53995-82-7

基本信息
4,6-DICHLOROINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
ETHYL 4,6-DICHLORO-1H-INDOLE-2-CARBOXYLATE
ETHYL 4,6-DICHLOROINDOLE-2-CARBOXYLATE
ETHYL,4,6-DICLOROINDOLE-2-CARBOXYLATE
物理化學(xué)性質(zhì)
制備方法
![2-[2-(3,5-二氯苯基)肼-1-亞基]丙酸乙酯](/CAS/20210111/GIF/103855-01-2.gif)
103855-01-2

53995-82-7
步驟3:中間體4,6-二氯-1H-吲哚-2-羧酸乙酯(I-ic)的制備 將2-[2-(3,5-二氯苯基)肼-1-亞基]丙酸乙酯(26g,94.50mmol,分兩批次)與多磷酸(260g,每批)在110℃下攪拌反應(yīng)3小時。反應(yīng)完成后,將反應(yīng)混合物緩慢倒入碎冰中,充分?jǐn)嚢韬筮^濾收集沉淀。所得固體用飽和NaHCO3水溶液(調(diào)節(jié)pH至10)堿化,隨后用乙酸乙酯(3×150mL)萃取。合并有機(jī)層,用鹽水洗滌,無水Na2SO4干燥,濃縮。粗產(chǎn)物通過硅膠柱色譜法純化,使用30%乙酸乙酯的己烷溶液作為洗脫劑,得到4,6-二氯-1H-吲哚-2-羧酸乙酯(I-ic)36g,收率73.8%,為灰白色固體。 1H NMR (400 MHz, DMSO-d6): δ 12.46 (s, 1H), 7.46 (s, 1H), 7.30 (s, 1H), 7.12 (s, 1H), 4.36 (q, J = 7.2 Hz, 2H), 1.35 (t, J = 7.2 Hz, 3H)。 ESI MS: m/z 255.8 (M-H)。
參考文獻(xiàn):
[1] Patent: WO2006/109633, 2006, A1. Location in patent: Page/Page column 182-183
[2] Organic Process Research and Development, 2000, vol. 4, # 6, p. 477 - 487
[3] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 4, p. 326 - 330
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 2011, vol. 54, # 10, p. 645 - 656
[5] ACS Infectious Diseases, 2017, vol. 3, # 3, p. 225 - 236