Réaction #1563883

ord-f730cec5c4cb489d9467b2226bc30ae6

Équation de réaction

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
Rendement 7.4%

Réactifs

Aucun

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09402397B2uspto-grants-2016_08