反应 #1563870

ord-61b208f7acdf4b0fa9886a5fa6604814

反应方程式

O=C([O-])[O-].[K+].[K+]
K2CO3
Brc1cn(-c2ccccc2)cn1
4-Bromo-1-phenyl-1H-imidazole
OB(O)c1ccco1
furan-2-ylboronic acid
c1ccc(-n2cnc(-c3ccco3)c2)cc1
4-(furan-2-yl)-1-phenyl-1H-imidazole
收率 21.4%

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤It was then filtered
  2. 2
    洗涤washed with toluene-MeOH (5 ml)
  3. 3
    浓缩the filtrate was concentrated
  4. 4
    其他to yield a crude mixture
  5. 5
    其他column purified

实验过程

4-Bromo-1-phenyl-1H-imidazole (200 mg, 0.9 mmol), furan-2-ylboronic acid (342 mg, 3 mmol), PEPPSI-iPr (18 mg, 0.026 mmol), and K2CO3 (640 mg, 4.64 mmol) were then combined in toluene-methanol (1:1) (4 ml). The reaction mixture was heated under microwave at 80° C. for 20 minutes. It was then filtered and washed with toluene-MeOH (5 ml), and the filtrate was concentrated to yield a crude mixture. The crude mixture was then column purified using 15-20% ethyl acetate/hexanes to afford the desired 4-(furan-2-yl)-1-phenyl-1H-imidazole (50 mg, 0.19 mmol, yield 21.4%) as a brown sticky liquid with an HPLC purity of 95.5%. LC-MS [M+H] 211 (C13H10N2O+H expected 211.08). The 1H-NMR spectra was in accordance with the chemical structure.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09402397B2uspto-grants-2016_08