反应 #1563883

ord-f730cec5c4cb489d9467b2226bc30ae6

反应方程式

c1ccc(-c2c[nH]cn2)cc1
4-phenyl-1H-imidazole
Brc1ccco1
2-bromofuran
c1ccc(-c2cn(-c3ccco3)cn2)cc1
1-(furan-2-yl)-4-phenyl-1H-imidazole
收率 7.4%

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The procedure described above in Example 29 for Formula IIc-iii was followed, starting from 4-phenyl-1H-imidazole (250 mg, 1.73 mmol) and 2-bromofuran, to prepare the desired 1-(furan-2-yl)-4-phenyl-1H-imidazole (27 mg, 0.13 mmol, yield 7.4%) as a brownish solid. The HPLC purity of the final product was 99.8%. 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