patent: Page/Page column 65-66
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980, p. 1834 - 1840
[5] Patent: WO2004/99177, 2004, A1. Location in patent: Page 19-20