1024598-06-8

基本信息
N-苯基咔唑[1,2]并吲哚
11-苯基吲哚[2,3-A]咔唑
11-苯基吲哚并[2,3-A]咔唑
11-苯基吲哚并[2,3-Α]咔唑
11-苯基-11,12-二氫吲哚并咔唑
12-苯基-11H-吲哚并[2,3-A]咔唑
11-苯基-11,12-氫吲哚并【2,3-A】咔唑
1-苯基-11,12-二氫吲哚并[2,3-A]咔唑
11-苯基-11,12-二氫吲哚并[2,3-A]咔唑
11-phenylindolo[2,3-a]carbazole
12-Phenyl-11H-indolo[2,3-a]carbazole
1,12-Dihydro-11-phenylindolo[2,3-a]carbazole
11-phenyl-11,12-dihydroindolo[2,3-a]carbazole
11,12-Dihydro-11-phenylindolo[2,3-a]carbazole
Indolo[2,3-a]carbazole, 11,12-dihydro-11-phenyl-
11,12-Dihydro-11-phenylindolo[2,3-a]carbazole>
11,12-Dihydro-11-phenylindolo[2,3-a]carbazole
物理化學(xué)性質(zhì)
制備方法

108-86-1
![吲哚并[2,3-A]咔唑](/CAS/GIF/60511-85-5.gif)
60511-85-5
![11,12-二氫-11-苯基吲哚并[2,3-A]咔唑](/CAS/GIF/1024598-06-8.gif)
1024598-06-8
以溴苯和11,12-二氫吲哚并[2,3-a]咔唑為原料合成11,12-二氫-11-苯基吲哚并[2,3-a]咔唑的一般步驟:將Pd2(dba)3(178.6 mg,0.20 mmol)和t-Bu3P(78.9 mg,0.39 mmol)在室溫下于鄰二甲苯(50 mL)中攪拌10分鐘。隨后,加入11,12-二氫吲哚并[2,3-a]咔唑(中間體I-1,5 g,19.51 mmol)、溴苯(3.37 g,21.46 mmol)和t-BuONa(1.12 g,11.71 mmol),并在160℃下回流攪拌48小時。反應(yīng)完成后,冷卻至室溫,加入蒸餾水(20 mL),用乙酸乙酯萃取。有機(jī)相經(jīng)硫酸鎂干燥后,過濾并蒸發(fā)溶劑。通過柱色譜法純化,得到11,12-二氫-11-苯基吲哚并[2,3-a]咔唑(中間體I-2,5.35 g,收率83%)。MS-EI, m/e: 332.13(計算值), 332.19(測量值)。
參考文獻(xiàn):
[1] Patent: KR2015/96018, 2015, A. Location in patent: Paragraph 0377-0379
[2] Patent: US2018/90690, 2018, A1. Location in patent: Paragraph 0161; 0162
[3] Patent: KR2018/32519, 2018, A. Location in patent: Paragraph 0120-0122
[4] Patent: EP2894157, 2015, A1. Location in patent: Paragraph 0198
[5] Patent: KR2015/84657, 2015, A. Location in patent: Paragraph 1642-1645
報價日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價格 |
2025/05/22 | D4860 | 11,12-二氫-11-苯基吲哚并[2,3-a]咔唑 11,12-Dihydro-11-phenylindolo[2,3-a]carbazole | 1024598-06-8 | 200mg | 70元 |
2025/05/22 | XW02102459806804 | 12-苯基-11H-吲哚并[2,3-A]咔唑 | 1024598-06-8 | 5G | 268元 |
2025/05/22 | D4860 | 11,12-二氫-11-苯基吲哚并[2,3-a]咔唑 11,12-Dihydro-11-phenylindolo[2,3-a]carbazole | 1024598-06-8 | 1g | 270元 |