Réaction #1563884

ord-b286fd4945cc4b89b84087851d58ebe1

Équation de réaction

Clc1ccc(-c2c[nH]cn2)cc1
4-(4-chlorophenyl)-1H-imidazole
Brc1ccco1
2-bromofuran
Clc1ccc(-c2cn(-c3ccco3)cn2)cc1
4-(4-chlorophenyl)-1-(furan-2-yl)-1H-imidazole
Rendement 1.7%

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-(4-chlorophenyl)-1H-imidazole (125 mg, 0.7 mmol) and 2-bromofuran, to prepare the desired 4-(4-chlorophenyl)-1-(furan-2-yl)-1H-imidazole (3 mg, 0.12, yield 1.7%) as a brownish solid. The HPLC purity of the final product was 95.84%. LC-MS [M+H] 245 (C13H9ClN2O+H expected 245.04). The 1H-NMR spectra was in accordance with the chemical structure.

Source

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